QA Engineer

Requisition ID: 72733Date: Jan 22, 2026Location:Shlomi, ISR, IL Ra'anana, ISR, ILDepartment: QualityDescription: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 SummaryIn this fully onsite role, the Manufacturing Quality Engineer will be own on all activities at one of sub-contractors supports the validation process to the contract manufacturing and provides quality oversight to the engineering department while working within a multi-functional team environment for medical devices. The Manufacturing Quality Engineer will lead projects and tasks, from product validation through transfer to the production and play an active role to ensure products meet quality standards consistent with internal procedures and acceptance criteria. Additionally, this role will identify and implement improvements to the production processes. The Manufacturing Quality Engineer will be the products and production focal point for our sub-contractors and will be responsible for projects related to the production and machines, including training, audits, stop and renew the production.Essential Duties and ResponsibilitiesExhibit a strong “quality first” mentality and ensure that product and quality are held to the highest standard.Meet company and departmental goals in the continuous improvement of all products, services and processes.Work cross-functionally with individuals or extended teams to provide guidance and ensure success of projects.Responsible to write, review and approve pilot documents (including reports).write and approve various department and production procedures and forms.Lead investigation processes for deviations and nonconformities in production and create analysis reports.Responsible to train the sub-contractors according QA procedures and VoE.Supports special processes such as sorting or rework in production.Own on all production activities at one of the subcontractors to ensure manufacturing is held according to West procedures and GMP/GDP standardsResponsible for stopping and renewing production with accordance to West requirements and with MQ manager approval.Manage production relates projects and act as MQ focal point in various internal and external projects- such as Data Integrity, CoPQ, production improvement plans, etc.Provide Quality oversight of validation activities and processes.Lead pilot processes which include change and approval of quality aspects in pilot protocols and reports and assure that pilot processes are conducted according to West guidance and protocols.Attend production pilot meetings as the MQ focal point.EducationB.Sc. in Engineering or Science requiredGraduate degree in Engineering preferredWork ExperienceMinimum 3 years of experience in Medical Device Quality & Productionifecycle. Relevant work history and/or experience may be considered in lieu of degreeExperience with production processes and process controlsExperience with sub contractors interface and meeting customer expectationsExperience with Medical Device, Validation Activities, Risk Management, Product Transfer to productionWorking knowledge of quality systems such as ISO 13485, 21 CFR 820, ISO 14971, MDSAPMust have effective problem solving and interpersonal skillsAbility to work independently, multi-task and thrive in fast-paced environmentProblem solving including root cause failure analysis methodsMust be fully bilingual in English/HebrewPreferred Knowledge, Skills and AbilitiesPrevious experience with MasterControl, Share Point, Teamcenter- a plusAdaptable to changes in the work environment, manage competing demands and deal with frequent change, delays or unexpected events.Must maintain the ability to work well with others in a variety of situationsMaintain high attention to detail, accuracy, and overall quality of workMust be able to multi-task, work under time constraints, problem solve, and prioritizeObserve and interpret situations, analyze and solve problemsEffectively communicate and interface with various levels internally and with customersCertified auditor- a plusRelevant work history and/or experience may be considered in lieu of degreeTravel Requirements10%: Up to 26 business days per yearWest 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