{"schemaVersion":"jobsearcher.job.v1","id":"e8d7d79cb32fd3efd39d8a95","url":"https://jobsearcher.com/jobs/e8d7d79cb32fd3efd39d8a95","canonicalUrl":"https://jobsearcher.com/jobs/e8d7d79cb32fd3efd39d8a95","title":"CAPA Sr. Associate","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\n\nCAPA Sr. Associate\n\nThe CAPA Sr. Associate will support nonconformance investigations, CAPA activities, root cause analysis, technical documentation, and effectiveness checks within a regulated pharmaceutical or medical device manufacturing environment.\n\nDescription:\n\nExecute and document nonconformance investigations, including identification of root, probable, potential, and contributing causes.\nDevelop investigation strategies through multidisciplinary collaboration, process observations, product/sample evaluations, interviews, and follow-up activities.\nPrepare clear technical reports, including investigation plans, executive summaries, testing strategies, root cause hypotheses, and investigation results.\nApply Root Cause Analysis tools and coordinate with SMEs to obtain scientific and technical input.\nSupport identification and implementation of mitigation actions, Corrective and Preventive Actions, and Effectiveness Check criteria.\nPartner with Investigation and CAPA approvers to support timely execution and closure of records.\nParticipate in CAPA review boards and continuous improvement initiatives.\nProvide coaching, mentoring, and guidance related to Nonconformance and CAPA processes.\nPromote compliance with applicable EHS practices and a zero-harm workplace.\n\nQualifications:\n\nBachelor’s degree in Engineering, Science, or a related field.\nMinimum 5 years of experience in the pharmaceutical, drug manufacturing, or medical device industry.\nMinimum 3 years of experience in a similar role or responsibility; 5+ years preferred.\nMinimum 3 years of supervisory experience; 5+ years preferred.\nStrong knowledge of Quality Systems and Good Manufacturing Practices (GMP).\nTrackWise experience preferred.\nStrong analytical, problem-solving, leadership, communication, influencing, and negotiation skills.\nFluent in written and spoken English.\nBilingual English/Spanish.\nAbility to work effectively within multidisciplinary teams.\nWillingness to travel occasionally.\n\nPhysical Requirements\n\nLight work, including occasional lifting of up to 20 lbs and the ability to walk, stand, or perform other physical activities associated with a manufacturing environment.\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","company":"Validation","rawCompany":"validation","city":"Toms River","state":"NJ","isRemote":false,"isActive":false,"createdAt":"2026-09-10T10:43:07.969Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"CAPA Sr. Associate","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\n\nCAPA Sr. Associate\n\nThe CAPA Sr. Associate will support nonconformance investigations, CAPA activities, root cause analysis, technical documentation, and effectiveness checks within a regulated pharmaceutical or medical device manufacturing environment.\n\nDescription:\n\nExecute and document nonconformance investigations, including identification of root, probable, potential, and contributing causes.\nDevelop investigation strategies through multidisciplinary collaboration, process observations, product/sample evaluations, interviews, and follow-up activities.\nPrepare clear technical reports, including investigation plans, executive summaries, testing strategies, root cause hypotheses, and investigation results.\nApply Root Cause Analysis tools and coordinate with SMEs to obtain scientific and technical input.\nSupport identification and implementation of mitigation actions, Corrective and Preventive Actions, and Effectiveness Check criteria.\nPartner with Investigation and CAPA approvers to support timely execution and closure of records.\nParticipate in CAPA review boards and continuous improvement initiatives.\nProvide coaching, mentoring, and guidance related to Nonconformance and CAPA processes.\nPromote compliance with applicable EHS practices and a zero-harm workplace.\n\nQualifications:\n\nBachelor’s degree in Engineering, Science, or a related field.\nMinimum 5 years of experience in the pharmaceutical, drug manufacturing, or medical device industry.\nMinimum 3 years of experience in a similar role or responsibility; 5+ years preferred.\nMinimum 3 years of supervisory experience; 5+ years preferred.\nStrong knowledge of Quality Systems and Good Manufacturing Practices (GMP).\nTrackWise experience preferred.\nStrong analytical, problem-solving, leadership, communication, influencing, and negotiation skills.\nFluent in written and spoken English.\nBilingual English/Spanish.\nAbility to work effectively within multidisciplinary teams.\nWillingness to travel occasionally.\n\nPhysical Requirements\n\nLight work, including occasional lifting of up to 20 lbs and the ability to walk, stand, or perform other physical activities associated with a manufacturing environment.\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","datePosted":"2026-09-10T10:43:07.969Z","dateModified":"2026-09-10T10:43:07.969Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Toms River","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e8d7d79cb32fd3efd39d8a95"},"url":"https://jobsearcher.com/jobs/e8d7d79cb32fd3efd39d8a95"}}