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Healthcare
› Pharma Manufacturing QA
Pharma Manufacturing QA
1,628 open positions
Quality Assurance Project Manager
Lonza
US - Houston, TX
14d
Lead and manage Quality Assurance projects for onboarding, technology transfer, and implementation of Cell Therapy and Biologics clients in a GMP manufacturing environment.
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Quality Assurance Auditor 2
Iqvia
Austin, Texas, United States of America
$54k–$135k
14d
Conduct internal audits, oversee CAPA activities, and support regulatory inspections to ensure compliance with GxP requirements in a protein biomarkers laboratory.
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Site Quality & Compliance Lead and Responsible Pharmacist (East London)
Kenvue
Europe/Middle East/Africa, South Africa, West Cape, Cape Town
14d
Lead, manage, and implement site quality systems and plant quality in compliance with South African/Sub-Saharan Africa regulations and Kenvue standards while acting as the Responsible Pharmacist.
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Document & Training Specialist, Radioconjugate PQS
AstraZeneca
Hamilton, Ontario, Canada
14d
Administer controlled document management and learning management systems to ensure SOPs, training curricula, and records comply with GxP regulations and data integrity principles.
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Polytechnic Internship - QA Operations, Singapore (March 2027 to August 2027)
Gsk
Singapore - Tuas
14d
Support QA Operations in vaccine manufacturing through process reconciliation, batch record management, and quality improvement projects.
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Técnico Operacional M/T
↗
Unolab Manufacturing
Getafe, Community of Madrid, Spain
14d
Investigate and analyze deviations, out-of-specification (OOS) results, and complaints to identify root causes and implement corrective and preventive actions (CAPA) to ensure quality standards in a pharmaceutical manufacturing environment.
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Global Quality Assurance Auditor, Pharmacovigilance
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GE HealthCare
Saskatchewan, Canada
$102k–$153k
14d
Providing QA auditing and Global Compliance support to GMP manufacturing sites and Pharmacovigilance (PV) related functions within the Pharmaceutical Diagnostics business.
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Quality Assurance Manager
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Grupo Crit
Parets del Vallès, Catalonia, Spain
€40k
14d
Lead the Quality Assurance function for a veterinary pharmaceutical sterile manufacturing line, ensuring compliance with GMP standards and Annex 1 of the EU GMP Guidelines.
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Quality Compliance Lead
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WuXi XDC
Singapore, Singapore
14d
Leading site Quality Compliance function to ensure GMP inspection readiness and regulatory compliance across quality systems and operations.
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QA Auditor II
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Thermo Fisher Scientific
Athlone, Ireland
14d
Conduct routine client, internal, and GxP audits to ensure compliance and excellence in clinical auditing processes.
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Executive - Quality Assurance (QA-006)
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St Logistics
14d
Execute quality control activities for incoming, in-process, and outgoing products/shipments; manage customer relationships and complaints; support internal and external quality audits; and maintain documentation systems.
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QC Systems Administrator - Empower
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Catalyx
Cork, County Cork, Ireland
14d
Provide day-to-day system support for Empower, a quality management system, acting as a key point of contact for the customer site in Cork.
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Quality and Compliance Administrator
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Perrigo Company PLC
Dublin, County Dublin, Ireland
14d
Support the QA team in maintaining and enhancing the Quality Management System for Perrigo Supply Chain International DAC, ensuring compliance with Marketing Authorisation Holder, Manufacturing Importation Authorisation, Wholesale Distribution Authorisation…
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Executive - Quality Assurance (QA-006)
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St Logistics
Tuas, West Region, Singapore
14d
Execute quality control activities for incoming, in-process, and outgoing products/shipments, manage customer relationships, and support continuous improvement in a regulated environment.
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Qualified Person
Viatris
Baldoyle, Dublin, Ireland
14d
Certify medicinal products in accordance with EU GMP and marketing authorization requirements, ensuring product release and quality system effectiveness.
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Quality Manager
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Sanisure
Stapleford, England, UK
14d
Lead the management and continuous improvement of Plant Quality Systems, including CAPA, customer specification management, internal audits, and testing/inspection processes for single-use products in biological drug production.
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Associate Director Quality Management
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Iqvia
Madrid, Community of Madrid, Spain
14d
Lead quality improvement initiatives, risk-based quality management, and GCP compliance for clinical trial delivery across assigned business units.
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QA Graduate
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Eli Lilly and Company
Kinsale, Ireland
€49k
14d
A 24-month graduate programme for recent MSc/PhD graduates to develop practical Quality Assurance experience in a regulated manufacturing environment.
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Quality Assurance Administrator
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Galderma
Uppsala, Uppsala County, Sweden
14d
Administrative support for Quality Assurance processes, documentation control, and audit preparation in a regulated pharmaceutical environment.
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Quality Assurance Technician/Technicien de l'assurance qualité
Pg
GRTR TORONTO FULFILLMENT CTR, CA
14d
Ensure compliance with Health Canada requirements for imported regulated P&G products (drugs, natural health products, medical devices, food) and execute quality release processes.
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Associate Director Quality Management
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Iqvia
Remote
14d
Lead quality improvement initiatives, risk assessment, and GCP compliance for clinical trial delivery within assigned business units.
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Supply Operation Quality Associate
Pfizer
China - Shanghai - Shanghai
14d
Evaluate and review clinical and commercial drug batches to ensure quality and compliance with cGMP standards.
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Quality Assurance Specialist (Manufacturing / GMP)
↗
Laboratorios Rubió
Castellbisbal, Catalonia, Spain
14d
Ensuring regulatory compliance in a GMP environment and guaranteeing the correct functioning of the quality system regarding operations, training, documentation, incidents, and validations.
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Sr Compliance Specialist
Thermofisher
Ridgefield, New Jersey, USA
14d
Establishes and maintains quality systems for investigational new drugs, biologics, and medical devices to ensure compliance with regulatory and customer requirements.
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Team Leader, Quality Assurance
Thermofisher
Allentown, Pennsylvania, USA
14d
Lead the Quality Assurance team and oversee quality functions for clinical packaging operations, ensuring compliance with GMP and FDA regulations for pharmaceutical products.
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stage 4 à 6 mois documentation assurance qualité
Sanofi
Vitry-sur-Seine, FR
14d
Support the consistency, compliance, and maintenance of operational documentation (procedures, work instructions) for a biopharmaceutical site.
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Quality Assurance Administrator
Galderma
Uppsala, SE
14d
Administrative support for Quality Assurance processes, documentation control, and audit coordination in a regulated dermatology manufacturing environment.
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Quality Assurance Manager II
↗
DHL
Bethlehem, PA, US
$70k–$115k
14d
Manage and coordinate all aspects of quality assurance activities, regulatory compliance, and continuous improvement for a logistics site handling regulated hardware, equipment, and software systems.
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Manager, Quality Operations
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Labconnect, LLC
Remote
14d
Ensuring quality, timeliness, and regulatory compliance of operations within a central laboratory supporting clinical trials.
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External Quality Operations Manager
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Sobi - Swedish Orphan Biovitrum AB (publ)
Stockholm, Stockholm County, Sweden
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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QA Auditor III
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Thermo Fisher Scientific
Athlone, Ireland
14d
Leads complex internal and external audits to ensure compliance with quality assurance processes, global regulatory guidelines, and client contractual obligations.
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Senior Specialist, Quality
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Msd Ireland
Dundalk, County Louth, Ireland
14d
Provide independent quality oversight for Drug Substance and Drug Product manufacturing operations in a vaccines facility.
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Quality Assurance Specialist I
Catalent
Chelsea, MA, US
$70k–$85k
14d
Support Manufacturing Investigations and Corrective and Preventive Actions (CAPA) to ensure compliance and quality in GMP pharmaceutical manufacturing.
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QA Officer
Pciservices
Tredegar, UK
14d
Operational Quality Assurance Officer ensuring GMP compliance, batch release, and production oversight across manufacturing and packaging sites.
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Product Manager-Annual Product Reviews
Catalent
Winchester, KY, US
14d
Managing the Annual Product Review program to verify process consistency, assess trends, and ensure regulatory compliance for pharmaceutical manufacturing.
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Sachbearbeiter QA Systems (m/w/d) Pharma
expertum GmbH
Dessau-Roßlau, SACHSEN_ANHALT
14d
Administration of an electronic document management system (SmartSolve) for GMP-relevant documents, SOPs, and training materials within a pharmaceutical company.
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Manager of Non-Conformance - Root Cause Analysis/Deviations
Bristolmyerssquibb
Indianapolis - RayzeBio - IN, US
14d
Lead the site's deviation and non-conformance management program, driving rigorous root cause analysis (RCA) and corrective/preventive actions (CAPA) to ensure regulatory compliance and product quality.
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Senior Manager, QA Shopfloor Lead
Bms
Leiden – NL
14d
Senior Manager leading the QA Shopfloor program to ensure GMP compliance, real-time batch record review, and quality oversight of manufacturing operations at a Cell Therapy facility.
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Manager of Non-Conformance - Root Cause Analysis/Deviations
Bms
Indianapolis - RayzeBio - IN
14d
Lead the site's deviation and non-conformance management program, driving rigorous root cause analysis (RCA) and corrective/preventive action (CAPA) to ensure regulatory compliance and product quality.
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Quality Assurance Technician
↗
Grupo Medinfar
Amadora, Lisbon, Portugal
14d
Maintain and improve the Quality Management System, ensure regulatory compliance, and manage quality-related processes for pharmaceutical products.
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Principal Product Quality Leader
Amgen
United States - Remote
14d
Lead product quality strategies for late-stage and commercial biologics, ensuring product health through GMP compliance, regulatory filings, and risk assessments.
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QA Operations Officer
Viatris
Baldoyle, Dublin, Ireland
14d
Ensure product quality in manufacturing by monitoring operations, reviewing batch records, and managing deviations and changes.
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Quality Assurance Technician
Galderma
Uppsala, SE
14d
Quality Assurance Technician supporting sterile biologics manufacturing by ensuring GMP compliance, process adherence, and documentation integrity on the production floor.
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Commercial Quality Lead & QP UK
Kenvue
Europe/Middle East/Africa, United Kingdom, Reading, Berkshire
14d
Act as the Qualified Person (QP) and Responsible Person backup for the UK market, ensuring batch certification of medicinal products and compliance with UK MIA, EU GMP, and local regulations.
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Quality Systems Specialist
Viatris
Baldoyle, Dublin, Ireland
14d
Develop and implement site Quality Systems to support the manufacture and release of Combination products, including SOPs, document control, change control, investigations, CAPA, internal auditing, Vendor qualification & management, material and batch…
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Supervisor, Quality Assurance
Catalent
Winchester, KY, US
14d
Lead the Quality Assurance function to ensure compliance with Quality Systems, Finished Product Batch Release, and Change Control in a large-scale oral solid dose manufacturing facility.
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Dyrektor/ka ds. Jakości
Grupa Neuca
Poznań, wielkopolskie
14d
Overseeing the Quality Assurance system for a pharmaceutical distribution and production group, ensuring compliance with GMP, GDP, ISO, HACCP, and MDR regulations.
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Quality Senior Manager
AbbVie
North Chicago, IL, us
14d
Lead the Quality function for AbbVie's distribution and logistics, overseeing quality systems for owned warehouses, 3PL networks, and suppliers to ensure compliance and operational efficiency.
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Młodszy Specjalista / Młodsza Specjalistka ds. Zapewnienia Jakości
Polpharma S.A.
Nowa Dęba, podkarpackie
15d
Leading and participating in investigations of quality deviations and non-conformities in the manufacturing process of medicinal products.
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Senior Manager Quality Assurance (m/w/d)
Wasserburger Arzneimittelwerk GmbH
Wasserburg am Inn
15d
Leading and optimizing Quality Assurance operations, compliance, and team management in a sterile pharmaceutical manufacturing environment.
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