Job Description
QA Engineer
Requisition ID:
71494
Date:
Nov 26, 2025
Location:
Shlomi, ISR, IL
Department:
Quality
Description:
At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
**Job Summary**
***This position is a backfill for maternity leave***
In this fully onsite position that is located in Shlomi, Israel, you will be responsible to control all Quality functions including the expansion and maintenance of the Quality System, provide support for product and process improvements by collecting, compiling, and analyzing inspection and process date, and ensure the effective use of resources to meet site quality requirements.
**Essential Duties and Responsibilities**
+ QA focal point for engineering projects.
+ Provide guidance on documentation structures and formats to ensure compliance to procedures, relevant regulations, and standards.
+ Responsible for approval of engineering documentation - reviewing and approving technical, mold, test method, equipment and process validation (IQ, OQ, PQ) documentation.
+ Finding solutions for queries within responsibility limits.
+ Assist and provide guidance on any out of specification result, deviation, or excursion that may occur.
+ QA representative in equipment development design reviews
+ QA representative in equipment and process validation reviews.
+ Work cross-functionally with individuals and project or extended teams to provide guidance and ensure success of projects.
+ Attend program meetings as required as part of extended program teams.
+ Provide support, when necessary with review and approval of product development DHF documentation (DDP, PRD, TMX, URS, design verification & validation activities, dFMEA, pFMEA, FMEA risk documents, test methods, OOSs, protocols, reports, product design transfer)
+ Support other QA dept activities, routine sterility validation maintenance activities (dose audit and bioburden), calibration etc
**Education**
B.Sc. in Science or Engineering required
**Work Experience**
+ Minimum 2 years of experience in Medical Device Quality & Product Development Lifecycle
+ Experience in Medical Device / Pharma industry
+ Experience with Medical Device Design & Development, Verification Activities, Risk Management, Product Transfer, DHF Activities
+ Experience in Equipment Validation, Process Validation, Change Control Process
+ Strong working knowledge of quality systems such as ISO 13485, 21 CFR 820, ISO 14971
**Preferred Knowledge, Skills and Abilities**
+ Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
+ Support and contribute to Lean Sigma programs and activities towards delivery of the set target
+ Able to comply with the company’s safety policy at all times
+ Able to comply with the company’s quality policy at all times.
+ Technical skills
+ Written and verbal expression skills: Hebrew- Excellent, English- Excellent
+ Relevant work history and/or experience may be considered in lieu of degree.
**Travel Requirements**
10%: Up to 26 business days per year
**Physical Requirements**
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
**Additional Requirements**
+ Must maintain the ability to work well with others in a variety of situations.
+ Must be able to multi-task, work under time constraints, problem solve and prioritize.
+ Self-motivated with the ability to make independent and sound judgments.
+ Read and interpret data, information, and documents
+ Learn and apply new information or skills
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening.
\#LI-KR1
\#LI-Onsite
Requisition ID:
71494
Date:
Nov 26, 2025
Location:
Shlomi, ISR, IL
Department:
Quality
Description:
At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
**Job Summary**
***This position is a backfill for maternity leave***
In this fully onsite position that is located in Shlomi, Israel, you will be responsible to control all Quality functions including the expansion and maintenance of the Quality System, provide support for product and process improvements by collecting, compiling, and analyzing inspection and process date, and ensure the effective use of resources to meet site quality requirements.
**Essential Duties and Responsibilities**
+ QA focal point for engineering projects.
+ Provide guidance on documentation structures and formats to ensure compliance to procedures, relevant regulations, and standards.
+ Responsible for approval of engineering documentation - reviewing and approving technical, mold, test method, equipment and process validation (IQ, OQ, PQ) documentation.
+ Finding solutions for queries within responsibility limits.
+ Assist and provide guidance on any out of specification result, deviation, or excursion that may occur.
+ QA representative in equipment development design reviews
+ QA representative in equipment and process validation reviews.
+ Work cross-functionally with individuals and project or extended teams to provide guidance and ensure success of projects.
+ Attend program meetings as required as part of extended program teams.
+ Provide support, when necessary with review and approval of product development DHF documentation (DDP, PRD, TMX, URS, design verification & validation activities, dFMEA, pFMEA, FMEA risk documents, test methods, OOSs, protocols, reports, product design transfer)
+ Support other QA dept activities, routine sterility validation maintenance activities (dose audit and bioburden), calibration etc
**Education**
B.Sc. in Science or Engineering required
**Work Experience**
+ Minimum 2 years of experience in Medical Device Quality & Product Development Lifecycle
+ Experience in Medical Device / Pharma industry
+ Experience with Medical Device Design & Development, Verification Activities, Risk Management, Product Transfer, DHF Activities
+ Experience in Equipment Validation, Process Validation, Change Control Process
+ Strong working knowledge of quality systems such as ISO 13485, 21 CFR 820, ISO 14971
**Preferred Knowledge, Skills and Abilities**
+ Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
+ Support and contribute to Lean Sigma programs and activities towards delivery of the set target
+ Able to comply with the company’s safety policy at all times
+ Able to comply with the company’s quality policy at all times.
+ Technical skills
+ Written and verbal expression skills: Hebrew- Excellent, English- Excellent
+ Relevant work history and/or experience may be considered in lieu of degree.
**Travel Requirements**
10%: Up to 26 business days per year
**Physical Requirements**
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
**Additional Requirements**
+ Must maintain the ability to work well with others in a variety of situations.
+ Must be able to multi-task, work under time constraints, problem solve and prioritize.
+ Self-motivated with the ability to make independent and sound judgments.
+ Read and interpret data, information, and documents
+ Learn and apply new information or skills
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening.
\#LI-KR1
\#LI-Onsite
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