מנהל עבודה לחברה יזמית קבלנית מובילה בתל אביב שכר 30 אלף + רכב!!! משרה מס’ 55318 תיאור משרה תכנון וניהול אתר מקצה לקצה, משאבי ציוד הנדרשים לביצוע הפרויקט בהתאם ללוז, לתקציב ולבטיחות. לרבות הזמנת חומרים עפ”י צורך ותוך חישוב ותכנון מקדים. אחריות לבטיחותם של העובדים והמבקרים באתר, תוך קיום שגרת “בטיחות” והקפדה על נהלי החברה ודרישות החוק. ניהול משימות יומי ושבועי בהתאם לנתיב הקריטי של הפרויקט. פתיחת מלאכות בצורה מסודרת, קבלת עבודה בסיום מקבלני המשנה תוך בקרת איכות באופן שוטף בכלל המלאכות. חניכה וניהול יעיל של הקבלנים והפועלים לעמידה באיכות, בלו”ז ובתקציב. היצמדות למפרטי יועצים ופרטי חברה. דרישות הסמכה כמנהל עבודה מוסמך חובה. ניסיון כמנהל עבודה בתחום השלד והגמרים במבני מגורים לפחות 5 שנים חובה. יכולת קריאת תוכניות מעולה חובה. שליטה מלאה בעברית חובה. שליטה בישומי מחשב חובה. יחסי אנוש טובים חובה. הנדסאי /ת בניין יתרון. עבודה קודמת בת”א יתרון. אחריות אישית גבוהה, אסרטיביות, חריצות, אמינות וקפדנות. המשרה מיועדת לנשים ולגברים כאחד לפרטים נוספים ובדיקת התאמה יש לשלוח קורות חיים ל: חובה לציין מספר משרה 55318

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מתויג כ: הנדסאי

^^משרה זו נלקחה מ Career^^Centene is transforming the health of our communities one person at a time. As an Executive on our team, you could be the one who changes everything for our 28 million members. Must reside in Iowa, Missouri, Kansas, Nebraska. Relocation assistance available Position Purpose: Oversee all related activities for the Quality Improvement functions. Lead and direct process improvement activities for more efficient and streamlined workflow. Oversee the business processes related to risk adjustment and quality improvement for assigned products and plans. Responsible for all activities related to National Committee for Quality Assurance (NCQA) Accreditation and/or Healthcare Effectiveness Data and Information Set (HEDIS) performance ensuring highest level of accreditation and health plan rating. Manage all aspects of HEDIS improvement activities, including outreach, incentives, data integrity and chart review. Responsible for insuring no loss of revenue due quality performance related to state contracts either through Pay for Quality program or liquidated damages due not hitting dashboard measures. Responsible for managing member engagement vendor including the setting of performance standards and monitoring of performance standards. Review and implement new technological tools and processes and foster team concept with internal and external constituencies. Present results of improvement efforts and ongoing performance measures and recommend actions plans to senior management. Manage and ensure compliance of Early and Periodic Screening, Diagnostic and Treatment (EPSDT) program as well as compliance and turnaround time of quality of care reviews. Responsible for all activities related to risk adjustment performance ensuring highest level of return. Formulate and establish policies, operating procedures, and goals in compliance with internal and external guidelines. Responsible for all activities related to Risk Adjustment performance including outreach and chart review to ensure highest level of return. Participate in, attend and plan/coordinate staff, departmental, committee, sub
• committee, community, State and other activities, meetings and seminars. Work collaboratively with Provider Performance to support the expansion of alternative payment models using HEDIS data. Performs other duties as assigned. Complies with all policies and standards. Education/Experience: Master’s Degree in Nursing or related clinical field or equivalent experience required. 10+ years of experience managing acquisition and integration of external data sources required. Previous management experience including responsibilities for hiring, training, assigning work and managing performance of staff. Familiarity with running risk adjustment prospective and retrospective programs preferred. RN license and Certified Professional in Health Care Quality preferred. Or equivalent experience acquired through accomplishments of applicable knowledge, duties, scope and skill reflective of the level of this position. Pay Range: $213,300.00
• $403,700.00 per year Centene offers a comprehensive benefits package including: competitive pay, health insurance, 401K and stock purchase plans, tuition reimbursement, paid time off plus holidays, and a flexible approach to work with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an individual’s skills, experience, education, and other job
• related factors permitted by law, including full
• time or part
• time status. Total compensation may also include additional forms of incentives. Benefits may be subject to program eligibility. Centene is an equal opportunity employer that is committed to diversity, and values the ways in which we are different. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristic protected by applicable law. Qualified applicants with arrest or conviction records will be considered in accordance with the LA County Ordinance and the California Fair Chance Act Thanks for your interest in Centene and its subsidiary companies. We’re so glad that you’ve decided to fill out an application and take the next step to find your purpose. Also, we’re here to help support you on your candidate journey. Should you need an accommodation, please email recruiting@centene.com. Centene is committed to helping people live healthier lives. We provide access to high
• quality healthcare, innovative programs and a wide range of health solutions that help families and individuals get well, stay well and be well.

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for hiring, training, assigning work and managing performance of staff. Familiarity with running risk adjustment prospective and retrospective programs preferred. RN license and Certified Professional in Health Care Quality preferred. Or equivalent experience acquired through accomplishments of applicable knowledge, duties, scope and skill reflective of the level of this position. Pay Range: $213,

^^משרה זו נלקחה מ Career^^Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr
• accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions. Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University’s career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following: Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required. Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application. Job Title: Lead Clinical Research Coordinator Department: Medicine | Neurological Surgery Lead Clinical Research Coordinator serves as primary resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the non
• cancer Center for Clinical Research Management (CCRM) for the Department of Neurological Surgery; plans, implements & oversees daily conduct of protocol activities; serves as primary reviewer of patient records to assess & identify patients who meet criteria for participation in research studies; recruits, interviews & promotes study to eligible patients; educates patients and families of purpose, goals, & processes of clinical study; leads patient enrollment activities & ensures informed consent authorization is obtained & administered in compliance to regulatory & sponsor requirements; facilitates collection, processing & evaluation of biological samples, as well as scheduling and follow
• through of patient care appointments, procedures, & other diagnostic testing; monitors patients for adverse reactions to study treatment or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in collecting, extracting, coding, & analyzing clinical research data; monitors & ensures compliance with Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state & industry sponsor regulations; participates in planning and preparing for external compliance, quality assurance & control reviews; participates in development of new research protocols and contributes to planning of goals to meet study requirements; works closely with principal investigators upon awarding of new protocols and recommends team assignments; assists with preparation and submission of publications, research reports, and grant proposals; trains, mentors, approves timesheets, assists with annual Buckeye Performance goals and performance, and supervises staff. Education Required Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required. Experience Required 3
• 5 years’ experience in a clinical research capacity conducting clinical research studies required. Computer skills required. Required Certification Clinical research certification from an accredited certifying agency required (ACRP or SOCRA). The certification must be maintained while in this role. Preferred Education and Experience 5 years of relevant experience required. 6
• 8 years of relevant experience preferred. Experience in a progressively responsible management capacity in a medical research environment preferred. Experience with neurological disorders is preferred. Requires successful completion of a background check. Qualified candidates may be requested to complete a pre
• employment physical, including a drug screen. FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research CAREER BAND: Individual contributor
• Specialized CAREER LEVEL: S4 Additional Information: Location: Starling Loving Hall (0176) Position Type: Regular Scheduled Hours: 40 Shift: First Shift Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process. Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions. The university is an equal opportunity employer, including veterans and disability. As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression. Each day, Buckeyes across the state and around the world make a lasting impact. The Ohio State University sets the stage for academic achievement and innovation. It’s where friendships are forged, tradition is brought to life and a better global community is built. Our mission is as clear today as it was 150 years ago: to illuminate a pathway to education, research and health care that creates vibrant futures. Faculty and staff build the incomparable Buckeye spirit through collaboration, a strong sense of community and an unwavering commitment to excellence. Our strength comes from our ability to bring out the best in people and learn from Buckeyes of all backgrounds, passions and talents. Ohio State is a dynamic community where opportunity thrives and individuals transform themselves and their world. Positions are available in countless fields and specialties. Ohio State is a top
• 20 public university, and its Ohio State Wexner Medical Center is one of America’s leading academic health centers. Eligible Ohio State employees receive comprehensive benefits packages, including medical, dental and vision insurance, tuition assistance for employees and their dependents, and state or alternative retirement options with competitive employer contributions. Become a Buckeye and contribute to an incredible legacy that serves to guide our future and shape a better tomorrow.

דרישות המשרה

; facilitates collection, processing & evaluation of biological samples, as well as scheduling and follow
• through of patient care appointments, procedures, & other diagnostic testing; monitors patients for adverse reactions to study treatment or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of

^^משרה זו נלקחה מ Career^^At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function: Supply Chain Engineering Job Sub Function: Quality Engineering Job Category: Scientific/Technology All Job Posting Locations: Yokneam, Haifa District, Israel Job Description: About Cardiovascular Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent for NPD Quality Engineer to be in Yokneam. As a NPD Quality Engineer, you will be responsible for NPI products transfer from development to production, validation activities , supporting activities related to process and production quality improvements, non
• conforming products process management The Quality Engineer is mainly responsible for: Leading NPI product transfer from development to production Manage process validation, including supplier guidance. Manage Supplier related activities ( Review and approve supplier nonconformance, Investigations and lead improvement plans with the suppliers) Manage activities related to nonconformance methodology (nonconformance follow up and reports, and product dispositions). Experience with validations (IQ/OQ/PQ/TMV) and supplier management Conduct and support NC investigations (internal and supplier non
• conformances). Performing analysis of nonconforming products and presenting data in monthly meetings. Support the production team in analyzing and reporting the quality event. Qualifications: BSc in Engineering/ BA degree or Practical Engineering with Qualification in Quality Assurance (CQE). At least 5 years experience in medical systems or medical device companies Knowledge of investigations & cause analysis. Demonstrated knowledge of manufacturing process principles, practices, and procedures. Leading multidisciplinary project and processes Good communication skills, both verbal and written in English. Good interpersonal relations, reliable and accurate, sense of urgency, and a team player. #LI
• Hybrid #LI
• LM5 At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. Do Not Sell or Share My Personal Information Limit the Use of My Personal Information

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BSc in Engineering/ BA degree or Practical Engineering with Qualification in Quality Assurance (CQE). At least 5 years experience in medical systems or medical device companies Knowledge of investigations & cause analysis. Demonstrated knowledge of manufacturing process principles, practices, and procedures. Leading multidisciplinary project and processes Good communication skills, both verbal and

^^משרה זו נלקחה מ Career^^Your mission The IFGD Project and Policy Officer is responsible for supporting the coordination and execution of projects and revision of policies within the mandate of IFGD, ensuring the continuous improvements of Institutional Fundraising and Grant Management processes within WCAF and across the Alliance. The role includes three complimentary functions: Continued support to IFGD Systems & Processes, Project & policy coordination and execution, Institutional funding account management support. The role is expected to adapt and evolve in line with the AP2026 planning process and wider organizational planning process. This role involves approximately 40% focusing on project and policy support, 20% coordination and 60% on account manager supporting departments as indicated by the Head of IFGD. Your profile 1. Support to the IFGD Systems & Processes Team Contribute to grants data processes (e.g., grants and partner funding agreement activations), ensuring compliance with internal controls and donor guidelines. Collaborate directly with programme colleagues (CO, Global, etc.) to support their effective use of Rafiki, ensuring data is entered accurately and in a timely manner. Coordinate the Bid Committee, monitor the dedicated inbox, and serve as the point of contact by presenting items for discussion to the Bid Committee members. Support team leads in identifying and analysing trends, challenges, and developments within IFGD and related areas, and in translating insights into actionable improvements for work processes, tools, systems, and policies. Support with active input in the continuing process of institutional fundraising and grant management quality improvement for the purpose of the service within the project area, including processes and system optimization. 2. Support with Institutional Fundraising and Grant Management project & policy execution and coordination (30%) Working directly with the Head of IFGD and/or S&P Team leads, reviews policies, guidelines and procedures related to IFGD area of work in donor relations & institutional fundraising and quality assurance that have been already developed to identify problems/deviations and put forward suggested improvements and prepare project briefs for such revisions. Share information and organize training and/or roll out sessions to support the roll out of new or reviewed policies and procedures related to IFGD area of work in donor relations & institutional fundraising and quality assurance. Works with Head of IFGD and wider WCAF and Alliance collaboration mechanisms to support timely and accurate coordination of policy and project information, and timely management of information related to the relevant coordination mechanisms (IF ACG, policy committee etc.). 3. Donor and Partnership Management: INGO institutional account management support Work in coordination with the Head of IFGD and/or Sub
• team leads to support the IF management of key relationships with INGO and other partners (e.g. for R&D), including supporting teams with identifying grant opportunities. Work in coordination with Account Managers and Department leads and monitor trends, partner & donor priorities, and translate these into actionable plans in support of ongoing fundraising efforts. Support designated project and/or Rafiki leads with registration, updates, and agreements for opportunities with INGOs and R&D partners. Ensure INGO partner relationships and opportunities data is provided to the Alliance (both by FMs and WCAF departments) through use of existing systems & processes, ensuring a coordinated approach. Support senior team leads collaboration with the finance team to ensure accurate financial tracking and compliance for grant activities across the INGO, and any other portfolios as required. Experience, Knowledge & Skills University degree Experience in the humanitarian context, preferably with institutional funding and grant management cycle Strong analytical skills to identify and solve problems Capacity building capabilities in order to roll out policies, procedures and guidelines, conveying complex concepts in a simple and understandable manner Ability to adapt to changing priorities, market conditions, and organizational needs, while maintaining focus on achieving institutional foundations goals Proficiency in computer skills, especially in MS Office (Excel, Outlook, Word, PowerPoint, Teams etc.) Strong abilities in promoting an organizational culture that prioritizes respect, fairness, and ethical treatment of all stakeholders, contributing to a safe and inclusive work environment A critical and logical thinker helping to identify underlying principles, reasons, or facts Ability to effectively communicate in English and preferably in any other WCA languages What we offer Location : We work with global teams with team members being based in different locations. War Child is currently operates in: Afghanistan, the Central African Republic, Colombia, DR Congo, Germany, Jordan, Lebanon, the occupied Palestinian territory, South Sudan, Sweden, Syria, Uganda, Ukraine (soon to be registered), and Yemen. We also have offices in the Netherlands and the United Kingdom. Preference is given to applicants who reside and have valid working permits. War Child does not offer relocation nor visa sponsorship. Type of Contract : Local contract with salary and secondary labour conditions based on the in
• country salary scale, local T&C’s will apply. Professional Development: Opportunities for capacity building and growth, both within the role and through War Child’s broader network. Meaningful Impact: The chance to make a tangible difference in the lives of children and families affected by conflict, contributing to long
• term, sustainable change. Equal Opportunities: War Child is an inclusive employer committed to diversity and inclusion, respecting all individuals regardless of age, gender, religion, ethnicity, nationality, or physical ability. Workplace Culture: War Child is dedicated to fostering a diverse, inclusive, and respectful workplace that prioritizes safety and fairness for all individuals. We strictly prohibit any form of discrimination, harassment, retaliation, or bullying within our organization Why You Should Apply Make a Real Impact: Your work will directly contribute to providing quality education to children who need it most, creating lasting change in their lives. Career Growth: Join a dynamic organization that values your professional development and offers opportunities for learning, growth, and innovation. Global Reach: Play a key role in scaling a ground
• breaking programme that operates in multiple conflict
• affected regions around the world. Collaborative and Mission
• Driven: Work alongside passionate colleagues and partners united in a mission to protect children and help them thrive despite adversity. How to Apply Qualified candidates are encouraged to submit their applications (CV& motivation letter in English) by November 10, 20
25. . We are reviewing submissions on a rolling basis, so early applications are strongly recommended. ________________________________________________________________________________ By submitting your application you certify that all of the statements made in your application are true, complete, and correct and are made in good faith. You understand that falsifying, misrepresenting or intentionally withholding information will be grounds for rejection of your application or withdrawal of any offer of appointment or, if an appointment offer has been accepted, this will be ground for employment sanctions, such as, but not limited to, instant dismissal. In addition, you understand that you need to submit a Criminal Record Certificate and that, if you fail to submit it, no employment relationship can be established. War Child is an international organisation, and we are committed to be a diverse and inclusive employer, placing human and child rights at the centre of our existence and work. We hire our new colleagues based on their talents, competences and shared values; we do not distinguish them based on their age, gender and gender identity, race, color, ethnicity, religion, culture, sexual orientation, disability etc. The safety of children and youth is a paramount and essential to War Child’s work. War Child has a zero tolerance policy towards any form of abuse. To prevent placing children and youth at any risk this subject is addressed in our recruitment and selection procedures. Moreover, the accepted candidates will be required to state their commitment/ intent to be aware, consider and adhere to the minimum standards applicable in development and humanitarian settings, such as humanitarian values and principles, Sphere Humanitarian Charter, Standards in the Humanitarian Standards Partnership, Core Humanitarian Standard, International Humanitarian Law, Code of Conduct for the International Red Cross and Red Crescent Movement and Non
• Governmental Organizations (NGOs) in Disaster Relief and IASC Six Core Principles Relating to Sexual Exploitation and Abuse. Disclaimer Only applications received via our website are processed. If we appoint a suitable candidate before the given closing date, we reserve the right to remove the vacancy from our website before that date. In such a case, any responses received after that time are not processed. It could be that during our selection process the closing date for the vacancy is extended. If so, and you have not yet heard from us, your application will remain active.

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לא צויין

^^משרה זו נלקחה מ Career^^Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr
• accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions. Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University’s career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following: Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required. Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application. Job Title: Office Services Senior Coordinator
• Surgical Pathology Consultation Office Department: Medicine | Pathology Position Summary Under the direction of the Pathology Support Services Manager, assists with the daily administrative, accessioning, and office duties in the Division of Surgical Pathology Consultation Office; receives and logs non
• OSU pathology cases (slides, paraffin tissue blocks, outside pathology report) for 2nd opinion diagnosis; ensures receipt of written documentation for consultation from the ordering physician; ensures receipt of patient’s 3rd party payer information for accuracy in billing; uses IHIS to register patients and order a consultation case; assists the pathologist when indicated by ordering additional special stains, IHC stains, molecular pathology and specialty testing associated with the 2nd opinion; organizes consult slides, blocks and accompanying paperwork; maintains quality assurance spreadsheets; operates computer equipment to produce complex and confidential medical reports, correspondence and documents; answers phones and responds to inquiries from department and medical center staff, pathologists, clinicians, physicians, researchers and attorneys; researches, compiles and analyzes materials; produces mailings for patient consultation reports; returns outside blocks and slides periodically and according to retention policies; works closely with OSU medical center personnel to ensure timely communications to complete accessioning process for patients scheduled for OSU medical center appointments; works closely with pathology core facility staff to ensure accurate accessioning of molecular pathology cases; directs student employees to provide assistance with office tasks and frequent delivery of case to/from the pathologists or to/from the histology lab. Job Requirements High School diploma or GED. 2 years of relevant experience required. Additional Information: Location: Doan Hall (0089) Position Type: Regular Scheduled Hours: 40 Shift: First Shift Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process. Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions. The university is an equal opportunity employer, including veterans and disability. As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression. Each day, Buckeyes across the state and around the world make a lasting impact. The Ohio State University sets the stage for academic achievement and innovation. It’s where friendships are forged, tradition is brought to life and a better global community is built. Our mission is as clear today as it was 150 years ago: to illuminate a pathway to education, research and health care that creates vibrant futures. Faculty and staff build the incomparable Buckeye spirit through collaboration, a strong sense of community and an unwavering commitment to excellence. Our strength comes from our ability to bring out the best in people and learn from Buckeyes of all backgrounds, passions and talents. Ohio State is a dynamic community where opportunity thrives and individuals transform themselves and their world. Positions are available in countless fields and specialties. Ohio State is a top
• 20 public university, and its Ohio State Wexner Medical Center is one of America’s leading academic health centers. Eligible Ohio State employees receive comprehensive benefits packages, including medical, dental and vision insurance, tuition assistance for employees and their dependents, and state or alternative retirement options with competitive employer contributions. Become a Buckeye and contribute to an incredible legacy that serves to guide our future and shape a better tomorrow.

דרישות המשרה

High School diploma or GED. 2 years of relevant experience required. Additional Information: Location: Doan Hall (0089) Position Type: Regular Scheduled Hours: 40 Shift: First Shift Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process. Thank you for your interest in positions at The Ohio State Universit

^^משרה זו נלקחה מ Career^^Description Core Mission The Sales specialist will treat all drivers from lead stage till activation and onboarding. The Sales Specialist will be responsible for all converted drivers working with ‘Gett drivers app’ while maintaining a high quality drivers fleet. Responsibilities: Responsible for the full sales cycle to the Drivers: lead conversation; data validation; identifying the driver’s needs; suggesting the best package and closing deals by a monthly target. The role will also include drivers training as a part of the deal closing and quality assurance and initial follow
• ups and possible outbound activities. Requirements At least 2
• 3 year experience in B2C Telemarketing /Sales Managing sales process via Sales force
• advantage High negotiating capabilities Ability to create outbound Working independently based on targets and goals Ability to gain trust and confidence with the different customers Ability to adjust quickly to a changing environment Strong ”can do” approach Strong oral and written communication skills At Gett, we’re committed to creating an inclusive, respectful environment where everyone feels valued and empowered to succeed. We believe that diversity drives innovation, and we’re proud to offer equal opportunities to all
• regardless of age, race, gender identity, sexual orientation, disability, or any other characteristic. If you need accommodations during the recruitment process, please contact us at recruitment.il@gett.com ,and we’ll do our best to support you. Click here to view our privacy policy. תיאור משרה None Requirements in local language None

דרישות המשרה

Responsible for the full sales cycle to the Drivers: lead conversation; data validation; identifying the driver’s needs; suggesting the best package and closing deals by a monthly target. The role will also include drivers training as a part of the deal closing and quality assurance and initial follow
• ups and possible outbound activities. Requirements At least 2
• 3 year experience in B2C Telema

# ** מנהל/ת עבודה בגמרים לפרויקטים ציבוריים בירושלים!** במסגרת התפקיד: ניהול שוטף של עבודות הגמר (ריצוף, טיח, צבע, תקרות אקוסטיות, נגרות, אלומיניום, מערכות גמר וכדומה), פיקוח על קבלני משנה וספקים באתר, כולל תיאום בין כל הגורמים, עמידה בדרישות התקינה הציבורית (ת”י משרד החינוך, משרד הבריאות וכ”ו), תכנון ובקרה על לו”ז שלב הגמרים, כולל הכנת תשתיות מקדימות, בקרת איכות קפדנית ובדיקת התאמה לתוכניות עבודה ולמפרטים טכניים, פתרון בעיות בשטח ותיאום מול יועצים ומתכננים במידת הצורך, הכנת האתר למסירות, ביצוע רשימות ליקויים וליווי תיקונים עד למסירה מלאה, הקפדה על בטיחות בעבודה בהתאם לחוק ונהלים פנימיים. ימים ושעות העבודה: א’ ה’ 16:00 8:0. מוכנות לשעות נוספות לפי הצורך. שכר: 25,000 ש”ח. תלוי ניסיון. דרישות: מנהל/ת עבודה מוסמך/ת בעל ניסיון מוכח 10 שנים לפחות בניהול וביצוע פרויקטים של מבנים עתירי מערכות. לפחות 2 פרויקטים שהושלמו במהלך 10 שנים האחרונות בהיקף ביצוע מצטבר שלא יפחת מ 100 מיליון. אחראי/ת על הבטיחות ויהיה רשום/ה במשרד העבודה. תעודת מנהל/ת עבודה מוסמך/ת חובה. הנדסאי/מהנדס/ת בניין יתרון. יכולת ניהול גבוהה, סדר וארגון, תקשורת בין אישית טובה. למעוניינים, נא לשלוח קורות חיים למייל ולציין “מנהל/ת עבודה גמרים בירושלים.’ בהצלחה! אם זה לא בשבילך שלח/י לחבר/ה שזה בול בשבילם!

דרישות המשרה

דרישות התקינה הציבורית (ת”י משרד החינוך, משרד הבריאות וכ”ו), תכנון ובקרה על לו”ז שלב הגמרים, כולל הכנת תשתיות מקדימות, בקרת איכות קפדנית ובדיקת התאמה לתוכניות עבודה ולמפרטים טכניים, פתרון בעיות בשטח ותיאום מול יועצים ומתכננים במידת הצורך, הכנת האתר למסירות, ביצוע רשימות ליקויים וליווי תיקונים עד למסירה מלאה, הקפדה על בטיחות בעבודה בהתאם לחוק ונהלים

מתויג כ: הנדסאי

We are Growing! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization. Biorasi is looking for top performers who are as passionate about clinical research as we are – clinical trial veterans and industry newcomers who will thrive in our fast-paced environment and help us drive new therapies to patients. Here is your chance to become a vital part of a growing global company in the expanding clinical research industry. Your Role * Schedule, Plan and Conduct Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. * Write Reports and Investigator Follow-up Letters for Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. * Manages the progress of assigned studies by tracking regulatory/ IRB submissions and approvals, recruitment and enrolment, CRF completion and submission, and data query generation and resolution * Provide project updates to project management team. * Organize delivery of investigational product, laboratory supplies, CRFs and other study specific materials to and from the clinical sites. * Perform investigational product inventory and ensure return of unused investigational product to designated location or verify destruction as required. * Assists with, prepare for, and attends Investigator Meetings for assigned studies. * Review study documents for compliance with protocol, ICH GCP guidelines, Protocol Deviations/Violations and Waivers, review study documents for subject safety events; escalate issues at site to project management. * Collect and review essential study documents from site for filing in eTMF. * Administers protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues. * Evaluates quality and integrity of study site practices related to the proper conduct of the study and ensure adherence to applicable regulations. * Compliances: Follow international GCP guidelines/regulations and SOPs for executing clinical studies. Participates in the planning of quality assurance activities and coordinates resolution of audit findings. * Assists the Clinical Trial Manager with clinical operations activities by overseeing resource allocation, reviewing site performance, providing feedback to CRAs and CTAs, resolving issues, performing review and oversight of site visit reports. * May review protocols, eCRFs, study manuals and other study related documents, as requested by the Clinical Trial Manager. * May conduct on-site evaluation visits and on-site training of CRAs * Lead and partake in regular team meeting / teleconferences. * Assist, as appropriate, with reporting site performance regarding timelines and deliverables during project team meetings and assist with providing and compiling feedback for analysis of overall study performance. * May serve as mentor to associates on the subject of job performance, trainings and professional growth. * Other duties as assigned. Your Profile * Bachelor’s Degree in biomedical sciences or related scientific discipline * Fluent English (oral and written) and applicable local business language. * Minimum three years of monitoring experience, more experience preferred, with a combination of clinical research coordinator and or other relevant clinical research experience. * Sound knowledge of medical terminology and advanced proficiency in clinical monitoring process. * Ability to travel up to 70%, depending on project requirements. * Good knowledge and understanding of ICH GCP and worldwide applicable regulatory requirements * Good leadership, planning, project management skills, verbal communication skills, and written communication skills. * Knowledge and experience with MS Office suite (at a minimum Word, PowerPoint and Excel). If you have the experience required and want to join an energetic, creative, and collaborative team, please apply directly to our website at https://biorasi.com or email us at careers@biorasi.com. Biorasi is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. Biorasi is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

דרישות המשרה

. * Good knowledge and understanding of ICH GCP and worldwide applicable regulatory requirements * Good leadership, planning, project management skills, verbal communication skills, and written communication skills. * Knowledge and experience with MS Office suite (at a minimum Word, PowerPoint and Excel). If you have the experience required and want to join an energetic, creative, and collaborativ

NVIDIA is a world leader in Artificial Intelligence, High-Performance Computing, and Visualization. Our invention, the GPU, has transformed modern computing and is at the heart of our products and services. We set the standard in groundbreaking technology, making NVIDIA one of the technology industry’s most desirable employers. We are seeking a talented and passionate DevOps Engineer to join our team. If you excel at creative problem-solving, thrive in a fast-paced environment, and are eager to collaborate with distributed teams, we want to hear from you! What You’ll Be Doing * Design, build, and maintain robust HPC and cloud infrastructure utilizing state-of-the-art technologies and cutting-edge hardware. * Automate the deployment, configuration, and management of network and compute resources, including bare metal servers, network switches, and VMs. * Develop and streamline CI/CD pipelines to enable continuous integration and delivery for our R&D engineering teams. * Optimize infrastructure for availability, performance, observability, security, scalability, and cost-efficiency. * Collaborate closely with software development teams to integrate automated testing and quality assurance into deployment workflows. * Troubleshoot and resolve issues spanning infrastructure, networking, hardware, and software environments. * Stay current with industry trends and incorporate best practices in DevOps and infrastructure management. What We Need To See * Bachelor’s or Master’s degree in Computer Science, Data Science, Engineering, or a related field. * 2+ years of experience building and maintaining DevOps processes, with a strong focus on automation and reliability. * Solid experience with major Linux distributions (Ubuntu, RedHat). * Proficient scripting skills in Bash, Python, and Groovy. * Understanding of Linux virtualization technologies (QEMU/KVM, Docker) and orchestrators like Kubernetes. * Hands-on experience with configuration management tools (e.g., Ansible). * Knowledge in on-premises networking and compute infrastructure. * Familiarity with CI/CD tools such as Jenkins, GitHub/GitLab, Kubernetes, and GitHub Actions. * Excellent written and verbal communication skills in English. Ways To Stand Out From The Crowd * Experience working in agile DevOps teams and complex technical environments. * Proven ability to achieve or exceed security, reliability, scalability, and availability goals. * In-depth understanding of modern cloud and infrastructure architectures. * Passion for staying at the forefront of emerging technologies and best practices Join us and work on technologies that are transforming entire industries. We offer an innovative and inclusive environment where your contributions matter, and your ideas shape the future. JR2002146

דרישות המשרה

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שתף משרה זו Production Project Manager זיהוי דרישה: 4915 מיקום גאוגרפי: מרכז חברה: ElbitSystems עיר: חולון לאתר החברה בחולון דרוש.ה מנהל.ת פרויקט בייצור למרכז טכנולוגי מוביל בתחום מערכות הלוחמה האלקטרונית, המבצע מחקר, פיתוח וייצור מרכיבי ה RF והמיקרוגל במסגרת התפקיד: אחריות מקצה לקצה על תהליך תכנון הייצור בסביבה פרויקטלית סנכרון כל המחלקות הרלוונטיות לעמידה ביעדים: תפ”י, קווי הרכבות, בחינה, תחזוקה, הנדסת ייצור, אבטחת איכות הובלת דיון אספקות שבועי- בקרה על תכנית העבודה, זיהוי הזדמנויות וסיכונים התאמת תכנית העבודה ומתן פתרונות אופטימליים לשינויים בסביבת ייצור מורכבת ודינאמית שיפור תשתיות מידע ובניית דוחות וכלי תכנון מתקדמים הגדרת KPI, ניתוח נתונים והפקת דוחות דרישות: מהנדס.ת תעשייה וניהול ניסיון משמעותי בניהול פרויקטים בייצור או תפ”י בחברה גלובלית תקשורת בין אישית ויכולת מתן שירות מקצועי לכל הממשקים גישה פרואקטיבית ולקיחת אחריות ניסיון בסביבת עבודה MRP/ERP שליטה ב excel ברמה גבוהה אנגלית ברמה טובה * המשרה מיועדת לגברים ונשים כאחד * פניות מתאימות בלבד יענו

דרישות המשרה

מהנדס.ת תעשייה וניהול ניסיון משמעותי בניהול פרויקטים בייצור או תפ”י בחברה גלובלית תקשורת בין אישית ויכולת מתן שירות מקצועי לכל הממשקים גישה פרואקטיבית ולקיחת אחריות ניסיון בסביבת עבודה MRP/ERP שליטה ב excel ברמה גבוהה אנגלית ברמה טובה * המשרה מיועדת לגברים ונשים כאחד * פניות מתאימות בלבד יענו

About Us We, at AUI, are pioneering the next generation of conversational AI agents with Apollo-
1. Apollo-1 isn’t just another language model; it’s a breakthrough Neuro-Symbolic foundation model for controllable agents, designed from the ground up to finally solve the controllability problem in conversational AI. This unique approach enables capabilities that the standard transformer models lack, such as reliable, native tool use and unprecedented granular control over agent behavior in each interaction, including the ability to implement hard rules and continuously fine-tune performance based on real-world feedback. Apollo-1 is demonstrating state-of-the-art results in demanding domains like retail and travel. We believe this technology is the essential unlock for truly reliable and scalable conversational agents across consumer and enterprise applications, moving the entire field forward. We invented this approach, and we’re looking for passionate individuals to help us bring its power to the world. The Role: QA Engineer We’re seeking a detail-oriented QA Engineer to ensure the quality, stability, and reliability of our AI-driven products. You’ll be hands-on in testing Apollo’s applications, identifying issues early, and helping maintain the high standards that define our technology. What You’ll Do: * Design, write, and execute manual test cases across web and mobile applications * Support automated testing by creating or maintaining test scripts (where applicable) * Identify, document, and track bugs through to resolution * Perform regression, smoke, and end-to-end testing for new and existing features * Collaborate closely with developers and product managers to clarify requirements and improve product quality * Contribute to continuous improvement of QA processes and testing tools * Stay informed on best practices and emerging trends in software testing Who We’re Looking For: * A passionate QA professional with a strong eye for detail and a drive for excellence * A proactive problem-solver who thrives in fast-paced, innovative environments * A clear communicator who values collaboration and continuous improvement Requirements: * 3+ years of experience in manual software testing * Solid understanding of QA methodologies, tools, and processes * Experience in functional, regression, and end-to-end testing * Familiarity with Agile/Scrum development environments * Experience using bug tracking and test management tools (e.g. Jira, TestRail) * Strong analytical and documentation skills * Excellent communication skills in English * Ability to work effectively in remote and cross-functional teams * Knowledge of automation frameworks or scripting languages (a plus) * Exposure to performance or security testing (a plus) * Experience testing an AI/LLM based product If you’re excited about ensuring the quality of groundbreaking AI technology and contributing to the excellence of next-generation conversational agents, we’d love to hear from you.

דרישות המשרה

and improve product quality * Contribute to continuous improvement of QA processes and testing tools * Stay informed on best practices and emerging trends in software testing Who We’re Looking For: * A passionate QA professional with a strong eye for detail and a drive for excellence * A proactive problem-solver who thrives in fast-paced, innovative environments * A clear communicator who values c

Quality Engineer Location: BEN GURION AIRPORT Duration: On-Going contract Frequency: 40hrs per week Compensation: $60/hr. USD (ILS ₪212.916) Please submit your CV in English Preference for a US Citizen or dual-citizen. If not a US Citizen, ability to secure a DSP-5 Position Overview: Job Description: * Utilize quality science techniques to effect continuous performance improvement at assigned suppliers. * Reviews, analyzes, and reports on quality discrepancies related to process, assembly, manufacturing, mechanical, electrical, hydraulic, or electro-mechanical systems. * Ensure that performance and quality of products conform to established company and regulatory standards. * Use surveillance and auditing techniques to identify opportunities for process and product improvement. * Interfaces with manufacturing, engineering, customer, supplier, and procurement (as appropriate) to ensure requirements / expectations are satisfied. * Facilitate development of supplier recovery plans. * Monitor and evaluate supplier process for compliance to purchase order and engineering requirements. * Collaborate with supplier to investigate root cause and corrective actions when process or product deficiencies are detected. * Identify, plan, and facilitate cross-functional improvement activities. * Deploy variation management tools and techniques at select suppliers to mitigate risk. * Computer proficiency and proficiency with MS Office products. Additional Comments: * Travel is required and may extend beyond the local area. * Initial supplier assignments may change to meet customer requirements. * Work hours are not fixed or guaranteed and may extend beyond 40 hours per week to meet customer requirements. * Aerospace supplier experience is preferred and may be used as the primary selection criteria among equally qualified candidates. Skills Requirement: * Have performed Quality System Audits, AS9102 First Article Reviews. * Experience with large complex airframe assemblies desired. * Production (or Manufacturing) Quality Assurance/Control in Aerospace industry (or similar). * Ability to interpret blueprints and specifications. * Collaborate with production personnel and stakeholders. * Identify and drive root cause and corrective actions. * Execute on deliveries. * Attention to Detail. * Strong communication skills. * In process and Final Inspection. Requirements: * 5+ Years experience in Aerospace Quality engineering * 5+ years’ experience in FAI and AS9102 “We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, age, political affiliation, marital status, disability status, protected veteran status, or any other characteristic protected by law. Verify, Inc. will not tolerate discrimination or harassment based on any of these characteristics.”

דרישות המשרה

/ expectations are satisfied. * Facilitate development of supplier recovery plans. * Monitor and evaluate supplier process for compliance to purchase order and engineering requirements. * Collaborate with supplier to investigate root cause and corrective actions when process or product deficiencies are detected. * Identify, plan, and facilitate cross-functional improvement activities. * Deploy var

About Ashtrom Renewable Energy: Ashtrom Renewable Energy operates as an independent power producer (IPP) and specializes in developing, financing, constructing, and operating large-scale renewable energy projects. We are looking for an experienced Project Development Manager to lead strategic and large-scale projects in the energy sector, combining economic, financial, engineering, and operational aspects. Location: Israel Full-time position Willingness to travel to the U.S. Key Responsibilities: * End-to-end management of projects – from feasibility through development to full maturity * Overseeing the entire project development process * Performing comprehensive project analysis, including planning, contractual, financial, and budgeting aspects * Coordinating between technical, financial, regulatory teams and external suppliers * Managing project risks and leading quality assurance and control processes * Monitoring project timelines and ensuring alignment with business goals and milestones * Preparing and presenting regular reports to management in Israel and abroad Requirements: * Minimum 5 years of experience in project management within the energy sector – required * Relevant academic degree in Law, Engineering, Economics, Industrial Engineering & Management, or a related field – required * Proven experience in managing complex, global projects – required * Background in energy companies – Solar, Wind, Electricity, or other Renewable Energy sectors – required * Excellent English – written and verbal communication * Willingness to travel to the United States

דרישות המשרה

* End-to-end management of projects – from feasibility through development to full maturity * Overseeing the entire project development process * Performing comprehensive project analysis, including planning, contractual, financial, and budgeting aspects * Coordinating between technical, financial, regulatory teams and external suppliers * Managing project risks and leading quality assurance and c

About The Position About AllCloud AllCloud is a global professional services company providing organizations with the tools for cloud enablement and transformation. As an AWS Premier Consulting Partner and audited MSP, a Salesforce Platinum Partner and Snowflake Premier Partner, AllCloud helps clients connect their front office and back office by building a new operating model that allows them to harness the benefits of cloud technology and data and analytics. Job Summary AllCloud is looking for an experienced Salesforce Consultant to join our team of experts. The candidate will be responsible for understanding our customers’ business & implementation requirements and for migrating customers to Salesforce to support those requirements. The Salesforce Consultant will be responsible for performing business analysis in order to support the following departments
– Sales, Customer Service, Partner Management, and Operations teams. Summary Of Key Responsibilities * Analyze customer business requirements and define future needs based on Salesforce best practices * Configure the Salesforce application based on the customer requirements * Implementation and support activities for projects * Allocate tasks including project timelines * Deliver projects, using the most appropriate Salesforce tools and techniques * Apply best practices to build the Salesforce applications * Work with internal and external interfaces * Implement business functionality * Research Salesforce capabilities as needed to suit business requirements * Perform Quality Assurance of customer projects Requirements * 2 years of experience in designing and implementing the Salesforce platform * Experience in understanding the customer, writing full characterization documents * High personal level, high level of service and technical capabilities * Understanding of design patterns * Problem solving and multitasking skills * Creative and flexible attitude * Excellent oral and written communication skills * Team player Advantages * Graduate of Industrial Engineering * Salesforce Admin certification AllCloud is an Equal Opportunity Employer and considers applicants for employment without regard to race, color, religion, sex, orientation, national origin, age, disability, genetics or any other basis forbidden under federal, provincial, or local law.

דרישות המשרה

and for migrating customers to Salesforce to support those requirements. The Salesforce Consultant will be responsible for performing business analysis in order to support the following departments
– Sales, Customer Service, Partner Management, and Operations teams. Summary Of Key Responsibilities * Analyze customer business requirements and define future needs based on Salesforce best practices *

Job Description Job Purpose Monitoring, validation and analyses of cross asset derivatives and listed markets. On boarding OTC and listed market data pricing into ICE Data Services systems and downstream products. Responsibilities * Monitor and validation of cross asset raw and derived market data using in-house analytical tools. * Providing customers with accurate, real time and historical, response to their data related queries. * Work closely with internal departments such as operations and support. * Data quality checks and uploads * Analyze cross asset market data using Excel, SQL and in house tools. * Troubleshoot data inconsistences. * Monitor global financial news. * Maintenance of documentation, identify areas of improvement, and carry out quality assurance on team documentation. Knowledge And Experience * BA/BSc in Business, Finance, Statistics, Economics or Financial Engineering. * Proficient in Excel * SQL- an advantage * Interest and familiarity with financial markets * Team player, Independent and a fast learner * Ability to work under pressure. * Organized and detail oriented.

דרישות המשרה

* Monitor and validation of cross asset raw and derived market data using in-house analytical tools. * Providing customers with accurate, real time and historical, response to their data related queries. * Work closely with internal departments such as operations and support. * Data quality checks and uploads * Analyze cross asset market data using Excel, SQL and in house tools. * Troubleshoot dat

* Warehouse Manager, Priority ERP – Must Qualifications * Priority ERP – Must * Good command of English
– Must. * Experience from a Hi Tech Company
– Must * Bachelor’s degree in supply chain management, business administration, or a related field. * Minimum of 3 years of experience in warehouse or supply chain operations. * Strong communication and interpersonal skills. * Ability to analyze and interpret data for informed decision-making. * Excellent problem-solving skills and attention to detail. * Familiarity with radar systems operation and engineering degrees is a plus. Responsibilities * Oversee inventory levels to ensure sufficient stock is available to meet customer needs. * Organize inventory and maintain precise tracking records. * Supervise all warehouse logs and conduct regular inventory counts. * Support the operations team with order fulfillment and quality assurance processes. * Monitor shipments and coordinate delivery timelines. * Manage shipping processes and overall warehouse activities. * Review outstanding and completed sales orders and invoices. * Generate and organize sales orders, invoices, productivity reports, packing lists, and other essential documents. * Collaborate closely with the customer service team to address and resolve issues. * Work with suppliers, vendors, and distributors to obtain raw materials and finished products. * Follow all company policies and procedures.

דרישות המשרה

* Priority ERP – Must * Good command of English
– Must. * Experience from a Hi Tech Company
– Must * Bachelor’s degree in supply chain management, business administration, or a related field. * Minimum of 3 years of experience in warehouse or supply chain operations. * Strong communication and interpersonal skills. * Ability to analyze and interpret data for informed decision-making. * Excellent p

ובד/ת מעבדה בכיר/ה (ראש צוות) מחפש/ת את הצעד הבא בקריירה שלך? לחברת נירלט דרוש/ה ראש/ת צוות למעבדת האיכות, שבהמשך יהווה מנהל/ת מעבדת הפיתוח קטן ותהליכים מקצועיים. מה כוללת העבודה? הובלה והדרכה של צוות מעבדה מקצועי ביצוע ובקרה של בדיקות איכות על מוצרים וחומרי גלם שותפות פעילה בתהליכי בקרת איכות ושיפור מתמיד בקווי הייצור תמיכה במחלקות הייצור, אבטחת האיכות והשיווק באמצעות בדיקות, ניסויים וייצור דוגמאות טיפול בתקלות ובאתגרי איכות, תוך מתן פתרונות מקצועיים ומהירים עבודה עם ציוד ומכשור אנליטי מתקדם בסביבה טכנולוגית מגוונת דרישות ניסיון בעבודה במעבדה תעשייתית – חובה ניסיון בהובלת צוות / ריכוז פעילות צוותית – חובה שליטה בציוד ומכשור אנליטי יכולת עבודה בסביבה דינמית עם ריבוי משימות תודעת שירות גבוהה ויחסי אנוש מצוינים אנגלית ברמה טובה (קריאה וכתיבה של דוחות מקצועיים) תואר ראשון בכימיה / פיזיקה / תעשייה וניהול – יתרון משמעותי * נכונות לשעות נוספות במידת הצורך

דרישות המשרה

ניסיון בעבודה במעבדה תעשייתית – חובה ניסיון בהובלת צוות / ריכוז פעילות צוותית – חובה שליטה בציוד ומכשור אנליטי יכולת עבודה בסביבה דינמית עם ריבוי משימות תודעת שירות גבוהה ויחסי אנוש מצוינים אנגלית ברמה טובה (קריאה וכתיבה של דוחות מקצועיים) תואר ראשון בכימיה / פיזיקה / תעשייה וניהול – יתרון משמעותי * נכונות לשעות נוספות במידת הצורך

פינובסט, פלטפורמת ייעוץ ההשקעות הדיגיטלית המובילה בישראל, המוטמעת בגופים פיננסיים ומשרתת עשרות רבות של אלפי לקוחות קצה, מחפשת בודק/ת QA יסודי/ת, סקרן/ית ובעל/ת אחריות גבוהה, שיצטרף לצוות שלנו בתל-אביב. מה תעשי/ה אצלנו? * השגחה על מערכת מסחר אוטומטית. * בדיקות תוכנה מקצה לקצה – לווב ולמובייל. * עבודה בצמוד לצוות הפיתוח והמוצר לשמירה על אמינות, ביצועים וחוויית משתמש מושלמת. * אחריות על זיהוי תקלות, תיעודן ומעקב אחרי תיקונים. מה אנחנו מחפשים? * אחריות, סדר ודיוק בפרטים הקטנים. * יכולת למידה עצמית וחשיבה אנליטית. * הבנה בסיסית במערכות מסחר או עניין בעולם הפיננסי
– יתרון משמעותי. * זמינות לעבודה במשרדי החברה בתל אביב, בימים שני עד שישי(עד הצהריים). בונוס (רציני): אם את/ה גם אוהב/ת לבשל – זה יתרון אמיתי! אצלנו מבשלים גורמה (וביחד ).

דרישות המשרה

לא צויין

The Meta Technical Program Management community is pioneering technologies to bring people (and businesses) closer together at a global scale. Technical Program Managers work at the cross-section between technical execution and business strategy and are expected to partner closely with Engineering, Product, and other cross functional teams. Being a TPM at Meta means driving impact by delivering measurable results across a wide range of areas. You’ll be responsible for defining and guiding high-level goals and roadmaps, monitoring and communicating progress, and defining requirements for new products and features. It also means having a technical background, understanding system architecture, and the experience to effectively collaborate across functions and organizations to deliver impact.You will be leading technical strategy and execution on the company-wide platforms and services that are used across Facebook, WhatsApp, Instagram, Messenger, and Reality Labs. Teams span across Ads, Business Integrity, Monetization, Commerce, Business Messaging, Privacy, Social Impact, Central Integrity, Growth, Central Metrics, Internationalization, Platforms for Family of Apps, Groups, Search, Foundation, Infrastructure, the Metaverse, and other areas. This posting represents different full-time roles across the company. Technical Program Manager Responsibilities: * Drive complex programs fully autonomously, creating structures that drive efficient execution * Manage and own cross-functional products and programs execution in a matrix organization * Drive and influence technical and product strategy, proactively identify risks and develop mitigation strategies, align on priorities, and set direction for a broadly cross-functional area * Help define the roadmap and long-term strategy of the teams that you are working with * Design measurements to track impact and drive internal process improvements * Define goals and milestones for your programs with clear technical strategy” * Collaboratively define the strategy for building Meta-scale, state-of-the-art, global products * Develop and manage end-to-end project plans to ensure on-time delivery, provide day-to-day coordination, and quality assurance for tasks * Move fast in a flat organization by working in concert with technical program managers, product managers and engineers across Meta to establish a shared vision for improving execution and building solutions * Ongoing communication of planning, project status, issues and risks in a timely fashion to stakeholders * Help drive product decisions to align with higher company initiative * Establish shared goals with product teams across the company to build alignment across multiple cross-functional teams and to build and scale products for Meta Minimum Qualifications: * B.S. in Computer Science or a related technical discipline, or equivalent experience * Experience driving and delivering complex tech programs or products from inception to delivery * Experience defining strategic direction and identifying new opportunities for impact amongst products, platforms and programs * Knowledge of user needs, gathering requirements, and defining scope * Experience operating across multiple teams and functions, demonstrated critical thinking, and thought leadership * Communication experience at executive level and experience influencing leadership and technical management teams to develop systems, solutions, and products * Organizational, coordination and multi-tasking experience * Analytical and problem-solving experience with large-scale systems * Experience establishing work relationships across multi-disciplinary teams and multiple partners in different time zones * Experience working with product teams to build and deliver end-to-end customer focused products with technical knowledge of the underlying platforms and technologies About Meta: Meta builds technologies that help people connect, find communities, and grow businesses. When Facebook launched in 2004, it changed the way people connect. Apps like Messenger, Instagram and WhatsApp further empowered billions around the world. Now, Meta is moving beyond 2D screens toward immersive experiences like augmented and virtual reality to help build the next evolution in social technology. People who choose to build their careers by building with us at Meta help shape a future that will take us beyond what digital connection makes possible today—beyond the constraints of screens, the limits of distance, and even the rules of physics. Individual compensation is determined by skills, qualifications, experience, and location. Compensation details listed in this posting reflect the base hourly rate, monthly rate, or annual salary only, and do not include bonus, equity or sales incentives, if applicable. In addition to base compensation, Meta offers benefits. Learn more about benefits at Meta.

דרישות המשרה

for new products and features. It also means having a technical background, understanding system architecture, and the experience to effectively collaborate across functions and organizations to deliver impact.You will be leading technical strategy and execution on the company-wide platforms and services that are used across Facebook, WhatsApp, Instagram, Messenger, and Reality Labs. Teams span ac

The QA/RA Project Manager is responsible for Regulatory Affairs & Quality Assurance. Job Description:
• Lead compiling and preparing materials for submission to regulatory authorities. Lead Quality Management System (QMS) and medical device development and production, according to the project’s scope and needs.
• Coordinate and document internal processes, such as employees training and qualifications, internal audits, Corrective and Preventive Actions (CAPAs) and Management Reviews.
• Lead and/or support the R&D Team in design control activities and related processes such as Design History File (DHF) maintenance, Verification and Validation (V&V) testing, risk management and change control.
• Evaluate, approve, and monitor the customer’s suppliers / clients and sub-contractors. Required Background:
• Previous experience in the QA and/or RA fields in the medical device industry including SW.
• Relevant University/Professional background (life science, biomedical, biochemistry, etc.) Required Skills:
• Passionate about life sciences, technology, and innovation.
• Strong communication and interpersonal skills.
• Highly motivated, committed, and responsible.
• Ability to work independently, and as part of a team.
• Willing to learn.
• Good verbal and written English skills.

דרישות המשרה

, internal audits, Corrective and Preventive Actions (CAPAs) and Management Reviews.
• Lead and/or support the R&D Team in design control activities and related processes such as Design History File (DHF) maintenance, Verification and Validation (V&V) testing, risk management and change control.
• Evaluate, approve, and monitor the customer’s suppliers / clients and sub-contractors. Required Backg

About Nanit: Welcome to Nanit, the high-growth baby tech company that is changing the way parents view their babies’ wellness through the world’s most advanced baby monitor and parenting products. In 2016, the Nanit baby monitor revolutionized the industry with computer-vision and machine-learning capabilities that helped parents understand their baby’s sleep patterns and allowed them to achieve better sleep quality. Now, the company has become the leader in the connected parenting space, with an incredible customer base of highly engaged parents who look to Nanit as a source of information and expertise on their parenting journey. What You’ll Do: * Review quality specifications and technical design documents to provide timely and meaningful feedback * Create detailed, comprehensive, and well-structured test plans and test cases * Estimating, prioritizing, planning, and coordinating quality testing activity * Identify, record, document thoroughly, and track bugs * Work closely with product managers, project managers, developers, and customer servic Who You Are: * 2+ years of quality assurance experience. * Experience in mobile applications testing on both iOS and Android platforms * Understanding of complex products (client-side and backend side) * Debugging skills, ability to read logs, and understanding the root cause of issues * Great personal skills, a team player with a ‘can-do’ approach * High attention to detail, strong analytical and problem-solving skills * Multitasking, dealing with a high rate of context switching * Fully comfortable working in English, both in writing and speaking Nice to have: * Automation experience
– Advantage * Python knowledge
– Advantage * Firmware Testing experience
– Advantage * Experience working in an Agile/Scrum development process
– Advantage * Experience with multidisciplinary products, Mobile, Web, HW, AI, and Server- advantage Why Nanit? * Nanit products can actually change lives. We’re an integral part of the lives of new parents, making an exciting but stressful time a little more manageable. * We are international and believe our diversity makes our culture, products, and brand even better. * We invest in our people. We consider each employee a long-term investment and we see value in continuously helping them to advance in their lives and careers * Nanit is a fun, collaborative group of hard workers! We believe in an appropriate work-life balance and offer a flexible, open environment. * We are at the forefront of innovation, creating products and services that have never been seen before. We are proud to be an equal-opportunity employer. We provide employment opportunities without regard to age, race, color, ancestry, national origin, religion, disability, sex, gender identity or expression, sexual orientation, veteran status, or any other protected class.

דרישות המשרה

לא צויין

^^משרה זו נלקחה מ INDEED^^
למפעל אסם יקנעם דרוש/ה אחראי/ת איכות ומנהל/ת תחום בקרת איכות תחומי אחריות ניהול ישיר של צוות מבקרי האיכות במפעל ניהול פעילות פאנל סנסורי יומי קידום וחיזוק תרבות האיכות ברצפת הייצור חניכה ושיפור הידע בנושא דרישות האיכות בקרב עובדי המפעל ברצפת הייצור. אחריות על מספר קווי יצור בהיבטי איכות יוזמה של פעולות פרואקטיביות לשיפור קיום נהלי האיכות לצמצום אירועי אי איכות. הובלת ניתוח ותחקירי שורש לתלונות חריגות / גופים זרים השתתפות כחבר צוות HACCP ו
• preHACCP הובלה של תחומי איכות נוספים ברמה מפעלית בהתאם לדרישות נסטלה העולמית השתתפות בפעילויות ה TPM במפעל דרישות התפקיד רקע אקדמי בתחום המזון / ביוטכנולוגיה/מדעי החיים (מהנדס.ת מזון / ביוטכנולוגיה / מדעי המזון)
• חובה. ניסיון קודם של שנתיים ומעלה בהבטחת איכות במפעל מזון מוביל
• חובה. ניסיון ניהולי
• יתרון הכרות עם דרישות האיכות לפי ISO 9001 (מבדקים פנימיים, סקר הנהלה, שיפור מתמיד וכו’)
• יתרון. יכולת הנעת תהליכים ויחסי אנוש טובים אנגלית ברמה גבוהה נדרשת הגעה עצמאית

דרישות המשרה

האיכות בקרב עובדי המפעל ברצפת הייצור. אחריות על מספר קווי יצור בהיבטי איכות יוזמה של פעולות פרואקטיביות לשיפור קיום נהלי האיכות לצמצום אירועי אי איכות. הובלת ניתוח ותחקירי שורש לתלונות חריגות / גופים זרים השתתפות כחבר צוות HACCP ו
• preHACCP הובלה של תחומי איכות נוספים ברמה מפעלית בהתאם לדרישות נסטלה העולמית השתתפות בפעילויות ה TPM במפעל דרישות התפקיד רקע אקדמי בתחום המזון / ביוטכנולוגיה/מדעי החיי

דרושים עובדים לבקרת איכות לקיסריה. אפשר ללא ניסיון! הכשרה על חשבון החברה. עבודה במשמרות, מ7 עד 19, או מ19 בערב עד 7 בבוקר. שכר 14000!

דרישות המשרה

ניסיון

מתויג כ: ללא ניסיון

**דרוש/ה לבורנט/ית למעבדת בקרת איכות | אזור כפר סבא** חברה תעשייתית מובילה באיזור כפר סבא מחפשת לבורנט/ית למעבדת בקרת איכות לתפקיד מגוון, יציב ובעל משמעות בלב תהליכי הייצור והחדשנות של החברה. התפקיד כולל ביצוע בדיקות איכות לחומרי גלם ולמוצרים, תיעוד וכתיבת דוחות, עבודה צמודה עם צוותי הייצור והלוגיסטיקה, ודאגה לסדר, ניקיון ותקינות המעבדה. דרישות התפקיד : * תעודת הנדסאי/ת או טכנאי/ת בתחומים רלוונטיים (כימיה, חומרים, ביוטכנולוגיה או תחום דומה) חובה * ניסיון קודם במעבדה תעשייתית יתרון גדול * שליטה בתוכנות Office ובמערכות ERP / LIMS יתרון * נכונות לעבודה במשמרות (בוקר / ערב) * נכונות לביצוע משימות הכוללות מאמץ פיזי מתון (כגון נשיאת דגימות, שקילת חומרים, הזזת ציוד מעבדה) מחפש/ת עבודה משמעותית בסביבה מקצועית, עם יציבות, תנאים טובים ואווירה משפחתית? נשמח להכיר אותך. שליחת קו”ח: וואטסאפ: 054 2443473

דרישות המשרה

דרישות התפקיד : * תעודת הנדסאי/ת או טכנאי/ת בתחומים רלוונטיים (כימיה, חומרים, ביוטכנולוגיה או תחום דומה) חובה * ניסיון קודם במעבדה תעשייתית יתרון גדול * שליטה בתוכנות Office ובמערכות ERP / LIMS יתרון * נכונות לעבודה במשמרות (בוקר / ערב) * נכונות לביצוע משימות הכוללות מאמץ פיזי מתון (כגון נשיאת דגימות, שקילת חומרים, הזזת ציוד מעבדה) מחפש/ת עבודה משמ

מתויג כ: הנדסאי, טכנאי

עבודה מול מכונת הרכבה, בקרת איכות ואריזה. 3 משמרות | עבודה פיזית (עמידה/ ישיבה) | נכונות לעבודה בסופ”ש| ארוחות חמות בכל יום הסעות מאזורי מגורים נבחרים!! לפרטים: 054 7044949

דרישות המשרה

לא צויין

דרוש/ה טכנולוג/ית מזון מנוסה ↙ לתפקיד מנהל אבטחת האיכות של חברת מזון מובילה בירושלים. הגדרת התפקיד ותחומי אחריות: נציגה הבכיר של ההנהלה לכל נושא איכות המזון, בטיחות מוצר ובטיחות המזון. ניהול מערכת האיכות בחברה ISO ,HACCP , GMP וניהול הסמכות. אחריות על קבלת כלל הרישיונות לחברה, רישיון יצרן, רישיון עסק וכדו׳. אחריות לקשר עם גורמי חוץ, כגון: משרד הבריאות, משרד החקלאות, משרד איכות הסביבה, מכון התקנים, וטרינרים עירוניים, רשויות מקומיות, יועצים ומעבדות. בקרת איכות שוטפת בתחום האיכות והבטיחות במזון במטבחי ואתרי החברה. בקרת איכות אישור והסמכת ספקים. אחריות על הנחיות בטיחות מזון, הדרכות מקצועיות והטמעת תהליכים בתחומי האיכות ובטיחות המזון למנהלי ועובדי החברה. פיתוח ועדכון מדדי בטיחות מזון ואיכות מזון והצגתם להנהלה באופן שוטף. מיפוי ועדכון של תרשימי הזרימה במפעלים וביצוע בקרות שוטפות. דרישות התפקיד: ניסיון מוכח כטכנולוג/ית מזון במפעלי ייצור בתחום המזון / המטבח התעשייתי / מוסדי. שליטה בתקני ISO, HACCP, GMP ונהלי משרד הבריאות. ידע וניסיון בעבודה מול גורמי פיקוח, רישוי ורגולציה. יכולת כתיבת מפרטי ייצור והטמעת תהליכי עבודה במערך ייצור מורכב. הבנה טכנולוגית מעמיקה בחומרי גלם, תהליכי בישול, הקפאה, אחסון ואריזה. היכרות עם מערכות ERP (Priority) יתרון משמעותי. גישה מערכתית, ירידה לפרטים, אחריות אישית ויכולת עבודה תחת לחץ. תואר ראשון לפחות במדעי המזון / הנדסת מזון חובה. משרה מלאה, ימי שישי לפי צורך. * משרה מס׳ #758829 מיועדת לגברים ונשים כאחד קישור לשיתוף ולהגשת מועמדות ↙

דרישות המשרה

דרישות התפקיד: ניסיון מוכח כטכנולוג/ית מזון במפעלי ייצור בתחום המזון / המטבח התעשייתי / מוסדי

מתויג כ: תואר ראשון

לכפרית תעשיות בכפר עזה דרושים/ות עובדי **בקרת איכות בייצור, אריזה וייצור** לעבודה במשמרות בסיס **39 ₪ לשעה** | ארוחות | הסעות לפרטים: 054 2244331

דרישות המשרה

דרושים/ות עובדי **בקרת איכות בייצור, אריזה וייצור** לעבודה במשמרות בסיס **39 ₪ לשעה** | ארוחות | הסעות לפרטים: 054 2244331

דרוש/ה ממונה בטיחות, אבטחת איכות ואיכות הסביבה לתעשייה כבדה באשדוד מיקום: מפעל מוביל באזור אשדוד תיאור התפקיד: אחריות כוללת על מערכות הבטיחות, האיכות ואיכות הסביבה במפעל בניית תוכנית בטיחות שנתית ויישומה בשטח פיקוח ובקרה על נהלי בטיחות ואיכות עבודה דיווחים תקופתיים למשרד להגנת הסביבה ולגורמים רגולטוריים ביצוע מבדקים פנימיים וחיצוניים ויישום תוכניות דרישות התפקיד הסמכה רשמית כממונה בטיחות בעבודה חובה תואר ראשון כימיה / הנדסה/ מדעי הסביבה חובה שליטה בכל ישומי המחשב שכר 25.000 ש”ח כולל רכב חברה צמוד להגשת מועמדות מיטל

דרישות המשרה

דרישות התפקיד הסמכה רשמית כממונה בטיחות בעבודה חובה תואר ראשון כימיה / הנדסה/ מדעי הסביבה חובה שליטה בכל ישומי המחשב שכר 25.000 ש”ח כולל רכב חברה צמוד להגשת מועמדות מיטל

מתויג כ: תואר ראשון

^^משרה זו נלקחה מ Career^^Description לאתר של דלתא גליל בכרמיאל דרוש.ה טכנאי.ת מעבדה אבטחת איכות
• החלפה לחל”ד מטרת התפקיד: ביצוע בדיקות מעבדה מקצועיות על פי דרישות לקוח, תקנים בינלאומיים (AATCC, ASTM, ISO) ונהלי החברה, במטרה לוודא את עמידות ואיכות מוצרי הטקסטיל (בדים, גרביים, פריטי סימלס ומוצרים מוגמרים). תחומי אחריות עיקריים: ביצוע בדיקות פיזיקליות ובדיקות יציבות צבע לפי פרוטוקולים מוגדרים בדיקת מגוון רחב של מוצרים טקסטיליים בהתאם לדרישות פנימיות וחיצוניות הכנת דוגמאות לבדיקה, כולל חיתוך, שקילה והכנת תמיסות כימיות הפעלת ציוד מעבדה בהתאם לנהלי בדיקה ותקנים ניתוח תוצאות הבדיקות, הסקת מסקנות והפקת דוחות מקצועיים כיולים יומיים של ציוד (לדוגמה: מד pH), ניקיון ותחזוקה שוטפת של אזור העבודה עבודה שוטפת מול צוותים עסקיים, מחלקות פיתוח, רכש ומעצבות לצורך קבלת דוגמאות ומעקב הגשת דוחות לאישור מנהלת המעבדה ומעקב אחר שליחתם לגורמים הרלוונטיים Requirements ידע בסיסי בכימיה
• חובה הנדסאי/ת כימיה או אבטחת איכות או תחום משיק אחר ניסיון של שנה במעבדת בדיקות או בתפקיד דומה
• יתרון, עדיפות לניסיון בתחום הטקסטיל שליטה טובה בעברית ובאנגלית, כולל יכולת קריאה וכתיבת דוחות ואימיילים באנגלית שליטה ביישומי Office: Word, Excel, Windows יחסי אנוש מעולים, יכולת עבודה בצוות וגם באופן עצמאי יכולת עבודה תחת עומס וריבוי משימות נכונות ללמוד תהליכים ובדיקות חדשות באופן שוטף בדלתא אנחנו מאמינים בשוויון הזדמנויות והמשרה פונה לכל המגדרים. כמו כן, אם אתם זקוקים להתאמות בתהליך הגיוס
• נשמח לסייע

דרישות המשרה

לקוח, תקנים בינלאומיים (AATCC, ASTM, ISO) ונהלי החברה, במטרה לוודא את עמידות ואיכות מוצרי הטקסטיל (בדים, גרביים, פריטי סימלס ומוצרים מוגמרים). תחומי אחריות עיקריים: ביצוע בדיקות פיזיקליות ובדיקות יציבות צבע לפי פרוטוקולים מוגדרים בדיקת מגוון רחב של מוצרים טקסטיליים בהתאם לדרישות פנימיות וחיצוניות הכנת דוגמאות לבדיקה, כולל חיתוך, שקילה והכנת תמיסות כימיות הפעלת ציוד מעבדה בהתאם לנהלי בדיקה ותקנים נ

^^משרה זו נלקחה מ Career^^At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function: Quality Job Sub Function: R&D/Scientific Quality Job Category: Professional All Job Posting Locations: Yokneam, Haifa District, Israel Job Description: About Cardiovascular Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech We are searching for the best talent for Standards Quality Lead to be in Yokneam. This role is responsible for driving the implementation and maintenance of Quality & Compliance processes related to standards and regulations within New Product Development (NPD). The position ensures alignment with internal Johnson & Johnson policies, global regulatory requirements, and industry standards. It serves as a key interface between cross
• functional teams to ensure product compliance, reliability, and quality throughout the development lifecycle. Key Responsibilities: Compliance with Standards & Regulations Lead the deployment of Quality & Compliance processes for new products, ensuring adherence to both internal J&J standards and external regulatory requirements. Provide technical support to hardware teams for safety, electromagnetic compatibility (EMC), and environmental testing at certified laboratories. Actively participate in the Global Standards Council quarterly meetings; review and analyze reports to identify relevant standards for inclusion in the Standards and Regulations Management Meetings. Organize and lead Standards and Regulations Management Meetings, ensuring effective tracking, assessment, and implementation of applicable standards. Conduct gap assessments against external and internal standards; initiate and follow up on corrective actions with Subject Matter Experts (SMEs). Notify SMEs of new or revised standards and coordinate related compliance activities. Drive completion of standards compliance activities in collaboration with SMEs and project teams. Maintain and update the Standards and Regulations Management SOP and the master list of applicable standards. Act as a Subject Matter Expert (SME) during internal and external audits, CAPA investigations, and updates to technical documentation. Quality Integration in NPD Provide quality input to NPD Quality & Compliance deliverables, including Quality Plans and Critical to Quality (CTQ) parameters. Develop and implement methodologies to assess and improve product reliability and quality during development. Collaborate with cross
• functional teams including Quality Assurance, Regulatory Affairs, R&D, Clinical, and Medical Safety Office (MSO) to ensure comprehensive compliance and product excellence. Qualifications: Education: Required: Bachelor’s degree (BA) Preferred: BSc in Engineering, Mechanical Engineering, Quality, Statistics, or a related technical field Experience: Proven experience as a Quality Engineer, ideally within the active medical device industry Strong understanding of regulatory standards (e.g., ISO, IEC, FDA, EU MDR) and product development processes Experience working with cross
• functional teams in a matrixed organization Skills & Competencies: Deep knowledge of standards management and regulatory compliance Strong analytical and problem
• solving skills Excellent communication and stakeholder management abilities Ability to lead meetings and drive cross
• functional alignment Detail
• oriented with strong organizational skills #LI
• LM5 At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. Do Not Sell or Share My Personal Information Limit the Use of My Personal Information

דרישות המשרה

, and industry standards. It serves as a key interface between cross
• functional teams to ensure product compliance, reliability, and quality throughout the development lifecycle. Key Responsibilities: Compliance with Standards & Regulations Lead the deployment of Quality & Compliance processes for new products, ensuring adherence to both internal J&J standards and external regulatory requirement

^^משרה זו נלקחה מ Career^^Description אנחנו ב
• KPMG ISRAEL, פירמה גלובלית מהגדולות בעולם, מתמחים בשירותי ביקורת וייעוץ עסקי ומלווים את החברות המובילות במשק, הצמיחה שלנו מונעת ע”י תוצאות אמתיות עבור הלקוחות שלנו. האנשים שלנו הם שהופכים את הפירמה למקום הטוב ביותר לעבוד בו, אנו מעודדים פיתוח אישי ומקצועי, סביבה עבודה ייחודית, מתגמלת, חדשנות ומצוינות. זה המקום להזניק את הקריירה שלכם
• ללמוד, להתפתח, להיות משמעותיים ולהשפיע! גאים לשתף שבזכות האנשים שלנו נבחרנו בפעם השנייה ברציפות “למעסיק הטוב ביותר” עפ”י עיתון גלובס KPMG מחפשת יועצ.ת בכיר.ה ומנוסה בתחום כתיבת המכרזים הטכנולוגיים התפקיד כולל אחריות מלאה על תהליך כתיבת המכרז
• החל משלב האפיון, דרך ניסוח הדרישות הטכנולוגיות, ועד לשלב בדיקת הצעות והכרזה על זוכה. תחומי אחריות: ניהול תהליך כתיבת מכרזים טכנולוגיים מורכבים, כולל תכנון, תיאום והוצאה לפועל. אפיון צרכים טכנולוגיים מול לקוחות. ניסוח מסמכי מכרז, מפרטים טכניים, תנאי סף, קריטריונים לקביעת איכות ועוד. עבודה מול גורמים מקצועיים, משפטיים ועסקיים. ליווי תהליכי רכש ציבורי בהתאם לחוק חובת המכרזים ותקנותיו. ביצוע בקרת איכות על מסמכים, ניתוח מכרזים קיימים והפקת לקחים. ייעוץ אסטרטגי בהגשת הצעות למכרזים ממשלתיים וביטחוניים. Requirements דרישות התפקיד: ניסיון של לפחות 15 שנים בכתיבת מכרזים טכנולוגיים, בדגש על מכרזים לגופים ציבוריים. הבנה מעמיקה בטכנולוגיות מידע, תקשורת, מערכות מחשוב ותשתיות. היכרות מלאה עם חוק חובת המכרזים, תקנות הרכש הממשלתי ונהלים רלוונטיים. ניסיון בניהול פרויקטים טכנולוגיים
• יתרון. ניסיון בעבודה מול משרדי ממשלה
• יתרון משמעותי. תואר ראשון חובה
• בתחומים כגון משפטים, הנדסה, מדעי המחשב, תעשייה וניהול, מדיניות ציבורית. תואר שני
• יתרון. יכולת ניסוח גבוהה בעברית ובאנגלית, כולל כתיבה מקצועית של מסמכים מורכבים. ניסיון בעבודה מול לקוחות, ספקים, יועצים משפטיים וגורמים ממשלתיים. יכולת עבודה עצמאית, ניהול זמן ועמידה בלוחות זמנים.

דרישות המשרה

הטכנולוגיות, ועד לשלב בדיקת הצעות והכרזה על זוכה. תחומי אחריות: ניהול תהליך כתיבת מכרזים טכנולוגיים מורכבים, כולל תכנון, תיאום והוצאה לפועל. אפיון צרכים טכנולוגיים מול לקוחות. ניסוח מסמכי מכרז, מפרטים טכניים, תנאי סף, קריטריונים לקביעת איכות ועוד. עבודה מול גורמים מקצועיים, משפטיים ועסקיים. ליווי תהליכי רכש ציבורי בהתאם לחוק חובת המכרזים ותקנותיו. ביצוע בקרת איכות על מסמכים, ניתוח מכרזים קיימים וה

^^משרה זו נלקחה מ Career^^Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr
• accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions. Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University’s career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following: Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required. Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application. Job Title: Clinical Research Coordinator
• CCC | Clinical Trials Office Department: CCC | Clinical Trials Office Position Summary The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Recruitment, Intervention and Survey Shared Resource, a part of the Clinical Trials Office within the Comprehensive Cancer Center at The Ohio State University Wexner Medical Center. Responsibilities Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols Recruit, interview and enroll patients Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements Educate patients and families of purpose, goals, and processes of clinical study Coordinate scheduling and follow
• through of patient care appointments, procedures, & other diagnostic testing in accordance with the study protocol Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication and notifies appropriate clinical professionals to evaluate patient response, identify the status of complications, & provide the appropriate level of care Document unfavorable responses and notify research sponsors & applicable regulatory agencies Assist with collecting, extracting, coding, and analyzing clinical research data Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state, and industry sponsor regulations Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors Participate in activities to develop new research protocols and contributes to the establishment of study goals to meet protocol requirements Job Requirements Bachelor’s Degree in biological sciences, health sciences, social sciences, or other medical field or an equivalent combination of education and experience required. One year of experience in a clinical research capacity is required. Knowledge of medical terminology desired. Clinical research certification from an accredited certifying agency desired. Computer skills required with experience using Microsoft Office Software applications desired. Must be able to effectively communicate, both face
• to
• face and in writing, with clinical staff, research participants, and outside collaborators. Additional Information: As one of only 50 designated comprehensive cancer centers in the nation, The Ohio State University Comprehensive Cancer Center
• Arthur G. James Cancer Hospital and Richard J. Solove Research Institute is dedicated to the creation of knowledge in laboratory, clinical and population
• based cancer research. We apply those discoveries to develop more effective approaches to cancer prevention, diagnosis, and therapies
• providing tomorrow’s standard of care today. A Cancer
• Free World Begins Here. Research and Scholarship
• Clinical Research
• Individual Contributor
• Specialized
• S2 Experienced Location: OSU Gynecologic Oncology (2523) Position Type: Regular Scheduled Hours: 40 Shift: First Shift Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process. Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions. The university is an equal opportunity employer, including veterans and disability. As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression. Each day, Buckeyes across the state and around the world make a lasting impact. The Ohio State University sets the stage for academic achievement and innovation. It’s where friendships are forged, tradition is brought to life and a better global community is built. Our mission is as clear today as it was 150 years ago: to illuminate a pathway to education, research and health care that creates vibrant futures. Faculty and staff build the incomparable Buckeye spirit through collaboration, a strong sense of community and an unwavering commitment to excellence. Our strength comes from our ability to bring out the best in people and learn from Buckeyes of all backgrounds, passions and talents. Ohio State is a dynamic community where opportunity thrives and individuals transform themselves and their world. Positions are available in countless fields and specialties. Ohio State is a top
• 20 public university, and its Ohio State Wexner Medical Center is one of America’s leading academic health centers. Eligible Ohio State employees receive comprehensive benefits packages, including medical, dental and vision insurance, tuition assistance for employees and their dependents, and state or alternative retirement options with competitive employer contributions. Become a Buckeye and contribute to an incredible legacy that serves to guide our future and shape a better tomorrow.

דרישות המשרה

Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols Recruit, interview and enroll patients Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements Educate patients and families of purpose, goals, and processes of clinical study Coordinate scheduling and

^^משרה זו נלקחה מ Career^^Overview Position: Quality Engineer 1 Location: BEN GURION AIRPORT Duration: On
• Going contract Frequency: 40hrs per week Compensation: $60/hr. USD (ILS ₪212.916) Position Overview: Job Description: Utilize quality science techniques to effect continuous performance improvement at assigned suppliers. Reviews, analyzes, and reports on quality discrepancies related to process, assembly, manufacturing, mechanical, electrical, hydraulic, or electro
• mechanical systems. Ensure that performance and quality of products conform to established company and regulatory standards. Use surveillance and auditing techniques to identify opportunities for process and product improvement. Interfaces with manufacturing, engineering, customer, supplier, and procurement (as appropriate) to ensure requirements / expectations are satisfied. Facilitate development of supplier recovery plans. Monitor and evaluate supplier process for compliance to purchase order and engineering requirements. Collaborate with supplier to investigate root cause and corrective actions when process or product deficiencies are detected. Identify, plan, and facilitate cross
• functional improvement activities. Deploy variation management tools and techniques at select suppliers to mitigate risk. Have performed Quality System Audits, AS9102 First Article Reviews. Computer proficiency and proficiency with MS Office products. Additional Comments: Travel is required and may extend beyond the local area. Initial supplier assignments may change to meet customer requirements. Work hours are not fixed or guaranteed and may extend beyond 40 hours per week to meet customer requirements. Aerospace supplier experience is preferred and may be used as the primary selection criteria among equally qualified candidates. Skills Requirement: Experience with large complex airframe assemblies desired. Production (or Manufacturing) Quality Assurance/Control in Aerospace industry (or similar). Ability to interpret blueprints and specifications. Collaborate with production personnel and stakeholders. Identify and drive root cause and corrective actions. Execute on deliveries. Attention to Detail. Strong communication skills. In process and Final Inspection. Requirements: 5+ Years experience in Aerospace Quality engineering Preference for a US Citizen or dual
• citizen. If not a US Citizen, ability to secure a DSP
• 5. 5+ years’ experience in FAI and AS9102 “We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, age, political affiliation, marital status, disability status, protected veteran status, or any other characteristic protected by law. Verify, Inc. will not tolerate discrimination or harassment based on any of these characteristics.”

דרישות המשרה

/ expectations are satisfied. Facilitate development of supplier recovery plans. Monitor and evaluate supplier process for compliance to purchase order and engineering requirements. Collaborate with supplier to investigate root cause and corrective actions when process or product deficiencies are detected. Identify, plan, and facilitate cross
• functional improvement activities. Deploy variation m

^^משרה זו נלקחה מ INDEED^^
לחב’ יצרנית בעולם הטקסטיל והמארזים בפתח תקווה דרוש/ה מבקר/ת איכות. במסגרת התפקיד: עבודה מול מחלקת יצור ביצוע ביקורת סופית ,מילוי דוחות והעברתם ללקוח ועוד. העבודה במשרה מלאה ממשרדי/מפעלי החברה באזור התעשייה סגולה פתח תקווה, בימים א
• ה. ניסיון של שנה בתפקיד דומה ידע בקריאת שרטוטים ידע בהגשת דוחות ביקורת ניסיון על חשבשבת זמינות למשרה מלאה

דרישות המשרה

לא צויין

^^משרה זו נלקחה מ INDEED^^
הובלת פעילויות הנדסת מערכת לפיתוח מוצרים ותכונות חדשים
• הגדרת דרישות ומפרטים עבור יכולות חדשות
• תכנון וביצוע ניסויים ברמת המערכת, ניתוח נתונים והצעת פתרונות מבוססי נתונים
• ציון ובדיקת נהלי בדיקה, אימות ואימות ביצועי מוצר
• הובלת חקירות כשלים, ניתוחי שורש גורמים ושיפורי תכנון מונעים
• פיתוח ויישום כלים לייצור, בקרת איכות וניטור ביצועים
• שיתוף פעולה הדוק עם צוותי הנדסת תוכנה, אלגוריתמים, מכונות וחשמל תואר ראשון בהנדסת חשמל / מדעי המחשב / פיזיקה (מועדף לתואר שני)
• 3+ שנות ניסיון בהנדסת מערכות בסביבה רב
• תחומית (תוכנה, אלגוריתמים, מכניקה, אלקטרוניקה)
• ניסיון מוכח בניתוח נתונים, ניתוח סטטיסטי, הכנת דוחות והצעת פתרונות מבוססי נתונים
• ניסוין מעשי עם כישורי פתרון בעיות חזקים
• בעל מוטיבציה עצמית ועצמאי, עם יכולת לקחת אחריות על משימות
• מהנדס/מדען פתוח, סקרן ורוצה ללמוד
• מאורגן היטב ומסוגל להוביל מספר משימות טכניות מורכבות בו זמנית
• שליטה מלאה באנגלית (בעל פה ובכתב)
• כישורי תקשורת בין
• אישיים ותקשורתיים חזקים

דרישות המשרה

ומפרטים עבור יכולות חדשות
• תכנון וביצוע ניסויים ברמת המערכת, ניתוח נתונים והצעת פתרונות מבוססי נתונים
• ציון ובדיקת נהלי בדיקה, אימות ואימות ביצועי מוצר
• הובלת חקירות כשלים, ניתוחי שורש גורמים ושיפורי תכנון מונעים
• פיתוח ויישום כלים לייצור, בקרת איכות וניטור ביצועים
• שיתוף פעולה הדוק עם צוותי הנדסת תוכנה, אלגוריתמים, מכונות וחשמל תואר ראשון בהנדסת חשמל / מדעי המחשב / פיזיקה (מועדף לתואר שני)
•

^^משרה זו נלקחה מ INDEED^^
מה בתפקיד: ניהול מו”מ עם ספקים בארץ ובחו”ל טיפול בבקשות להצעות מחיר והוצאת הזמנות רכש העברת שרטוטים לספקים בתחומי חומרי גלם, עיבוד שבבי, ציפויים ועוד מעקב אחר מועדי אספקה ואיכות הספקים שיתוף פעולה עם מחלקת אבטחת איכות מה אנחנו מחפשים? ניסיון ברכש טכני
• חובה (יתרון לעיבוד שבבי) ניסיון בעבודה מול לפחות 10 ספקים בחו”ל
• חובה אנגלית ברמה גבוהה
• חובה שליטה בקריאת שרטוטים
• חובה ניסיון מוכח בניהול מו”מ, צמצום עלויות ובניית הסכמים שליטה במערכות ERP
• חובה (יתרון משמעותי ל
• Priority) שליטה גבוהה באקסל
• חובה (כולל נוסחאות, טבלאות, גרפים ופיבוטים)

דרישות המשרה

לא צויין

Control Commissioning Engineer
– come shape the future with us! Knapp is hiring PLC engineers to join our commissioning team, joining and shaping new projects from ground zero! Important information: this position includes a training period abroad (Europe/US), and then joining our new projects in Israel. A little bit about us: Knapp develops and manufactures intelligent warehouse systems using the latest solutions in digitalization, software, automation and robotics. Our mission is to provide our customers with the technologies they need to excel in their industry, with the latest in shuttle technology, AI-infused robotics, all- in one and more. Main tasks: * Independent project preparation * Preparing and carrying out switch cabinet tests, special machines tests and factory tests * Creating, maintaining and improving startup instructions, test protocols and checklists * Supporting the PLC development departments * Independent configuration, startup and test of the components at the customer * Coordinating and supporting tests of third parties and the customer * Carrying out measurements for quality assurance purposes * Direct contact, collaboration and partnership with the customer * Supporting the planning department in new developments * Assisting the startup phase and supporting the customer * Documentation and backup of the components put in operation * Carrying out on-site interventions Job requirements: * In-depth knowledge of Siemens control systems * Technical education (apprenticeship or technical college) * Excellent command of English – spoken and written. * Soft skills: ability to work under pressure, independency, willingness to learn and creativity. * Willingness to travel abroad for the training period.

דרישות המשרה

* In-depth knowledge of Siemens control systems * Technical education (apprenticeship or technical college) * Excellent command of English – spoken and written. * Soft skills: ability to work under pressure, independency, willingness to learn and creativity. * Willingness to travel abroad for the training period.

Product Manager – Electromechanical Products Location: Yavne, Yavne (On-site, Full-Time) Are you a strategic thinker with a passion for cutting-edge technology? Do you have a strong background in electromechanical product development? We are seeking a Product Manager to lead the development of innovative locking solutions and security systems. This role is an exciting opportunity to work with cross-functional teams, from R&D and manufacturing to marketing and sales, ensuring high-quality product development and market success. What You’ll Do: Oversee the product lifecycle from ideation to launch. Collaborate with R&D, production, procurement, and marketing teams. Develop product strategy based on market research and competitor analysis. Ensure product quality through rigorous testing and customer feedback. Support sales and marketing teams with technical expertise and materials. What You Bring: Bachelor’s degree in Computer Engineering, Electrical Engineering, or a related field. 3-5 years of experience in product management for electromechanical products or complex technologies. Strong understanding of manufacturing, supply chain logistics, and quality assurance. Ability to lead cross-functional teams and drive project success. Excellent communication skills in English (written & spoken). Important: This is an on-site role in Yavne (Monday–Friday). Hybrid work is not available for this position. Ready to make an impact? Apply now and be part of an innovative company shaping the future of security technology! *Although this job ad may appear male-oriented, it is open and welcoming to candidates of all genders. ——————————————— מנהל/ת מוצר – מוצרים אלקטרומכניים מיקום: יבנה, ישראל (עבודה מהמשרדים, משרה מלאה) האם יש לך ראייה אסטרטגית ותשוקה לטכנולוגיה מתקדמת? האם את/ה בעל/ת ניסיון בניהול מוצרים אלקטרומכניים? אנו מחפשים מנהל/ת מוצר להובלת פיתוח פתרונות נעילה חדשניים ומערכות אבטחה מתקדמות. זוהי הזדמנות להצטרף לחברה מובילה ולעבוד בשיתוף פעולה עם צוותי פיתוח, ייצור, שיווק ומכירות כדי להבטיח מוצרים איכותיים ושוק מצליח. תחומי אחריות: ניהול מחזור חיי המוצר משלב הרעיון ועד ההשקה. שיתוף פעולה עם צוותי מו”פ, ייצור, רכש ושיווק. פיתוח אסטרטגיית מוצר מבוססת מחקר שוק וניתוח מתחרים. הבטחת איכות המוצר באמצעות בדיקות ובקרת איכות. תמיכה טכנית וסיוע לצוותי מכירות ושיווק. דרישות תפקיד: תואר ראשון בהנדסת מחשבים / חשמל / תחום רלוונטי אחר. 3-5 שנות ניסיון בניהול מוצר בתחום האלקטרומכני או בטכנולוגיות מורכבות. הבנה מעמיקה בתהליכי ייצור, שרשרת אספקה ואבטחת איכות. יכולת הובלת צוותים וניהול פרויקטים חוצי-ארגון. אנגלית ברמה גבוהה (דיבור, קריאה וכתיבה). חשוב לדעת: המשרה מתבצעת מהמשרדים ביבנה (א’-ה’). אין אפשרות לעבודה היברידית. מוכנים לאתגר הבא שלכם? הצטרפו אלינו והשפיעו על עתיד טכנולוגיות האבטחה! *Although this job ad may appear male-oriented, it is open and welcoming to candidates of all genders.

דרישות המשרה

תפקיד: תואר ראשון בהנדסת מחשבים / חשמל / תחום רלוונטי אחר. 3-5 שנות ניסיון בניהול מוצר בתחום האלקטרומכני או בטכנולוגיות מורכבות. הבנה מעמיקה בתהליכי ייצור, שרשרת אספקה ואבטחת איכות. יכולת הובלת צוותים וניהול פרויקטים חוצי-ארגון. אנגלית ברמה גבוהה (דיבור, קריאה וכתיבה). חשוב לדעת: המשרה מתבצעת מהמשרדים ביבנה (א’-ה’). אין אפשרות לעבודה היברידית. מוכנים לאתגר הבא שלכם? הצטרפו אלינו והשפיעו על ע

Head of Supplier Quality | Yehud | IAI – Systems Missiles & Space Division We are looking for a Head of Supplier Quality to lead the supplier quality domain at IAI’s Systems and Engineering Plant, part of the Missiles & Space Division. The position includes:
• Managing and leading the supplier quality field in the plant, including policy, objectives, and process control
• Setting and aligning expectations with suppliers for new orders, including training and ongoing support
• Participating in the selection of subcontractors suited for required activities
• Initiating and leading continuous improvement programs in collaboration with suppliers
• Developing and implementing processes for supplier performance monitoring, evaluation, and measurement
• Managing interfaces with procurement, engineering, and project quality managers
• Presenting ongoing quality status reports to management regarding supplier performance What we’re looking for: Mandatory requirements:
• Israeli citizenship – required
• Bachelor’s degree in engineering or a related academic field – required
• Over 7 years of experience in a manufacturing environment developing and producing electromechanical or electronic assemblies – required
• Proven experience working with subcontractors – required Additional criteria (advantages):
• Experience in transfer from development to production or in engineering
• Experience in quality assurance
• Master’s degree in Quality Assurance
• Strong teamwork skills and broad system perspective Leadership criteria:
• Proven leadership and delegation capabilities
• System-oriented approach with cross-organizational collaboration
• Ability to define and implement business and organizational strategies that drive technological innovation
• Leadership that inspires and drives cultural and organizational change
• Strong business orientation and commitment to success Application details: Applications will be accepted until October 30, 2025, at 16:
00. Submission includes completing the attached questionnaire and meeting all mandatory requirements. Qualified candidates will be invited for a personal interview and, if necessary, suitability assessments. By submitting an application, the candidate agrees to undergo any required evaluations, including a security clearance investigation. The selection committee is not obligated to invite all applicants to interviews or assessments, nor to recommend any specific candidate. This position is open to all genders. Good to know: The Missiles & Space Division develops and delivers cutting-edge systems and products in the fields of missile technology, space, communications, and navigation. We invite you to join us in a diverse and meaningful position that involves leading projects at the forefront of technology, contributing to national security, and becoming part of a supportive, close-knit team that fosters personal and professional growth.

דרישות המשרה

• Israeli citizenship – required
• Bachelor’s degree in engineering or a related academic field – required
• Over 7 years of experience in a manufacturing environment developing and producing electromechanical or electronic assemblies – required
• Proven experience working with subcontractors – required Additional criteria (advantages):
• Experience in transfer from development to production or in