Quality and Validation
680 open positions
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Senior Associate - Biomanufacturing, Compliance - Manufacturing Technical Support CatalentMadison, WI 2mo Lead rapid response as incident commander for biomanufacturing operations, ensuring compliant GMP execution and delivering high-quality biologics.
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Lead Operator, Manufacturing - (Mon-Wed Nights) ThermofisherCincinnati, Ohio, USA 2mo Lead manufacturing operations for pharmaceutical products including equipment setup, operation, cleaning, and maintenance in a cGMP environment.
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Computerized Systems Validation Specialist SharpservicesHamont-Achel 2mo Ensuring all IT systems impacting Good Manufacturing Practices (GMP) are in a validated state and managing the validation lifecycle for software and hardware changes.
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Executive Director, Microbiology Quality Sterility Assurance BristolmyerssquibbPrinceton - NJ - US $261k–$261k2mo Global leadership role defining and governing the enterprise-wide Contamination Control Strategy (CCS) and sterility assurance framework across pharmaceutical, biopharmaceutical, cell therapy, and radiopharmaceutical manufacturing sites.
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Pharmaceutical Manufacturing Technician EurofinsGroton, CT, us 3mo Execute complex bulk product manufacturing activities to convert raw materials into intermediate and final patient-ready presentations, including equipment setup, operation, and maintenance in a classified manufacturing space.
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Pharmaceutical Specialist Teva PharmaceuticalsHaarlem, Noord-Holland 3mo Ensuring quality, compliance, and continuous improvement of pharmaceutical manufacturing processes through investigations and root cause analysis.
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Pharmaziepraktikum in der Forschung und Entwicklung AbbVieLudwigshafen, RP, de 3mo Research and development internship for pharmacy students to gain insights into drug development processes, regulatory compliance, and formulation technologies.
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Technicien Process H/F - CDI - Chatillon sur Chalaronne ViatrisChatillon-sur-Chalaronne, Auvergne-Rhone-Alpes, France $0k–$0k3mo Supporting the lifecycle of pharmaceutical products by conducting pilot-scale manufacturing, performing technical analyses, and validating processes for dry dosage forms.
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Quality Site Head AlnylamUnited States 3mo Lead the Quality organization for a manufacturing and testing facility, ensuring compliant product supply and operational excellence for clinical and commercial operations.
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Clinical Research Coordinator II – Cellular Manufacturing UchicagoChicago, IL $60k–$60k3mo Manufacture clinical-grade cellular therapies and vaccines for Phase I–III clinical trials in a cGMP facility.
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Interim Responsible Pharmacist France (m/f/d) Redcare PharmacyFrance 3mo Interim Responsible Pharmacist ensuring regulatory compliance, quality, and safety of pharmaceutical services and products during the absence of the main Responsible Pharmacist.
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Manager*in GMP Compliance – Oligonukleotide (m/w/d) Lgc-GroupBerlin, BE, de 3mo Ensure GMP compliance and develop standards for oligonucleotide production.
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Batch Release Pharmacist Beautiful RecruitmentPont-du-Château, Clermont-Ferrand 3mo Oversee batch certification and release activities to ensure product quality and regulatory compliance for medicinal products.
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Pharmacist
Molecule.XyzDeutschland
3mo
Designing and validating precisely-dosed formulations of cognitive, performance, and longevity compounds (oral solids and sterile injectables) to establish shelf life and quality standards.
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Drug Product Manufacturing Associate I - 1st Shift PciservicesUSA_CA_San Diego_Lusk $0k–$0k3mo Executing GMP production of injectable pharmaceuticals in a clean room environment, operating complex manufacturing equipment, and maintaining strict documentation standards.
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MSAT Lead 80-100% LonzaCH - Stein 3mo Lead MSAT team through CAPEX growth project ramp-up, driving PPQs, aseptic process simulations, and equipment qualifications for sterile fill & finish lines.
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Pharmazie-Praktikum im Bereich Pharma Packaging↗ Daiichi Sankyo Europe GmbHPfaffenhofen an der Ilm, Bavaria, Germany 3mo Pharmacist internship focusing on production and packaging processes, digitalization, and quality assurance in a pharmaceutical company.
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Profili in ambito farmaceutico/biomedicale- Appartenenti alle categorie p LhhProvincia di Milano, Lombardia 3mo Recruitment of professionals from protected categories (L.68/99) for various roles in the pharmaceutical and biomedical sectors.
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Apotheker (m/w/d) im praktischen Jahr↗ Fresenius Medical CareSt. Wendel, Saarland, Germany 3mo Ensuring compliance with GMP and FDA requirements for the manufacturing of dialysis membranes, filters, and solutions.
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Director, VTR Biologics and AIV BiibhrResearch Triangle Park, NC $178k–$178k3mo Lead VTR (Validation, Transfer, and Registration) and AIV (Analytical Instrument Validation) teams to ensure analytical readiness for late-stage clinical and commercial biologics and combination drug products.
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Manager Quality Control Microbiology & Biochemistry OrganonNLD - Oss - Molenstraat 3mo Leading a team to ensure microbiological safety, pharmacological activity, and biochemical quality control of pharmaceutical and biotechnological products via in vivo bioassays and sterility testing.
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National Air Logistics Healthcare Quality Manager (m/w/d) Kuehne+NagelFrankfurt am Main, Hessen $0k–$0k3mo Ensuring highest quality standards in air logistics for life-critical medications to guarantee safe, intact, and punctual delivery to patients.
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Pharmazeut (m/w/d) im Praktikum in der Produktion MsdDEU - Niedersachsen - Friesoythe, DE 3mo Pharmaceutical production intern creating documentation, SOPs, and reports while supporting deviation handling and quality implementation.
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Skrbnik osnovnih podatkov materialov / Site Master Data Expert (m/ž/d) NovartisLjubljana 3mo Managing the lifecycle of basic material data to ensure data accuracy, compliance, and timely availability for production excellence.
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Production / Manufacturing Operations RegeneronLimerick $0k–$0k3mo Performing tasks in a fully gowned, cleanroom environment to support clinical and commercial manufacturing programs, including equipment cleaning, in-process sampling, and batch record completion.
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VP Quality, Global Life Sciences EcolabUSA - Pennsylvania - King of Prussia $250k–$250k3mo Enterprise quality vision, strategy, and operating model for Ecolab's Life Sciences business (Bioprocessing, Purification, Pharma, Personal Care), ensuring product quality, patient safety, and regulatory compliance across a global manufacturing network.
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Tech Transfer Lead- BioPharma Process Engineering SpecialistsSingapore 3mo Lead technology transfer activities from process development teams to manufacturing sites in the Life Sciences industry, ensuring GMP compliance and operational readiness.
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FSQ Raw Manager Jack-Link-S-Protein-SnacksPerry, GA, us $94k–$94k3mo Controlling upstream biological, process, and supplier risks in raw material operations to ensure food safety and operational stability before products enter downstream processing.
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Associate Director, Sterility Assurance ModernaTXNorwood, Massachusetts $143k–$143k4mo Senior technical role accountable for the design, implementation, and oversight of the site's Contamination Control Strategy (CCS) program to ensure sterility assurance activities align with regulatory expectations and aseptic manufacturing best practices.
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Customer Service Technician ( Perfil Eléctrico - electromecánico) SyntegonMadrid, MD, es 4mo Execute service orders for environmental control testing and equipment commissioning in cleanrooms and controlled environments to ensure pharmaceutical industry compliance.
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2nd pharmacist Spits Apeldoorn CencoraNederland 4mo Support quality-related activities and act as acting pharmacist for the Spits Apeldoorn facility, ensuring compliance with pharmaceutical standards.
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Operatør Aseptisk avdeling GehcOslo, NO 4mo Operate machinery and equipment for aseptic production of pharmaceutical products in classified cleanrooms (Classes A, B, C, D) while adhering to strict hygiene and process protocols.
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Manager, C&Q Document Preparation (Facilities and Utilities) AmgenIndia - Hyderabad 4mo Lead the preparation and delivery of commissioning and qualification (C&Q) documentation to support GMP manufacturing, packaging, and facility systems across Amgen's operations.
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