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Healthcare
› Pharma Manufacturing QA
Pharma Manufacturing QA
1,629 open positions
Sr Supervisor, Quality
Baxter
Hayward, California, US
$88k–$121k
16d
Lead QA Inspectors and oversee inspection, review, and release of materials and products in a cGMP-regulated manufacturing environment.
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QPIC
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Gfl Environmental Inc.
Etobicoke, Ontario, Canada
16d
Oversee AQPICs and Ops Analysts for pharmaceutical returns and waste processing, ensuring site compliance and managing customer audits.
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Change Control Manager
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Grifols
Mississauga, Ontario, Canada
16d
Manage and supervise change controls for processes, systems, technology, work roles, and organizational structures to evaluate impact on product licenses approved by Health Competent Authorities.
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Pharmaceutical Quality Director – Mexico
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Hunters Group
16d
Lead quality assurance, quality control, and regulatory compliance for a major pharmaceutical manufacturing operation in Mexico.
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Assoc Director, Quality Assurance
Gilead
United States - California - Foster City
$182k–$236k
16d
Provide Quality Assurance oversight of GMP Manufacturing and QC testing operations, ensuring compliance with cGMP and regulatory standards for biologics.
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2027 Intern - QA, QMS
Catalent
Madison, WI, US
16d
Intern supporting Quality Systems projects, process improvements, and automation initiatives in a biologics manufacturing facility.
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Manager, Quality Assurance – Western U.S. (West of the Mississippi) & Florida
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Gilead Sciences
Remote, US
$124k–$160k
16d
Manage qualification, monitoring, and compliance for apheresis collection and treatment centers supporting Kite's CAR-T cell therapy products.
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Lead Specialist, Quality Control
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Lonza
Tuas, West Region, Singapore
16d
Lead quality control protocols, stability studies, and investigations to ensure pharmaceutical manufacturing meets highest quality and safety standards.
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Supplier Quality Expert / Auditor
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Grünenthal Group
Lisbon, Lisbon, Portugal
16d
Lead quality oversight of supplier products and supply chains, ensuring compliance with GMP and regulatory requirements while managing audits and supplier performance.
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Manager, Quality Assurance – Western U.S. (West of the Mississippi) & Florida
Gilead
United States – Remote
$124k–$160k
16d
Manage qualification, monitoring, and compliance for apheresis collection and treatment centers supporting Kite's CAR-T cell therapy products.
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Quality & Improvement Manager
Vwr
Cambridge, GBR, GB
16d
Lead Quality Management Systems (QMS) and drive continuous improvement initiatives to ensure compliance, safety, and operational excellence in a pharmaceutical R&D environment.
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Head of Patient-Facing Quality Assurance
Csl
Seqirus UK - Maidenhead
16d
Lead an integrated Quality Assurance organization covering Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP) to ensure participant safety, data integrity, and regulatory compliance in clinical trials and post-market monitoring.
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Sr. Manager Quality Audit and Compliance
Acadia Pharmaceuticals
Princeton, New Jersey, United States; San Diego, California, United States
$138k–$172k
16d
Leading internal and external GMP audit activities and maintaining robust quality systems for a pharmaceutical company's growing portfolio.
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Manufacturing Quality Specialist (2nd Shift)
Eurofins
Louisville, KY, us
16d
Ensures quality and compliance of oligonucleotide products throughout the manufacturing process per ISO 13485, ISO 9001, and 21 CFR 820.
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Senior Regulatory Pharmacist
Zuellig Pharma
Singapore
17d
Lead regulatory compliance, product registration, and pharmacovigilance activities to ensure the safe distribution of healthcare products in Singapore.
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Director, Quality Risk Management (QRM), Global QMS, R&D & PV QA
DAIICHI SANKYO SINGAPORE PTE. LTD.
Singapore
17d
Establish, govern, and advance a global Quality Risk Management (QRM) framework across R&D, Pharmacovigilance, and Medical Affairs to ensure proactive identification, assessment, and control of quality risks in alignment with ICH Q9 (R1) and GxP regulations.
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Quality Assurance Specialist (Pharmaceutical Logistics)
Kuehne+Nagel
Singapore
17d
Ensuring quality standards and regulatory compliance across pharmaceutical warehousing and logistics operations from receipt to delivery.
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Quality Control Specialist II (m/f/d)
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Novartis
Kundl, Tyrol, Austria
€61k–€96k
17d
Oversee production and testing activities, ensuring compliance with Good Manufacturing Practice and quality standards in a pharmaceutical/biotechnology setting.
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Senior QA Manager ESO Biosimilars, LM
Sandoz
India
17d
Ensures manufacturing, testing, release, and distribution of biologics and sterile pharmaceutical products at external supplier sites comply with cGMP and regulatory requirements.
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Assistant Manager, QA Validation
Amneal
India
17d
Define and specify quality activities, processes, and standards for validation programs in compliance with regulatory requirements to ensure timely delivery of validated and compliant pharmaceutical products.
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Assistant Assurance Qualité F/H
CEBIPHAR
France
18d
Participate in maintaining the quality system for the Microbiology and Veterinary departments through audits, documentation management, and event tracking.
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Responsable Affaires Pharmaceutiques & PRI F/H
AMARYLYS
2ème Arrondissement, Paris
18d
Ensure pharmaceutical compliance for drug distribution, maintain quality systems, support pharmacovigilance, and manage quality complaints and batch recalls.
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Pharmacien Assurance Qualité & PRI F/H
AMARYLYS
1er-Arrondissement, Lyon
18d
Interim Quality Manager responsible for regulatory compliance and quality management system in a pharmaceutical manufacturing setting.
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Quality Assurance Manager
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Lifescience Logistics
Durham, NC, US
18d
Ensure compliance with FDA regulations and cGMP across 3PL operations, lead regulatory inspections, and oversee the Quality Management System including deviations, CAPA, and data integrity.
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Senior QA Specialist, CVRM
Roche
Holly Springs, US
$94k–$175k
18d
Provide Quality oversight for all manufacturing and warehouse operational activities, support functions, and directly collaborate with cross-functional partners to guarantee strict adherence to quality standards in a sterile drug product manufacturing…
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QA Auditor III
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Thermo Fisher Scientific
Remote
18d
Conduct and lead GCP audits, regulatory inspections, and site/vendor audits to ensure clinical trial compliance and quality standards.
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Principal QA Specialist (Multi-dose pens), CVRM
Roche
Holly Springs, US
$115k–$213k
18d
Principal QA Specialist ensuring end-to-end quality for cartridge filling, inspection, assembly, and packaging in a sterile drug product manufacturing facility.
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Principal QA Specialist (Assembly & Packaging), CVRM
Roche
Holly Springs, US
$115k–$213k
18d
Principal QA Specialist ensuring end-to-end quality for Assembly, Packaging, and Warehouse operations in a new drug manufacturing facility.
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Quality Operations Associate (2nd Shift)
Eurofins
Durham, NC, us
18d
Support product compliance activities within a warehouse by performing AQL sampling, inspecting hand-packaged materials, managing drug returns, and staging materials for production.
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Manager, QC
West Pharmaceutical Services
Jurong Town, West
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 pharmaceutical manufacturing environment.
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Quality Assurance Officer
DHL Supply Chain
New South Wales
19d
Lead quality assurance for warehouse operations in pharmaceutical or food industries, ensuring compliance with GMP and managing audits.
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Associate Director / Director, Quality Assurance
Arspharmaceuticalsoperationsinc
Corporate HQ
$206k
19d
Senior QA leader owning the Quality Management System for an outsourced manufacturing model, including document control, GMP training, and supplier/vendor audit programs.
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Specialist III – Quality Assurance, Systems
Catalent
Madison, WI, US
19d
Manage complex deviations, Out-of-Specification investigations, and Corrective and Preventive Actions (CAPAs) to ensure compliance and operational excellence in biologics manufacturing.
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Analista calidad | Sector farmaceutico
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DHL Supply Chain
Cuautitlán Izcalli, México, Mexico
$15k
19d
Quality Analyst responsible for product inspection, sampling, and documentation control within a pharmaceutical logistics environment.
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Senior Quality Systems Engineer/APQR Lead
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Tris Pharma Inc
Monmouth Junction, NJ, US
19d
Leads Annual Product Quality Reviews (APQRs) and statistical trending to ensure commercial pharmaceutical products meet safety, identity, strength, quality, and purity standards.
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Director of Quality Control (Montes Claros - MG)
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Novo
Montes Claros, MG, BR
19d
Lead Quality Control operations and a team of ~80 colleagues at a pharmaceutical manufacturing site to ensure medicines meet quality requirements and GMP standards.
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Quality Manager
Cycle Pharmaceuticals
Cambridge, UK
19d
Ensure quality and compliance across the pharmaceutical product lifecycle from development to commercial supply, overseeing external manufacturing partners and regulatory inspections.
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Quality Excellence Manager
Sanofi
Swiftwater, PA, US
$113k–$164k
19d
Drive operational excellence and product quality within pharmaceutical manufacturing by implementing continuous improvement initiatives and managing quality metrics.
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M&S-China EM&S Quality Regulatory Manager-Shanghai
Sanofi
Shanghai, CN
19d
Establish and maintain Quality Management Systems for contract manufacturing, manage local product regulatory compliance, and supervise production processes to ensure adherence to GMP and regulatory requirements.
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Quality Lab Supervisor - Night shift
Flextronics
USA, IL, Buffalo Grove
$65k–$90k
19d
Supervises and coordinates Quality Assurance Inspection activities, including quarantine, disposition of nonconforming goods, and ensuring policy/process compliance.
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Sachbearbeiter Qualitätsdokumentation (m/w/d), Neumarkt
BIONORICA SE
Neumarkt in der Oberpfalz, BAYERN
€46k–€53k
19d
Create specifications and analysis certificates for raw materials, packaging, and finished products; coordinate quality management processes in GMP-regulated pharmaceutical production.
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CAPA Leader
Gehc
Cork, IE
19d
Lead the Quality Management System by owning CAPA, deviation management, change control, and investigations to drive continuous improvement and compliance in a highly regulated environment.
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Sr QA Reviewer, Biologics Approval
Thermofisher
Foster City, California, USA
$85k–$94k
19d
Provide quality assurance lifecycle support for analytical testing activities in biologics, focusing on oversight of method transfers, qualifications, validations, investigations, and risk assessments conducted by external partners.
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Spvr Quality Control
Regeneron
RENSSELAER, US
$79k–$129k
19d
Supervise QC staff and oversee daily operations of Drug Product Packaging and Medical Device Components testing to support testing and release.
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Manager, QA, Data Integrity Program Manager
Lonza
CH - Visp
19d
Support the site's Data Integrity (DI) program at a biologics manufacturing site to ensure product quality, patient safety, and regulatory compliance.
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Manager, Quality Systems & Compliance - Deviation/CAPA/Complaints
Thermofisher
Greenville, North Carolina, USA
19d
Lead a team of quality professionals to oversee deviation, CAPA, and complaints management programs ensuring regulatory compliance and operational excellence in pharmaceutical and medical device operations.
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Sr Mgr SC & Logistics Global Compliance
Regeneron
RENSS - TEMPEL LN, US
$126k–$206k
19d
Lead and develop a global team managing compliance activities, investigations, change controls, and CAPA for Supply Chain and Logistics operations at IOPS sites globally.
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Qualified Person (QP) - Pharmaceutical Manufacturing
Airproducts
Lille, France
19d
Ensuring quality, safety, and compliance of medicinal gases manufactured at the Templemars site in France, including batch certification and release.
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Quality Control Specialist II (m/f/d)
Novartis
Schaftenau, AT
€61k–€96k
19d
Oversee production and testing activities, review and approve quality control data, and support investigations to ensure compliant pharmaceutical manufacturing.
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Director, CMC Quality
AbCellera
Vancouver
CA$180k–CA$220k
19d
Technical quality expert for antibody products during clinical development through post-commercialization, ensuring product quality, regulatory compliance, and lifecycle continuity.
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