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Healthcare
› Pharma Manufacturing QA
Pharma Manufacturing QA
1,629 open positions
Senior Executive-QA
Piramal Pharma
India
19d
Reviewing audit trails and releasing analytical data for intermediates, finished products, and stability batches in a pharmaceutical CDMO.
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Manager / Senior Manager, Quality Assurance
Arspharmaceuticalsoperationsinc
Corporate HQ
$145k
19d
Own batch disposition and product complaint management for products made at contract manufacturing organizations (CMOs) to ensure cGMP and regulatory compliance.
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Manager, QC
West Pharmaceutical Services Singapore Pte Ltd
Singapore
19d
Lead the Quality Control team to oversee mold monitoring, incoming material control, in-process and finished goods inspection, and batch release activities in a cGMP manufacturing environment.
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Leitung Warenmanagement (m/w/d)
ABF-Pharmazie GmbH & Co. KG
Remote
€55k
20d
Lead the pharmaceutical goods management department, ensuring compliant storage and distribution of medicines and medical devices.
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Quality Assurance Manager* (m/w/d)
Lgc-Group
Berlin, BE, de
20d
Build and develop a GMP-compliant Quality Management System (QMS) for a Life Science company, ensuring adherence to high quality standards and international regulations.
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QA Cryo Supervisor CAR-T
Johnson and Johnson
Beerse, Turnhout
€60k–€96k
20d
Leads a team of QA Associates Cryo to ensure sustainable EMEA CAR-T Quality Assurance operations at the Beerse Cryopreservation Center.
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QA Cryo Lead
Johnson and Johnson
Beerse, Turnhout
€73k–€115k
20d
Lead Quality Assurance for CAR-T cell therapy cryopreservation operations, ensuring compliance and operational continuity in the EMEA region.
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Senior Clinical QA Specialist
Edetek
Remote
20d
Senior QA specialist ensuring compliance and quality across biometric services and computer systems through audits, risk management, and system validation.
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Lead Quality Dossier Program Auditor
AbbVie
North Chicago, IL, us
20d
Plan and conduct audits for clinical, pre-clinical, and CMC documents within the Quality Dossier Program to ensure regulatory compliance.
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Director, Clinical Quality
↗
Viking Therapeutics, Inc.
San Diego, CA, US
20d
Lead the Clinical Quality Assurance function and provide strategic leadership and hands-on quality oversight across early- through late-stage clinical development programs.
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Senior Manager, Product Complaints
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Resilience
West Chester, OH, US
20d
Own the product complaints program to ensure timely evaluation, investigation, and closure of product quality complaints in compliance with GMP, regulatory, and company requirements, driving continuous improvement in product quality and patient safety.
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Manager / Senior Manager, Quality Assurance
↗
San Diego, CA, US
$145k
20d
Own batch disposition and product complaint management for products made at contract manufacturing organizations (CMOs) to ensure cGMP and regulatory compliance.
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Senior Quality System Specialist
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Wuxi Xdc Singapore Private Limited
Tanjong Pagar, S00, SG
20d
Senior-level quality and compliance expert ensuring GMP compliance and driving continuous improvement of the Quality Management System (QMS) across the pharmaceutical product lifecycle.
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Senior CMO Manager, External Manufacturing
↗
Bavarian Nordic
Remote
$150k–$195k
20d
End-to-end management of Contract Manufacturing Organization (CMO) activities to ensure reliable, compliant, and timely delivery of vaccine manufacturing.
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Quality Compliance Lead
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Wuxi Xdc Singapore Private Limited
Tanjong Pagar, S00, SG
20d
Lead site Quality Compliance function to ensure GMP inspection readiness across all quality systems and operations.
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QA Lead
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High Ground Medica Inc.
Oyen, AB, CA
20d
Owns the system side of the Quality Management System (QMS) including training, document control, quality event administration, supplier qualification, audits, and batch record review for a regulated cannabis/pharmaceutical environment.
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Lead Quality, HCM
↗
Acg Worldwide
MH, IN
20d
Lead Quality, HCM role responsible for ensuring products meet quality standards, driving start-to-end quality strategy, regulatory compliance, and continuous improvement across the manufacturing lifecycle.
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Quality Assurance Specialist
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No Deviation Pte. Ltd.
Singapore, S00, SG
20d
Establish, maintain, and continuously improve the Quality Management System (QMS) for a research laboratory and a new GMP facility in Singapore, ensuring compliance with international standards like FDA CMC/HSA, GLP/GMP, GxP, ISO 9001, and ISO 17025.
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Spécialiste de la conformité réglementaire
Gsknch
Saint Laurent Montreal, CA
20d
Support regulatory submissions, post-approval change controls, and manufacturing transfer dossiers for a liquid/solid/semi-solid pharmaceutical manufacturing site.
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QA Manager & Responsible Person
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DHL Supply Chain
Dublin, County Dublin, Ireland
20d
Oversee Pharmaceutical Quality Management System and ensure compliance with EU GDP, HPRA requirements, and Wholesale Distribution Authorisation.
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Site Director, Development Quality
AstraZeneca
Durham, North Carolina, United States of America
$142k–$213k
20d
Senior leadership role protecting patients and ensuring GMP standards in pharmaceutical development while enabling teams to deliver with pace and confidence.
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Quality Control Inspector II - Hartland, WI 2nd shift
Medline
Hartland, Wisconsin, US
$44k–$64k
20d
Oversees quality projects, ensures compliance with SOPs, and maintains product integrity at a distribution center by inspecting raw materials and finished goods, managing holds/releases, and performing recalls.
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Senior Specialist, QA Operations Investigations
Bristolmyerssquibb
Leiden – NL
20d
Review and approve manufacturing and laboratory investigations, CAPAs, and effectiveness checks to ensure product quality and regulatory compliance.
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Senior Quality Assurance Specialist
↗
Valtera Group Ltd
Vienna, Austria
20d
Review batch documentation, prepare GMP batch certification and GDP release, and design/implement lean Product Quality Review processes across a full pharmaceutical product portfolio.
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Senior Specialist, QA Operations Investigations
Bms
Leiden – NL
20d
Review and approve manufacturing and laboratory investigations, CAPAs, and effectiveness checks to ensure product quality and regulatory compliance.
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Mitarbeiter*in QA-Oversight Qualifizierung, Wartung, Kalibrierung, und DataIntegrity
Bayer
Weimar,Thuringia,Germany
20d
Ensuring compliance with GxP regulations for equipment, room, and computer system qualifications, calibrations, and maintenance through QA oversight and document approval.
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Quality Specialist II - Complaints
Thermofisher
Greenville, North Carolina, USA
20d
Ensure compliance with GMP standards, FDA regulations, and international quality requirements while supporting manufacturing operations and maintaining quality management systems.
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Site Quality Head, Morrisville (Director)
Novartis
Morrisville, US
$168k–$312k
20d
Lead the independent site Quality organization for a new Small Molecule manufacturing site through ramp-up and commercialization, ensuring regulatory compliance and operational excellence.
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Višja Odgovorna oseba za sproščanje zdravil na trg (m/ž/d)
Novartis
Ljubljana, SI
€47k–€87k
20d
Senior Responsible Person for Batch Release ensuring compliance with EU GMP and legal requirements for aseptic pharmaceutical manufacturing.
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Site Director, Development Quality
AstraZeneca
US - Durham - NC
$142k–$213k
20d
Senior leadership role protecting patients and ensuring GMP standards in pharmaceutical development while enabling teams to deliver with pace and confidence.
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Quality specialist III
Thermofisher
Greenville, North Carolina, USA
20d
Drive quality execution across sterile operations including manufacturing, filling, packaging, and inspection for commercial and product development services.
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Qualified Person
Gsknch
Ireland - Dungarvan
€67k–€92k
20d
Certify and release medicinal products ensuring compliance with EU GMP, Marketing Authorisations, and regulatory standards.
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Specialist Quality Assurance (Technical Support)
Amgen
Singapore Manufacturing - Tuas
20d
Provide quality oversight and leadership for quality systems execution and operations support in non-direct manufacturing areas (Facilities & Engineering, QC, Technology, Process Development, Validation) for Biologics and Synthetic Manufacturing plants.
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QA Officer - Junior, Medior & Senior
Lonza
NL - Geleen
€41k–€58k
20d
Ensure life-changing medicines are manufactured to the highest quality standards by supporting GMP operations and collaborating with manufacturing teams.
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Pharmacien Qualité Produit H/F
Ipsen
Signes, Toulon
20d
Product Quality Pharmacist responsible for batch release certification, quality investigations, and operational quality oversight for internal production, external suppliers, and outsourced manufacturing.
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PHARMACIEN Assurance Qualité Délégué sur site PARIS-IDF F/H
AD HOMINEM INTERNATIONAL
Bobigny, Seine-Saint-Denis
21d
Ensure compliance with pharmaceutical regulations, manage quality systems (SMQ), and oversee pharmaceutical operations at the site.
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Responsable Assurance Qualité Opérationnelle F/H
CENTRE LAB PHARMA
Guéret, Creuse
€36k
21d
Ensure on-site application of current rules and standards (GMP, Pharmacopoeia, ISO norms) to enable safe market launch of pharmaceutical products.
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Ingénieur assurance qualité opérationnelle F/H
AMARYLYS
Nord, Hauts-De-France
21d
Release of pharmaceutical batches by reviewing manufacturing, control, and packaging dossiers to ensure compliance with GMP specifications.
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Senior Material Handler
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Thermo Fisher Scientific
Buenos Aires, B, AR
21d
Senior analyst supporting clinical trial operations through quality investigations, procurement coordination, and warehouse coverage.
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Quality Analyst I
↗
Mark Cuban Cost Plus Drug Company
Dallas, TX, US
21d
Ensures product quality and regulatory compliance through analytical testing, documentation review, and process oversight in pharmaceutical manufacturing.
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Biologe (m/w/d)
Daiichi Sankyo Europe GmbH
Pfaffenhofen an der Ilm, BAYERN
21d
Key User responsible for the technical support, maintenance, and development of SAP Quality Management (QM) processes within a regulated pharmaceutical environment.
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Associate Director, RCQA APAC ex-India
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Fortrea Singapore Pte. Ltd.
Outram, S00, SG
21d
Strategic regional RC&QA solutions partner providing line management, day-to-day quality leadership, and regulatory compliance advice across APAC ex-India for clinical trials.
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Vendor Quality Senior Manager (Contract)
↗
Vertex Pharmaceuticals
Remote
$156k
21d
Proactively assess vendor risk in GxP areas and translate assessments into insights, recommendations, and actions to demonstrate appropriate oversight of third parties.
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Quality Assurance Associate
↗
Nutrasource
Guelph, ON, CA
$50k–$60k
21d
Conduct QA audits, provide GCP/GLP oversight, and maintain quality systems to ensure GxP compliance and regulatory adherence across CRO, clinical trials, and analytics activities.
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Sr. QA Operations Specialist – Visual Inspection
Pciservices
Bedford, NH, USA
21d
Ensuring quality and compliance for visual inspection, final product sampling, packaging, storage, and shipment of pharmaceutical products.
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Spécialiste Assurance Qualité Système Compliance - Performance & Gouvernance H/F
Kenvue
Europe/Middle East/Africa, France, Normandy, Val-de-Reuil
21d
Piloter la gouvernance, la performance et l'amélioration continue de quatre processus qualité clés (Change Control, Gestion documentaire, Formation, Archivage) pour un site fabricant pharmaceutique.
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Manager, CMC Quality, Pulmovant
↗
Remote, US
21d
Ensure quality oversight of vendors for drug substance, drug product, and finished product manufacturing, testing, release, and distribution in compliance with cGMPs for a clinical-stage biotech's pulmonary hypertension treatment.
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QA Specialist _ Supplier Quality
Myhrabc
Columbus, OH, US
21d
Ensuring quality and compliance of materials and services from suppliers for American Health Packaging through evaluations, audits, and issue resolution.
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Senior Specialist, Field Quality QA Operations
Bms
Devens - MA - US
$90k–$108k
21d
Ensuring GMP compliance and quality oversight in day-to-day manufacturing operations through batch record review, on-floor inspections, and deviation resolution.
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Senior Specialist, Field Quality QA Operations
Bristolmyerssquibb
Devens - MA - US
$90k–$108k
21d
Ensuring GMP compliance and quality oversight in day-to-day pharmaceutical manufacturing operations by reviewing batch records and conducting floor inspections.
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