C&Q Technician

Kenvue Is Currently Recruiting For A:C&Q TechnicianWhat We DoAt Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.Who We AreOur global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.Role Reports To:SA Engineering and Reliability Campus LeaderLocation:Europe/Middle East/Africa, South Africa, Gauteng, JohannesburgWork Location:Fully OnsiteWhat You Will DoC & Q technicianThis position reports into Engineering & Reliability Leader and is based in Cape Town, South Africa.What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.Who We AreOur global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.Role reports to: SA Engineering Campus LeadLocation: Cape Town, South AfricaTravel %: MinimalPay: 24What You Will DoWhat you will doThe Commissiong & Qualification technician is responsible for generating and maintaining the validation plan in line with GMP and successfully carry out on all Facilities, Utilities (HVAC, Water, Compressed Air and other), Equipment, Systems.Key Responsibilities:Development of User Requirement SpecificationsDevelopment and execution of System Impact Assessments and Component Impact AssessmentsDevelopment and execution of Validation Risk Assessments and Design ReviewsDevelopment and execution of Design Qualifications, Installation Qualifications, Operational Qualifications and Performance Qualifications taking a System Lifecycle ApproachPerform Commissioning (includes Factory Acceptance Testing and Site Acceptance Testing) as required and liaise with other departmentsValidation of Automated SystemsPerform periodic reviews for Equipment, Facilities, Utilities, SystemsRe-qualification of Equipment, Facilities, Utilities, SystemsInteract with all areas and levels of the company in addition to regulatory agencies, vendors, consultants, contractors and other intended partiesFollow and review site validation/qualification SOP’s to ensure they are in line with current compliance requirements from corporate and regulatory authoritiesParticipate in corporate, regulatory and internal auditsMaintain up to date knowledge of corporate and regulatory standardsManage and maintain company validation plan and ensure validation/ qualification activities are successfully carried outMaintain the Validation Master Plan schedule and Validation SystemRequired QualificationsWhat we are looking forRelevant Degree in Life Science/Chemistry/Math (Not necessarily from Biology/Microbiology) or equivalent3-5 years’ experience of qualification/validation in a Pharmaceutical companyExperience with cGMP, cGEP, cGDPStrong problem-solving skills and documentation experience preferredStrong organizational and time management skills.Qualifications background.Desired QualificationsVery strong Quality Analytics knowledge and understanding (ISO / FMEA / HAZOP etc.)Demonstrated knowledge of working within a quality management system and cGMP and regulations 21 CFR 211, EU Annex 11 and 21 CFR Part 11Must have knowledge of Deviations, Investigations, Change Control, CAPA and Risk Assessments within the Pharmaceutical Industry quality systemMust have basic Protocol and execution and Report writing skillsAbility to work independently and as part of a teamProficiency in relevant software and toolsProficiency in Microsoft Office, including Word, PowerPoint, and Excel.What’s In It For YouCompetitive Benefit PackageLearning & Development OpportunitiesKenvuer Impact NetworksThis list could vary based on location/regionKenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.