Pharma Manufacturing QA
1,629 open positions
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Compliance Officer FreseniusglobalMelrose Park, IL, US $80k13d Administers and maintains Quality Systems at a production unit from an FDA and global perspective, leading investigations into deviations and complaints to ensure regulatory audit readiness.
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Director, Product Quality Small Molecule GileadUnited States - California - Santa Monica $191k–$248k13d Lead product quality strategy, risk assessment, and regulatory compliance for small molecule drug development and manufacturing.
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QA Manager and QP↗ Sandoz UK & IrelandBracknell, England, UK 13d Lead local execution of quality systems and GxP compliance for a biosimilar and generic medicine manufacturer, acting as the Qualified Person (QP) for batch release and regulatory oversight.
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Specialist Quality Assurance (m/w/d) AbbottGermany - Neustadt am Rübenberge 13d Ensuring quality of pharmaceutical raw materials and animal by-products through documentation control, quality inspection, and usage decisions.
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Senior Specialist, QA Compliance BmsCruiserath - IE 13d Senior Specialist ensuring data integrity, AI governance, and supplier quality compliance for biologics manufacturing operations.
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Quality Manager↗ Bestway Healthcare UKRedditch, England, UK 13d Ensuring regulatory compliance, quality assurance, and continuous improvement for wholesale pharmaceutical operations (Specials and Parallel Imports) while acting as the Responsible Person.
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Senior Specialist QAC Materials Management↗ Bristol Myers Squibb UK & IrelandCounty Dublin, Ireland 13d Support material qualification and release activities for biologic commercial and clinical pipelines at the Cruiserath manufacturing facility.
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Senior Specialist QAC Materials Management↗ Bristol Myers SquibbCounty Dublin, Ireland 13d Support material qualification and release activities for biologic commercial and clinical pipelines at the Cruiserath manufacturing facility.
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Quality Assurance - Corporate Consultant↗ QbD GroupBarcelona, Catalonia, Spain 13d Manage the GxP Training System for a life sciences client, ensuring compliance with Quality, Safety, and regulatory requirements.
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Quality and Regulatory Affairs Auditor Jr - Buenos Aires↗ TransPerfectBuenos Aires Province, Argentina 13d Conduct internal, customer, supplier, and regulatory audits to support and enhance the Global Quality Management System (QMS) in the Life Sciences industry.
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Senior QA Drug Substance Operations Specialist↗ WuXi BiologicsDundalk, County Louth, Ireland 13d Provide online QA oversight to Drug Substance manufacturing operations, ensuring compliance with cGMP and SOPs while supporting daily manufacturing activities.
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Coordenador de Qualidade↗ JobbolSão Paulo, São Paulo, Brazil 13d Leading the Quality area and developing teams to ensure compliance with ANVISA, sanitary legislation, and Good Manufacturing Practices (GMP) in the cosmetics and perfumery industry.
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Sr Administrative Service Coordinator ThermofisherGreenville, North Carolina, USA 13d Provide administrative and operational support in a GMP environment, including document control, compliance management, and inventory coordination for pharmaceutical manufacturing.
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Batch Release Lead↗ SanofiSingapore, Singapore 13d Provide Quality Assurance oversight for final drug substance disposition, batch release, deviation management, change control, and Product Quality Review activities to ensure compliance with GMP and regulatory standards.
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Analista de Qualidade↗ VtclogBrasília, Federal District, Brazil 13d Plan, execute, and monitor Quality Management System activities to ensure process compliance with standards, internal procedures, and legal requirements.
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Analista de Documentación Senior↗ Jlm Projects 13d Senior Quality Assurance/Documentation Analyst responsible for managing internal and external documentation, change control, and validation within a pharmaceutical manufacturing facility.
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Lead : Clinical Quality Assurance (FSP)↗ Tech ObserverMumbai, Maharashtra, India 13d Lead clinical quality assurance audits and ensure compliance with ICH GCP, protocols, and regulatory requirements for clinical trials.
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Quality & Regulatory Affairs Group Manager↗ I-Pharm ConsultingBrisbane, Queensland, Australia 13d Establish strategic direction for the Pharmaceutical Quality System, oversee product quality and patient safety, and manage regulatory compliance across all sites and outsourced activities for a medicinal cannabis manufacturer.
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Quality Assurance Supervisor↗ JC Green Inc.Thorndale, ON, CA $55k–$65k13d Support quality assurance across cultivation, processing, extraction, and packaging operations in a regulated cannabis production environment.
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Higher / Executive - QA↗ St LogisticsJurong Island, S00, SG 13d Manage customer relationships, drive continuous improvement in product quality, and execute quality control activities for pharmaceutical and healthcare supply chain operations.
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Quality Control Analyst↗ EpicurMount Laurel, NJ, US 13d Ensuring quality of materials and finished drug products are manufactured to meet cGMP and Epicur Pharma standards.
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PQR & PQE Specialist↗ ZentivaAnkleshwar, Gujarat, India 13d Prepare, compile, and perform first-level review of Product Quality Reviews (PQR) to ensure data completeness, accuracy, and traceability for pharmaceutical affiliates and CMOs.
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Regulatory Affairs Specialist↗ Imaging EndpointsHyderabad, Telangana, India 13d Assist management in executing day-to-day tasks to manage, maintain, and improve regulatory systems to meet regulatory requirements for clinical trials and investigational products.
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Quality Assurance Manager / QP↗ AccproDublin, County Dublin, Ireland 13d Lead Quality Assurance and Quality Control operations at a pharmaceutical manufacturing site, ensuring compliance with EU GMP and HPRA requirements while driving a culture of quality excellence.
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Senior Quality Assurance Specialist - Digital Apps (CVRM) RocheHolly Springs, US $94k–$175k13d Senior Quality Assurance Specialist ensuring digital systems compliance, configuration, and maintenance for aseptic drug product manufacturing.
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Lead Auditing QA Specialist LonzaUS - Tampa, FL 13d Lead planning and execution of audits for products and processes to ensure GMP compliance and quality in pharmaceutical manufacturing.
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Associate Manager-Quality Investigation PfizerIndia - Vizag 13d Lead independent reviews and challenge of microbiological deviations, OOS/OOT, contamination, and sterility assurance investigations to ensure scientific robustness and regulatory compliance.
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Senior Executive Aveva Drug Delivery SystemsBalanagar, Hyderabad 13d Senior executive responsible for Quality Assurance in a pharmaceutical laboratory, managing document control, SOP approvals, change control, deviations, and internal audits for OSD and injectable products.
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Analista de Calidad – Industria Farmacéutica SgsBuenos Aires, Cdad. Autónoma de Buenos Aires, ar 13d Support the Quality area to ensure compliance with GMP, internal procedures, and applicable regulatory requirements, contributing to the maintenance and improvement of the Quality Management System.
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Director, Quality Control Operations VaxcyteVisp, Switzerland 14d Leads QC Operations team and ensures compliant, inspection-ready quality control execution across contract manufacturing and testing networks for vaccine products.
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Senior Quality Manager - Systems & Compliance MeiragtxLondon 14d Maintaining and continuously improving GxP Quality Systems to ensure inspection readiness and providing ongoing support and training to functions across MeiraGTx.
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Senior Quality Engineer West Pharmaceutical ServicesJurong Town, West 14d Provide end-to-end quality oversight and partnering to ensure alignment with stakeholders, customers, and patient expectations in a pharmaceutical manufacturing environment.
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Regulatory Affairs Associate II Teva PharmaceuticalsNavi Mumbai, Maharashtra 14d Prepare, review, and submit high-quality regulatory submissions to the FDA, including Annual Reports, supplements, and post-approval changes.
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External Quality Operations Manager SobiStockholm, Stockholm County, se 14d Main quality contact for Contract Manufacturing Organizations (CMOs), overseeing external manufacturing quality and acting as a Qualified Person (QP) delegate for EU batch release.
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Coordinateur Assurance Qualité Fed GroupFrance 14d Coordinateur Assurance Qualité supporting product and process compliance, risk analysis, and continuous improvement in a growing pharmaceutical industry.
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QA Specialist Adecco ItaliaEboli, Provincia di Salerno 14d Ensures compliance with cGMP and safety regulations for sterile pharmaceutical production by managing QA activities, reviewing batch records, and handling deviations.
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Quality Specialist I↗ Labconnect, LLCJohnson City, TN, US 14d Assists Quality Management in monitoring GCP regulatory compliance and quality in clinical trial operational activities for pharmaceutical and biotech clients.
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Associate Director ESP Quality NovartisLondon (The Westworks), GB £64k–£119k14d Liaison between Novartis clinical trial teams and Third Parties to provide expert QA support during due diligence, qualification, and ongoing governance of technology-enabled services.
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Quality Assurance Technician↗ GaldermaUppsala, Uppsala County, Sweden 14d Quality Assurance Technician supporting biologics manufacturing operations in Uppsala, ensuring compliance with GMP and quality standards.
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Senior Manager, Country Quality (Canada) AstraZenecaMississauga, Ontario, Canada $88k–$116k14d Manage the Corporate Quality Management System (QMS) and ensure compliance with Health Canada GMP requirements for product release and manufacturing operations.
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Manager, QA - Doc Control↗ PCI Pharma ServicesBedford, NH, US 14d Lead the QA Document Control team across multiple production facilities to manage the lifecycle of GMP-controlled documents, procedures, and records, ensuring compliance with regulatory requirements.
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Associate Director, Country Quality, Germany (m/w/d)↗ ModernaMünchen, BY, DE 14d Lead Quality governance and regulatory compliance for Moderna's German commercial operations, serving as the statutory Responsible Person (RP/RPi) for wholesale distribution of mRNA medicines.
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