Pharma Manufacturing QA
1,629 open positions
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Senior Manager, Regulatory Affairs Process Excellence AbbVieNorth Chicago, IL, us 1mo Manage Regulatory Affairs issue and CAPA systems, triage compliance issues, and drive process improvements to ensure inspection-ready operations.
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Quality Specialist↗ Leo Pharma UK/IeCork, County Cork, Ireland 1mo Support API Manufacturing by ensuring compliance with cGMP and regulatory requirements, managing batch releases, and driving quality investigations.
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Specialist Quality Assurance GMP (m/w/d) engineering people GmbHUlm, Donau, BADEN_WUERTTEMBERG 1mo Ensuring GMP compliance by reviewing and approving manufacturing, packaging, and batch documentation, investigating deviations, and managing corrective actions.
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QA Auditor I ThermofisherAthlone, Ireland 1mo Conduct routine client, internal, and GxP audits to ensure compliance and excellence in clinical auditing processes.
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Chemical/Pharmaceutical, Quality Assurance (NIGHTS) CardinalhealthNM-Albuquerque PET, US $69k–$88k1mo Develop and implement a compliant quality system to assure PET radiopharmaceutical products are reliable, safe, and effective for patient treatment.
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Quality Associate SanofiSeoul, KR 1mo Manage product technical complaints, quality events, and regulatory interactions to ensure compliance and timely resolution.
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Regional Quality Manager (PDx) ANZ GehcAUS08-01-Sydney-241 O'Riordan Street, 8F, AU 1mo Establish, maintain, and continuously improve the Quality Management System (QMS) for Pharmaceutical Diagnostics across Australia and New Zealand, ensuring regulatory compliance and patient safety.
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Global Quality Compliance Inspection Readiness & EMEAC Audits GaldermaBarcelona, ES 1mo Lead global Quality Compliance Inspection Readiness and EMEAC Audits for a dermatology company, ensuring preparedness for regulatory inspections across cosmetics, medical devices, and pharmaceuticals.
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QA Project Manager EvonikLafayette, IN, US 1mo Interface between Quality Assurance, Customers, and Project Managers to ensure customer requirements are met and apply regulatory guidance to new processes.
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Expert qualité MTI - CDI - H/F PierrefabreHaute Garonne (31), FR 1mo Ensure quality and compliance of innovative therapy drugs (MTI) manufactured in-house or outsourced, managing third-party quality processes and crisis management.
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QA Specialist, I PciservicesBedford, NH, USA 1mo Ensure product quality and compliance with internal procedures and external standards through batch record review, deviation management, and quality system oversight.
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Quality Systems Document Coordinator - Casa Grande, AZ AbbottUnited States - Arizona - Casa Grande 1mo Manage controlled documentation, document change control, batch calculations, and quality system records to support manufacturing operations.
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GCP Auditor (Freelance)↗ Adamas ConsultingRemote 1mo Conducting GCP audits, quality assurance projects, and inspection preparation for pharmaceutical and biotechnology companies.
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Quality Assurance Manager Toll GroupNew South Wales 1mo Lead quality systems and compliance programs for healthcare logistics operations, ensuring regulatory adherence and operational excellence.
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Quality Assurance Manager*in - GMP (m/w/d) Lgc-GroupKulmbach, BY, de 1mo Ensure quality assurance in a GMP-controlled laboratory and support the release of therapeutic molecules.
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Director Quality Transformation & Site Excellence↗ Grünenthal GroupLisbon, Lisbon, Portugal 1mo Lead quality assessments, diagnostics, and transformation programs across manufacturing sites to ensure products meet highest quality standards and regulatory compliance.
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Senior QA Compliance Specialist LonzaNL - Geleen €47k–€65k1mo Maintain and strengthen the Quality Management System (QMS) and ensure GMP compliance at a pharmaceutical manufacturing site.
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Qualified Person and Quality Assurance Operations Team Lead NovartisBaarle Nassau, NL €56k–€104k1mo Act as the Qualified Person to ensure compliant certification and release of medicinal products while leading a Quality Assurance team.
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Biologe (m/w/d) DKMS Life Science Lab gGmbHDresden, SACHSEN 1mo Developing and maintaining the Quality Management System (QMS) for a stem cell collection center, ensuring compliance with international regulations and supporting internal/external audits.
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Quality Assurance Manager*in - GMP (m/w/d) Axolabs GmbHKulmbach, BAYERN 1mo Ensure quality assurance in a GMP control laboratory and support the GMP-compliant release of therapeutic molecules.
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Pharma COE QMS Director BdxUSA AZ - Tempe Headquarters 1mo Owns and executes central Quality Management System (QMS) processes and strategy for a global pharmaceutical network, ensuring compliance with GxP regulations and driving quality system standardization across sites and partners.
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Qualitätsingenieur Wareneingangskontrolle (m/w/d) West Pharmaceutical Services Deutschland GmbH & Co. KGEschweiler, Rheinland, NORDRHEIN_WESTFALEN €60k1mo Ensuring quality of raw materials and packaging components for injectable drug manufacturing through incoming inspection, supplier management, and audit execution.
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Sr Director, Quality GileadIreland - Cork 1mo Lead global Quality Assurance (QA) operations and strategy for Gilead's distribution network across multiple international regions, ensuring GMP/GDP compliance and managing product recall readiness.
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Compliance Manager (gn) Bankpower GmbHMünchen, BAYERN 1mo Implementing and developing a Compliance Management System, conducting internal and external audits, and ensuring adherence to national and international regulations (e.g., GxP, AMG, EU-GMP) for a pharmaceutical client.
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Research Projects Coordinator PHSAVictoria, Victoria $69k1mo Coordinate and administer the Quality Management System for the Cancer Immunotherapy Program, ensuring GMP compliance and supporting the production of CAR-T cells.
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Absolwent Kierunków Farmaceutycznych, Biotechnologicznych, Chemicznych lub Biologicznych Ścieżka Rozwoju do QP - Qualified Person AirproductsKedzierzyn-Kozle, Poland 1mo Support the Pharmaceutical Quality System and regulatory processes for medicinal gases, preparing documentation for Qualified Person (QP) release.
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Experienced QA Specialist PolyPeptide SwedenMalmö, SE 1mo Lead auditor and quality system specialist ensuring compliance with EU-GMP regulations for non-sterile API manufacturing.
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CDI - Responsable Qualité site Chamant - Parfums Beauté - H/F/X CcChamant, FR 1mo Site Quality Director responsible for releasing finished makeup batches, managing a team of 4 managers overseeing 60+ people, and ensuring site compliance with pharmaceutical good practices for OTC products.
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Director of Quality CatalentStrathroy-Adair, Canada $140k–$190k1mo Lead Commercial Quality Assurance and Quality Control activities for a new pharmaceutical manufacturing facility, ensuring cGMP compliance and regulatory approval for fast-dissolve oral dosage forms.
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Specialist (m/w/d) Quality Oversight Quality Control Simtra Deutschland GmbHHalle (Westfalen), NORDRHEIN_WESTFALEN 1mo Central interface between Quality Control and Quality Assurance ensuring GMP compliance and effective Quality Oversight in sterile injectable drug manufacturing.
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Associate Specialist, Quality Operations MyhrabcBogota, Colombia 1mo Ensure local compliance with World Courier policies and procedures, coordinate audits, and manage quality systems for pharmaceutical logistics and depot operations.
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Director, Head of Compliance BmsSummit West - NJ - US $188k–$227k1mo Director of Quality Compliance responsible for developing, implementing, and maintaining high standards of quality compliance at a CAR T cell therapy manufacturing facility.
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Senior Specialist, Quality Assurance & Regulatory Affairs BaxterPetaling Jaya, Selangor, MY 1mo Local implementation of regulatory and quality activities, obtaining marketing authorizations for drugs, biologics, and medical devices, and managing product complaints/recalls in Malaysia.
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Quality & Regulatory Affairs Specialist Maneuver MarketingSingapore 1mo Technical backbone for Product Operations, overseeing production quality, stability testing, and regulatory compliance for DTC health supplement brands.
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Director, Head of Compliance BristolmyerssquibbSummit West - NJ - US $188k1mo Director of Quality Compliance leading site compliance programs, audits, and regulatory readiness for a CAR T cell therapy manufacturing facility.
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QA vor Ort Verantwortlicher Formgebung (alle Geschlechter) BayerWeimar,Thuringia,Germany 1mo Conduct process observations and GEMBA walks, provide QA oversight for GMP-relevant change processes, and evaluate events, deviations, and complaints regarding product quality impact.
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Manufacturing Compliance Specialist SeptodontCambridge (Canada) 1mo Conduct investigations into manufacturing deviations, identify root causes, and manage corrective and preventative actions (CAPA) to ensure compliance with GMP standards.
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Profesional de Apoyo Técnico EurofinsBogotá, Bogota, co 1mo Provide technical and regulatory support to the Technical Directorate by managing stability studies, technical documentation, regulatory requirements, and scientific data analysis to ensure compliance with quality standards and applicable regulations.
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