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Healthcare
› Pharma Manufacturing QA
Pharma Manufacturing QA
681 open positions
QA Release Analyst
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Ferring Pharmaceuticals, Inc.
Buenos Aires, B, AR
today
Reviewing and issuing API batch records, managing quality assurance documentation, and participating in internal audits for a pharmaceutical production plant.
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Responsable Qualité Opérationnelle
Nemera
Le Tréport, Normandy, fr
1d
Ensure product and operational compliance while driving continuous quality improvement at an industrial manufacturing site.
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Quality Assurance Manager*in (m/w/d) Operations
Lgc-Group
Berlin, BE, de
1d
Design and develop a GMP-compliant Quality Management System (QMS) for a new Life Science operations site, ensuring regulatory compliance and operational quality.
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Supervisor II, Quality Assurance (OSD) (3rd shift)
AbbVie
Barceloneta, Barceloneta, pr
1d
Oversees Quality Assurance operations on the manufacturing shop floor, ensuring GMP compliance, product release, and regulatory adherence for pharmaceutical products.
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Spécialiste AQ - Site Exploitant, France (CDD 8 mois)
AbbVie
Boulogne-Billancourt, fr
1d
Maintaining and improving the quality system for pharmaceuticals, medical devices, cosmetics, and aesthetic products at the operating site.
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Director Quality Science & Technology
Agilent
Canada-Prince Edward Island-Charlottetown
$131k–$131k
1d
Senior quality executive accountable for portfolio-level quality strategy, regulatory risk governance, and lifecycle readiness for biological drug substances, reagents, and complex chemistry molecules.
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Quality Assurance Specialist Nights
↗
Sanofi
Toronto, ON, CA
1d
Guardian of patient safety and product excellence through rigorous GMP record review, batch release activities, and shopfloor oversight to mitigate quality risks.
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QA Specialist
Sanofi
Le Trait, FR
$42k–$42k
1d
On-site Quality Assurance Specialist ensuring production compliance with regulatory requirements and GMP standards, resolving quality issues in real-time, and managing deviations and CAPAs.
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QA Specialist II - Doc Control
Pciservices
Bedford, NH, USA
1d
Manage, coordinate, and maintain cGMP documentation, procedures, and records to ensure controlled copies are reviewed, approved, issued, distributed, and archived within a biopharma quality management system.
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Quality Assurance Specialist Nights
Sanofi
Toronto, ON, CA
$76k–$110k
1d
Guardian of patient safety and product excellence through rigorous GMP record review, batch release activities, and shopfloor oversight to ensure regulatory compliance.
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Document Control Specialist
Gsknch
USA - New York - Oak Hill
1d
Manage document control applications and quality system activities to ensure product and process compliance with regulatory agencies and company standards.
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Sr Analyst, QA Assurance
↗
Baxter
São Paulo, SP, BR
1d
Investigate product failures, market complaints, and recalls to ensure patient safety and product quality within the pharmaceutical manufacturing lifecycle.
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Associate Manager-Investigation
Pfizer
India - Vizag
1d
Investigate quality issues, deviations, and out-of-specification results within manufacturing and quality laboratories to identify root causes and suggest corrective actions.
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QA Operations Expert (m/f/d)
↗
Novartis
T, AT
$67k–$105k
1d
Ensure quality and compliance of Drug Product manufacturing through hands-on oversight, batch release, and investigation management.
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Sr Analyst, QA Assurance
Baxter
São Paulo, BR
1d
Lead investigations into product failures, market complaints, and recalls; ensure compliance with global quality metrics; coordinate corrective and preventive actions to prevent recurrence.
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QA Operations Expert (m/f/d)
Novartis
Schaftenau, AT
$67k–$105k
1d
Provide hands-on quality oversight for Drug Product manufacturing, ensuring compliance with regulatory standards and GMP to safeguard patient safety.
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Executive Director, Quality Assurance
Msd
USA - New Jersey - Rahway
$210k–$210k
1d
Strategic oversight and direction for an enterprise-level transformation program to transform QC testing, analytical digitization, lab automation, and QMS systems within a GMP laboratory.
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QA/QMS Senior Specialist — Deviations & Investigations
Nivagen Pharmaceuticals
Sacramento, CA 95834
$80k–$80k
1d
Lead deviation management and root cause analysis for sterile GMP manufacturing operations to ensure regulatory compliance and product quality.
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Temp - QA Specialist
Regeneron
Limerick, IE
1d
Providing QA oversight and support for manufacturing operations, serving as the primary quality representative within production areas.
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Manager, Audits & Inspections - Quality Systems & Compliance
Thermofisher
Greenville, North Carolina, USA
1d
Lead quality oversight for client audits and regulatory inspections, ensuring compliance with FDA, EMA, and ISO standards in the pharmaceutical/medical device sector.
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Manager, Analytical Quality Assurance
Bristolmyerssquibb
New Brunswick - NJ - US
$93k–$93k
1d
Provide QA review and approval of technical documents and Quality Management System (QMS) records for Commercial GMP analytical methods for biologics and small molecules drug substances and drug products.
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VP, Quality Operations (Ireland or U.S. based)
↗
Zoetis
Parsippany-Troy Hills, NJ, US
1d
Ensure reliable supply of high-quality animal health products through a robust, compliant Quality Management System across BioPharmaceuticals and BioVaccines internal manufacturing operations.
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Manager, Clinical Program Documentation Control and Audit Readiness
Biibhr
Warsaw, Poland
$166k–$166k
1d
Manage clinical procurement documentation control, audit readiness, and evidence retrieval for CPSC activities to ensure compliance with regulatory inspections and quality reviews.
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VP, Quality Operations (Ireland or U.S. based)
↗
Zoetis
Parsippany-Troy Hills, NJ, US
1d
Ensures reliable supply of high-quality BioPharmaceuticals (mAbs) and BioVaccines through a robust, compliant Quality Management System across global internal manufacturing operations.
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Director/Senior Director, Quality Assurance
↗
Berkeley, CA, US
1d
Build and lead the Quality Assurance function for an early-stage biotechnology company developing in vivo genome editing cancer immunotherapies, ensuring GMP readiness and regulatory compliance for clinical supply.
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Quality Assurance Specialist - Cincinnati, OH
↗
Siemens Healthineers
Cincinnati, OH, US
$89k–$89k
1d
Provide quality oversight for a US-based site manufacturing and distributing radioactive sterile injectables (PET) per 21 CFR Part 212 and USP 825.
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Quality Manager | Pharmaceutical Warehouse Operations
↗
DHL
Cuautitlán Izcalli, MEX, MX
2d
Lead and ensure the execution of the Quality Management System (QMS) for pharmaceutical warehouse operations, guaranteeing compliance with regulatory requirements, Good Distribution Practices (GDP), and customer standards.
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Quality Technician I
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DHL
Arlington, TX, US
2d
Lead and support the Quality Assurance team to ensure compliance with governmental regulations, customer requirements, and internal QA policies through audits, training, and process improvement.
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Młodszy Specjalista / Młodsza Specjalistka Zapewnienia Jakości w Obszarze API
Polpharma S.A.
Starogard Gdański, pomorskie
2d
Ensuring GMP compliance and managing quality processes for API manufacturing in a CDMO environment.
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Pharma Manufacturing QA Site Supervisor (Must have API Pharma Exp/ Strong in QA Site Work) Up 12K HJC
Recruit Express Pte Ltd
Singapore
2d
Lead on-site quality assurance activities in manufacturing, packaging, and warehouse areas to ensure GMP compliance and manage material release and cleaning validation.
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Officer, QA Doc Cell
Amneal Pharmaceuticals
Ahmedabad, Gujarat
3d
Supports the quality assurance documentation cell in pharmaceutical manufacturing by defining quality activities, maintaining documentation infrastructure, and ensuring compliance with regulatory standards.
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Quality assurance officer H/F
Manpower
Genf
3d
Ensure compliance of industrial activities with quality requirements and Good Manufacturing Practices (GMP) while supporting operational teams in applying quality standards.
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GxP Compliance Experts
Personal Contact Group AG
Basel, Basel-Stadt
3d
SME for GxP and compliance topics, providing proactive consulting and system administration for Veeva QualityDocs, managing audits, deviations, CAPAs, changes, and quality KPIs for Life Sciences companies.
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Manager QA - EPD Quality Systems
Abbott
Mumbai, Maharashtra
3d
Manage Quality Systems initiatives and support process owners for Third-Party Manufacturer (TPM) and Supplier Quality Management to ensure safe, effective, and compliant product supply.
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Deputy Responsible Pharmacist
Afrizan People Intelligence
Cape Town City Centre, Cape Town Region
3d
Senior-level pharmacist ensuring regulatory compliance and quality standards in pharmaceutical warehousing and distribution.
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Head of Quality Assurance - Torrance
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Polypeptide Us
Torrance, CA, US
$160k–$160k
3d
Lead site Quality Assurance activities ensuring compliance with FDA, EMA, and cGMP regulations for peptide-based therapy development and manufacturing.
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Quality Control Project Manager
↗
Argonaut Manufacturing Services
Carlsbad, CA, US
$117k–$117k
3d
Lead and coordinate end-to-end Quality Control projects and programs for pharmaceutical and biopharmaceutical manufacturing, ensuring alignment with regulatory requirements, customer expectations, and business objectives.
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Regional Healthcare Quality Manager
Expeditors
Bellevue, WA, us
$85k–$85k
3d
Ensure regulatory compliance and quality standards for healthcare logistics operations, including GDP/GMP adherence, audit support, and risk management for pharmaceutical and medical device shipments.
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Quality Expert, Data Analytics and Statistical Support
Lonza
India
3d
Ensure consistency and compliance of manufacturing processes by generating control charts for Periodic Quality Review (PQR) and Continued Process Verification (CPV) reports.
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Senior Manager, QA Documentation
Amneal
Hyderabad, Telangana
3d
Ensure compliance with regulatory guidelines and standard operating procedures for QA functions in pharmaceutical manufacturing.
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Analista de Garantia da Qualidade Pleno
Dr Reddy's Laboratories Limited
Brasil
3d
Ensures compliance of Quality Assurance processes with Good Practices (BPx), regulatory requirements, and internal procedures by reviewing documentation, analytical data, and product releases.
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Analista de Garantia da Qualidade Pleno
Dr-Reddy-S-Laboratories-Limited
São Paulo, SP, br
4d
Ensures compliance of Quality Assurance processes with Good Practices (BPx), regulatory requirements, and internal procedures by reviewing documentation, analytical data, and product releases.
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Quality Assurance Engineer (Temporary 12 months) Visa Required
AbbVie
Heredia, Heredia Province, cr
4d
Manufacturing Quality Assurance functions including deviation resolution, product impact analysis, CAPA, SOP approval, calibration oversight, and cGMP compliance.
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NPI QA Specialist - 12 month FTC
AbbVie
Dublin, County Dublin, ie
4d
Ensuring new product integration and transfers meet regulatory requirements and AbbVie quality policies from development through commercialization.
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QA Compliance Specialist - 12 month contract
AbbVie
Sligo, ie
4d
Ensuring new products transferred to AbbVie Sligo are manufactured in accordance with regulatory requirements and company procedures.
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Kierownik / Kierowniczka jakości
POPŁAWSKA GROUP Spółka Jawna
Wrocław, dolnośląskie
4d
Leading the Quality Department (QC, QA, Documentation) for a cosmetics manufacturer, ensuring compliance with GMP and managing product registration.
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Senior QA Compliance & Continuous Improvement Lead
Lhh
Provincia di Frosinone, Lazio
$0k–$0k
4d
Senior Quality Assurance leader responsible for promoting quality compliance, inspection readiness, and continuous improvement initiatives within a pharmaceutical manufacturing site.
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Primary Quality Shopfloor Expert
Adecco Italia
Provincia di Siena, Toscana
$32k–$32k
4d
Ensure GMP compliance and operational procedures on the shopfloor, manage initial quality issues, and oversee critical activities and documentation in a pharmaceutical setting.
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Manager, Quality Assurance
Gilead
United States - California - Foster City
$136k–$136k
4d
Ensures compliance with quality objectives and regulatory requirements by supervising QA personnel, managing processes, and conducting audits in a GMP/GLP environment.
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German Affiliate Quality Director & Responsible Person (RP)
↗
Genmab
München, BY, DE
$98k–$146k
4d
Establish and maintain the German affiliate's Quality Management System and ensure compliance with EU GDP and German pharmaceutical legislation as the statutory Responsible Person.
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