Pharma Manufacturing QA
752 open positions
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Manager, Supplier & Internal Auditor VaxcyteRemote $151k–$151k8d Plan, execute, and manage supplier and internal audits to ensure compliance with global regulations and quality systems for a clinical-stage vaccine company.
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Quality Assurance Associate CatalentStrathroy, Canada $48k–$48k8d Support product release, coach operators on documentation, and ensure compliance with cGMP to prevent quality issues in softgel manufacturing.
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MQA Specialist II FreseniusglobalMelrose Park, IL, US $79k–$79k8d Performs routine audits of manufacturing areas to ensure product quality and SOP/GMP compliance at the Melrose Park Manufacturing Facility.
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QC Manager NeurocrineUS CA San Diego $120k–$120k8d Oversight of GMP analytical testing performed by contract sites and internal GMP analytical laboratory operations.
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QA Operations Specialist MsdIRL - Louth County - Dundalk 8d Provide direct quality support and oversight to manufacturing operations for vaccine production, ensuring compliance with GMP and documentation practices on the shop floor.
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QA Officer ThermofisherCovingham, Swindon, United Kingdom 8d Lead the site Product Quality Review (PQR) process and act as a Deviation Investigator for quality events in a GMP pharmaceutical manufacturing environment.
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Quality Compliance Support Expert GskHungary Gödöllő $8872k–$8872k8d Local Master Data Business Owner responsible for coordinating and supervising GMPM module SAP processes related to Quality, managing Method of Analysis (MoA) documents, SOPs, and supplier quality assessments.
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Commercial Quality Intern KenvueEurope/Middle East/Africa, Spain, Community of Madrid, Madrid 8d Maintain Quality Standards and Systems for the Spanish Consumer Health organization and support European cluster teams in optimizing processes.
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QA Compliance Auditor, Central Lab Services LabcorpShanghai China 8d Conduct internal, vendor, and sponsor audits; support regulatory and accreditation inspections (NMPA, CAP, ISO 15189); ensure regulatory compliance and quality assurance responsibilities are followed.
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Senior Director, GMP Quality↗ Generate BiomedicinesBoston, MA, US 8d Build and maintain fit-for-purpose GMP quality systems, provide independent oversight of CDMOs and contract labs, and ensure products/processes meet regulatory GxP requirements for biologics.
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Clinical Supply Associate (12 months fixed term/secondment) AstraZenecaPoland - Warsaw 8d Manage clinical material delivery, quality complaints, and supply chain processes to support drug development projects.
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GLP/GCLP Vendor Oversight and QA Lead (EU) CslSeqirus UK - Maidenhead 8d Lead quality oversight and governance for external partners (CROs, labs) supporting nonclinical GLP research to ensure data integrity and regulatory compliance.
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Quality Assurance Specialist III PrecisionmedicinegroupWinston Salem, NC $92k–$92k8d Provide on-site advanced-level hands-on support for GxP laboratory services and kitting production, managing document control, internal audits, and quality inspection/release of materials and products.
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R&D Senior Quality Manager (all gender) | Austria AltenRemote $48k–$48k8d Ensure quality oversight for complex R&D projects and global quality initiatives, acting as the key QA partner for cross-functional stakeholders.
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Quality Assurance Specialist (M/F) RoquetteStade, DE 9d Ensure compliance and operational excellence across food additive and pharmaceutical excipient manufacturing sites by driving quality culture and continuous improvement.
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Quality Specialist 3 - Quality Systems↗ Merck KgaaRockville, MD, US $71k–$106k9d Ensures compliance with cGMP, GLP, and regulatory requirements for Contract Testing Services by executing quality systems activities.
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Manager - External Supply Operation Quality PfizerSingapore - Mapletree Business City 9d Manage product quality and compliance for a portfolio of external contract manufacturers and suppliers to ensure on-time delivery of high-quality products in adherence to GMP/GDP regulations.
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Corporate Quality Assurance Manager↗ Prudential Overall SupplyIrvine, CA, US 9d Lead and advance the enterprise Quality Management System (QMS) across all laundry plants, ensuring ISO compliance and supporting cleanroom and life-science service offerings.
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Analista De Operacion Cedi FreseniusmedicalcareBenito Juarez, MX, MEX 9d Monitor quality processes, maintain documentation, and support audits to ensure compliance with quality standards and Good Storage and Distribution Practices.
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Senior Manager Quality Operations (m/f/d)↗ Fresenius KabiRemote $60k–$60k9d Ensure GMP compliance for drug substance, drug product, and combination products across development, tech transfer, analytical transfer, and commercialization phases.
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QA Associate - Laboratory - One Year Contract↗ Total Health Centre ( Reena Group)Mississauga, ON, CA $50k–$50k9d Ensure pharmaceutical quality assurance systems meet regulatory requirements through documentation management, equipment calibration, and OOS investigation.
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CHARGE.E QUALITE SYSTEMES ExpanscienceEpernon, France 9d Maintaining and improving industrial site quality systems in compliance with regulatory requirements and applicable standards.
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Quality Engineering, QA Expert, Commissioning & Qualification Audit and Inspection Support LonzaIN - Hyderabad 9d Ensures compliance with cGMP and international regulatory requirements by providing quality oversight for global growth projects and CAPEX investments, acting as the Global QA representative.
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Senior Manager, Third Party Manufacturing AbbVieCampoverde, Lazio, it 9d Lead relationships and performance of third-party manufacturers to ensure supply continuity, quality, and cost competitiveness for externally manufactured products.
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Manager Quality Assurance Operations (m/f/d)↗ SandozHolzkirchen, BY, DE $54k–$101k10d Manage QA operations, GMP compliance, and batch release processes for biosimilar and generic medicines.
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Operational Quality Manager GsknchIndonesia - DKI Jakarta - Jakarta Timur 10d Lead Quality Assurance activities across manufacturing, packaging, testing, and warehousing to ensure product compliance and safety.
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Sr. Associate, Quality Assurance & Regulatory Affairs AlconHong Kong 10d Ensure product compliance with global, local, and internal regulations and quality standards for medical devices and pharmaceuticals.
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Senior Quality Specialist General Medicine VIE Contract SanofiFramingham, MA 10d Ensure quality and regulatory compliance for products manufactured by external contractors in North America, managing audits, agreements, and continuous improvement.
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Quality Release Specialist↗ Norwich Pharmaceuticals IncNorwich, NY, US $62k–$62k10d Supports the release process to ensure delivery against plant and Quality Assurance goals by performing commercial releases for raw materials, package components, semi-finished, and finished products.
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Manager, Quality Assurance (Audit & Supplier Quality) *PC 484↗ Miltenyi BiotecGaithersburg, MD, US $110k–$110k10d Establish and manage the Bioindustry Quality System, leading strategic quality initiatives, risk-based auditing, and supplier quality oversight for a global network of sites and suppliers.
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Quality Systems Manager↗ West Pharmaceutical ServicesGreenfield, IN, US 10d Leads governance, compliance, and continual improvement of the Quality Management System (QMS) for a pharmaceutical manufacturing site in Indiana.
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Quality & Compliance Lead JllGurabo, PR 10d Primary driver for implementing, maintaining, and continuously improving Regional Quality & Compliance Programs across assigned sites in FDA-regulated manufacturing environments.
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Chargé(e) de Libération Thérapeutiques H/F SeptodontSaint-Maur-des-Fossés, FR 10d Review and release of therapeutic product batches (internal and outsourced) to ensure safety and regulatory compliance for patients.
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Quality Assurance Associate - Midwest Stem Cell KumcKansas City Metro Area $0k–$0k10d Ensures compliance with FDA and regulatory standards for a GMP/GTP stem cell therapy facility by managing quality assurance, regulatory documentation, and internal audits.
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Specialist I, QA Operations ForgebiologicsThe Hearth - Columbus, OH 10d Ensuring compliance with regulatory requirements and maintaining quality standards for AAV gene therapy manufacturing operations.
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