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Healthcare
› Pharma Manufacturing QA
Pharma Manufacturing QA
699 open positions
Quality Specialist I
Catalent
Kansas City, MO, US
1d
Quality Specialist supporting clinical trial projects by ensuring compliance with regulatory requirements, GMP, and SOPs through documentation, inspection, and release activities.
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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 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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Quality Manager | Pharmaceutical Warehouse Operations
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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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Młodszy Specjalista / Młodsza Specjalistka Zapewnienia Jakości w Obszarze API
Polpharma S.A.
Starogard Gdański, pomorskie
3d
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
3d
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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Quality Control Project Manager
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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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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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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
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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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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Compliance Auditor x3
Lonza
Remote
4d
Design, plan, and execute high-impact corporate cGMP audits across global manufacturing sites to safeguard license to operate and mitigate quality risks.
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Compliance Manager
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Thermo Fisher Scientific
En remoto, ES
4d
Assess, manage, and report on audits to ensure compliance with quality assurance processes, regulatory guidelines, and client obligations for clinical development programs.
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Quality Assurance Director
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Lampire Biological Laboratories
Pipersville, PA, US
4d
Lead quality compliance and drive quality improvement for a biotech life science company providing biological reagents to pharmaceutical, diagnostic, and biotech industries.
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Quality Assurance Officer
Thermofisher
Auckland, New Zealand
4d
Ensure consistent execution of quality standards and regulatory compliance in a GMP environment to enable customer breakthrough discoveries.
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Quality Management Internship (Summer 2027)
Cardinalhealth
OH-Dublin-Cardinal Place, US
$0k–$0k
4d
Support quality and regulatory affairs policies governing distribution through administrative tasks, compliance research, and risk identification.
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UK Affiliate Quality Director & Responsible Person (RP/RPi)
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Genmab
London, ENG, GB
$92k–$138k
4d
Establish and maintain the UK affiliate Quality Management System and ensure compliance with UK Good Distribution Practice (GDP) and MHRA requirements while acting as the statutory Responsible Person (RP/RPi).
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QA Officer (Systems)
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Newcastle, ENG, GB
4d
Maintain site supplier assurance program, internal/external audit programs, and vendor qualification documentation.
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Manager, Quality Assurance
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Gilead Sciences
Foster City, CA, US
$136k–$136k
4d
Ensures compliance with quality objectives and regulatory requirements by supervising QA personnel, managing processes, and reviewing manufacturing data.
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QA Operations Supervisor
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American Regent
New Albany, OH, US
4d
Leading QA Operations activities at a sterile manufacturing site, supervising technicians, investigating deviations, and ensuring compliance with cGMP standards.
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Quality Assurance Supervisor
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Fagron
Canton, MA, US
4d
Lead quality assurance activities for cGMP manufacturing, documentation, and product disposition to ensure compliance and proper controls in compounded product operations.
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Director, Quality Operations
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Kindeva Drug Delivery
Los Angeles, CA, US
4d
Lead Quality Assurance and Quality Systems functions for a contract manufacturing environment producing transdermal and inhalation combination drug products.
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Specjalista/-ka ds. Jakości
Vwr
Gliwice, POL, PL
4d
Supporting quality systems, managing quality documentation, and participating in continuous improvement initiatives within a regulated environment.
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Quality Assurance Associate II or Engineer I
↗
University of Colorado
Aurora, CO, US
$63k–$63k
4d
Support batch release, material release, and equipment qualification activities for GMP and non-GMP cell therapy and biologic batches in an academic Phase I cGMP contract manufacturing facility.
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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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Product Lifecycle Supervisor
Gsknch
Aprilia Nettunense, IT
$32k–$44k
4d
Oversees the product lifecycle for a manufacturing site, managing Periodic Product Reviews (PPR), change controls, stability programs, and complaints to ensure regulatory compliance.
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Senior Manager Corporate Quality Compliance
Amgen
United States - Remote
$138k–$138k
4d
Execute Global Quality Compliance tasks and projects to achieve corporate and departmental goals, including leading audits of the Quality Management System, sites, and suppliers.
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Associate Director, QMS & Compliance
Catalent
Swindon, United Kingdom
4d
Lead the Quality Management System (QMS) and ensure regulatory compliance for a pharmaceutical manufacturing and analytical lab facility.
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Investigation Specialist I
Pfizer
United States - Massachusetts - Andover
$60k–$60k
4d
Lead GMP investigations for manufacturing deviations, product quality excursions, and compliance events to ensure patient access to medicines.
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German Affiliate Quality Director & Responsible Person (RP)
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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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Compliance Manager
Thermofisher
Remote, Spain
4d
Assess, manage, and report on audits to ensure compliance with quality assurance processes, regulatory guidelines, and client obligations for clinical development programs.
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Senior QA Specialist
Thermofisher
Zaventem, Belgium
4d
Lead quality assurance efforts to maintain and enhance the quality and compliance of clinical research programs, managing audits, investigations, and quality improvement initiatives.
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Quality Customer Interface SEA Manager
Lonza
TH - Bangkok
4d
Primary Quality interface between Commercial teams and customers across Southeast Asia and Australia/New Zealand, ensuring customer requirements, inquiries, complaints, and escalations are resolved compliantly while driving quality improvements.
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Quality Associate
PharmaPOD
Prestons, New South Wales
4d
Ensuring the safety and quality of manufactured medicine components pre- and post-production, focusing on release for supply activities.
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QA Manager (Responsible Person Lead) - Team of 3
AbbVie
Zwolle, Overijssel
4d
Manage and lead Responsible Persons (RP) and Quality Assurance teams for VLOG entities, ensuring compliance with AbbVie and Regulatory Agency standards across the supply chain.
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Senior Quality Risk Management Engineer
AbbVie
North Chicago, IL, us
4d
Senior Quality Risk Management Engineer leading site-level QRM program deployment, risk assessments (FMEAs), and compliance with global QRM processes and cGMP regulations.
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Młodszy Specjalista / Młodsza Specjalistka ds. Zapewnienia Jakości
Polpharma S.A.
Starogard Gdański, pomorskie
5d
Supporting GMP compliance and quality processes for the API Business Unit, including batch verification, change control, and audit preparation.
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