Quality and Validation
1,404 open positions
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Packaging Associate Par HealthKanchipuram, Tamil Nadu 14d Supervising packing operations, production activities, and quality compliance in a manufacturing environment.
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Technicien Culture Cellulaire USP (F/H/X) - Poste basé à Bordeaux AbbVieLyon, Auvergne-Rhône-Alpes, fr 15d Operate cell culture activities in a GMP-compliant bioproduction environment using single-use technologies to produce therapeutic proteins.
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Consultant en Assurance Qualité Réglementaire (Industrie Pharmaceutique) F/H AXSANTParis, Ile-de-France 15d Pilot the Change Control process for a pharmaceutical manufacturing site, covering initiation, screening, impact assessment, risk assessment, regulatory assessment, action planning, approval, and implementation.
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Consultant assurance de stérilité F/H COPHACLEANLyon, Rhône 15d Define global sterility assurance strategy, pilot contamination control deployment, and manage risk analyses for pharma clients near Lyon.
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Ingénieur Métrologie H/F/X MY RECRUTEURIndre-et-Loire, Centre 15d Ensuring compliance of production facilities, equipment, and environments with GMP and regulatory standards in the pharmaceutical industry.
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Microbiology Development & Technical Transfer Specialist EurofinsLjubljana, Ljubljana, si 15d Microbiology subject matter expert supporting pharmaceutical products from development through commercialization, ensuring microbiological requirements are integrated throughout the product lifecycle.
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CQV Manager - Pharmaceutical Manufacturing Turner & TownsendSingapore, Asia, sg 15d Lead commissioning, qualification, and validation (CQV) strategies and execution for large-scale pharmaceutical manufacturing capital projects, ensuring GMP compliance and operational readiness.
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Scientist I, Formulation ThermofisherRockford, Illinois, USA 15d Execute manufacturing protocols and large-scale formulation activities for Thermo Fisher Scientific products in a GMP/ISO-regulated laboratory and cleanroom environment.
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Pharmazeut als Sachkundige Person (m/w/d)↗ RecipharmWasserburg am Inn, Bavaria, Germany 15d Responsible for batch release for further processing, shipping, and transport as a Qualified Person (QP), including batch record review and quality assurance measures.
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Training Client Manager, Holly Springs RocheHolly Springs, US $94k–$174k15d Develop and implement site-specific training content, process ownership, and learning development efforts for a new manufacturing site launch.
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Packaging Development Scientist↗ RemedicaLimassol, Limassol, Cyprus 15d Develop and optimize pharmaceutical packaging systems to ensure product stability, regulatory compliance, and sustainability for generic medicines.
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Launch Technician↗ Insud PharmaMadrid, Community of Madrid, Spain 15d Coordinate technical launch activities, support technology transfer, and ensure compliance for new pharmaceutical product launches.
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Associate Specialist, Engineering - 2nd Shift (Onsite) MsdUSA - New Jersey - Rahway 15d Support the design, commissioning, and operations of a new sterile clinical manufacturing facility for small molecules, biologics, and vaccines.
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Produktionsmitarbeiter - pharmazeutische Herstellung (m/w/d) AqVida GmbHDassow, MECKLENBURG_VORPOMMERN 15d Manufacturing of oncology generic drugs in a modern production facility using closed isolators and filling lines.
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Pharmamitarbeiter (m/w/d) im Bereich Pankreatin Vollzeit, zunächst befristet auf 24 Monate Nordmark Pharma GmbHUetersen, SCHLESWIG_HOLSTEIN 15d Operate and monitor extraction, filtration, and drying equipment to manufacture biological active ingredients in a GMP-compliant environment.
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Preparador Técnico - Contrato Temporário↗ HovioneLoures, Lisbon, Portugal 15d Responsible for pharmaceutical product production activities, including scale-up and development of production processes for clinical trial materials in compliance with GMP standards.
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Manager, QA Laboratory Operations BristolmyerssquibbCruiserath - IE 15d Manager leading QA oversight for sterile drug product manufacturing start-up and commercial operations, ensuring GMP compliance and product release.
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Junior/Senior Executive – Quality Assurance (Bio Technology )↗ Tulsi TherapeuticsHyderabad, Telangana, India 15d Support GMP quality operations for mesenchymal stem cell (MSC) and exosome-based products in a biotechnology startup.
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Supervisor, Production BaxterOxford, Oxfordshire, GB 15d Lead manufacturing teams responsible for aseptic compounding of products supplied across the UK and Ireland in Grade A-D cleanroom environments.
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PTA (w/m/d) für die Qualitätssicherung in der Herstellung↗ Eurimpharm Arzneimittel GMBHSaaldorf-Surheim, Bavaria, Germany €33k15d Ensuring proper execution of all work steps in pharmaceutical repackaging and conducting final inspections of finished goods based on defined test plans according to GMP regulations.
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Early-Stage Drug Product Project Engineer↗ Lsc, Life Science ConsultantsDublin, County Dublin, Ireland 15d Deliver change-management packages, coordinate sampling/testing strategies, and manage material readiness for low-volume bulk API manufacturing of mammalian cell culture derived APIs for Phase III clinical trials and product launch.
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Product and Technology Lead↗ HaleonDungarvan, County Waterford, Ireland €70k–€96k15d Lead a team of Product and Process Engineers and Packaging Engineers to manage the lifecycle of products manufactured on site, ensuring processes and raw materials are qualified and compliant.
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Manufacturing Operator LonzaUS - Tampa, FL 15d Operate manufacturing equipment to produce solid oral dosage products (tablets and capsules) in a cGMP-compliant pharmaceutical environment.
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Manager, QA Laboratory Operations↗ Bristol Myers Squibb UK & IrelandCounty Dublin, Ireland 15d Manager leading QA oversight for sterile drug product manufacturing start-up and commercial operations, ensuring GMP compliance and product release.
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Processing Operator 1 - Night Shift - Fixed term 12 months KenvueNorth America, Canada, Ontario, Guelph $36k–$58k15d Operate manufacturing equipment to produce bulk pharmaceutical products including tablets, liquids, and coated products in a regulated environment.
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Pharmaziepraktikant*in im Bereich Cartridge Platform Development Mai 2028 SanofiFrankfurt am Main, DE 15d Support the technical development of primary packaging systems for injectables and their functional system analysis within the Medical Device Development team.
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Facility & Utilities Manager, Abbott Healthcare Vietnam AbbottVietnam - Ho Chi Minh City 15d Ensure reliable, compliant, and efficient operation of all facility, utility, HVAC, and BMS systems supporting GMP manufacturing and laboratory operations.
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Technical Staff Piramal PharmaMadhya Pradesh, India 15d Supervises coating activity quality products manufacturing in conformance with c-GMP/safety and hygiene requirements on a shift-to-shift basis.
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Assistant, Manufacturing Injectables AmnealIndia 15d Processing and assembly of ingredients and pharmaceutical products in a regulated manufacturing environment.
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Production Manager (Secondary Packaging & Redressing Operations) Zuellig PharmaSingapore 15d Lead GMP secondary packaging and redressing operations to ensure timely delivery of customer requirements while maintaining quality, compliance, and safety standards.
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Senior Officer, Manufacturing Injectables Amneal PharmaceuticalsAhmedabad, Gujarat 15d Operate and monitor injectable manufacturing equipment to process and assemble sterile pharmaceutical products in a regulated environment.
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Operaria/o de Limpieza de materiales. Laboratorio Farmacéutico InmunotekSan Sebastián de los Reyes 16d Cleaning materials, rooms, and cleanroom surfaces for vaccine manufacturing in a pharmaceutical laboratory.
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Junior Production Engineer↗ Vallaurix Pte. Ltd.Clementi, S00, SG 16d Lead the development of next-generation pharmaceutical formulations, specifically injectable processes, supporting cGMP manufacturing and validation.
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Quality Assurance Specialist↗ Reig JofreSant Joan Despí, Catalonia, Spain 16d Ensuring product sterility and improving aseptic practices in a sterile manufacturing plant.
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Qualifizierungsexpert*in (alle Geschlechter) Bayer AG PharmaceuticalsLeverkusen, NORDRHEIN_WESTFALEN €54k16d Ensuring GMP-compliant use of production and HVAC (TGA) facilities and equipment through structured qualification and documentation.
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Teamleitung Qualitätskontrolle - Spritzguss (m/w/d) Aptar Radolfzell GmbHRadolfzell am Bodensee, BADEN_WUERTTEMBERG 16d Leading the quality control team for injection molding operations, ensuring process development and handling deviations.
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Analista de Control en Proceso (IPC) en Industria Farmacéutica ( Temporal)↗ Talent Search PeopleBadalona, Catalonia, Spain 16d Performing sampling, inspection, and in-process control of traces, packaging materials, bulk product, and finished product in a pharmaceutical manufacturing environment.
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RESPONSÁVEL TÉCNICO (RT) – QUALIDADE / EMBALAGEM GMP↗ Blau FarmacêuticaJaboatão dos Guararapes, Pernambuco, Brazil 16d Act as the Technical Responsible for the Pernambuco Logistics Center, ensuring packaging, storage, and movement of pharmaceutical products comply with regulatory requirements, GMP, and internal procedures.
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Laborant/in in der Wirkstoff-Produktion WeylChem ORGANICA GmbHBitterfeld-Wolfen, SACHSEN_ANHALT 16d Manufacturing of active pharmaceutical ingredients (APIs) in cleanrooms, including packaging, sampling, in-process controls, and documentation under strict hygienic and GMP regulations.
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