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Healthcare
› Quality and Validation
Quality and Validation
694 open positions
Quality Training Coordinator
Empowerpharmacy
Houston, TX
2mo
Coordinate training systems, logistics, and documentation to ensure compliant, consistent workforce readiness for a 503A/503B pharmaceutical compounding facility.
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Biotechnologist Trainee (Career Conversion Program)
Sanofi
City of Singapore
2mo
Execute routine cGMP manufacturing activities and operate automated systems in Upstream, Downstream, and Central Manufacturing Services processes for vaccine and biologics production.
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Specialist I&II, Manufacturing
AstraZeneca
Suzhou - Biopharmaceutical Industrial Park, CN
2mo
Execute core cell therapy manufacturing operations including cell sorting, culture, transduction, purification, formulation, and cryopreservation to complete cell product production tasks according to plan.
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Director, Manufacturing
Lonza
Remote
$199k–$199k
2mo
Develop and execute operational readiness strategy for bioconjugate drug substance manufacturing facilities, ensuring GMP compliance and inspection readiness for clinical and commercial production.
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Filling Set-up Sr. Technician, Operations (2nd Shift) - Onsite
Msd
USA - New Jersey - Rahway
$68k–$68k
2mo
Hands-on setup, operation, and troubleshooting of sterile filling lines, lyophilization, and capping equipment in a cGMP pharmaceutical manufacturing environment.
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Manager, Lab Systems
Amgen
India - Hyderabad
2mo
Lead a team providing operational support and system ownership for laboratory systems in a biopharmaceutical manufacturing environment, ensuring GMP compliance and system reliability.
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QC Associate Role (Fixed Term)
Thermofisher
Bishop's Stortford, United Kingdom
2mo
Perform QC inspections, documentation reviews, and inventory updates to ensure compliance with UK/EU GMP and regulatory standards for pharmaceutical and biological products.
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Quality Lead Technician
Takeda
USA - GA - Augusta
$0k–$0k
2mo
Ensures source plasma manufacturing consistency and compliance with cGMP regulations at a plasma center.
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Equipment Operator, Pre-Coding - 2nd Shift
Thermofisher
Bohemia, New York, USA
$0k–$0k
2mo
Operate automated and non-automated inkjet equipment to pre-code variable and static text on clinical trial labels for the pharmaceutical and biotechnology industry.
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Change Control Specialist
Regeneron
RENSSELAER
$62k–$62k
2mo
Develop strategic plans for change control and implement robust corrective actions to support manufacturing operations.
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Compliance & Facilities Engineer
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Anter Consulting Pte. Ltd.
Singapore, S00, SG
2mo
Operation and maintenance of site facilities within a GMP manufacturing environment with a strong emphasis on regulatory compliance.
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Pharmaziepraktikum im Bereich der Herstellung klinischer Prüfpräparate ab November 2026 (m/w/d)
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Merck Healthcare
Darmstadt, Hesse, Germany
2mo
Six-month pharmacy internship in Drug Product Excellence, focusing on manufacturing solid and sterile dosage forms for clinical trials.
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Quality Operations Manager-Ultrasound
Philips
Reedsville, Pennsylvania, United States
$120k–$120k
2mo
Managing quality operations, CAPA processes, and site compliance for ultrasound transducer manufacturing.
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Werde Teil unseres Talentpools für zukünftige Qualified Persons (QPs) / Sachkundige Personen (all genders)
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AbbVie
Ludwigshafen, Rhineland-Palatinate, Germany
2mo
Central role in pharmaceutical quality assurance, responsible for batch release and certification of medical products in R&D or Operations.
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Pharmaziepraktikum gemäß §4 Approbationsordnung für Apotheker im Bereich Qualitätssicherung (m/w/d)
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Merck Healthcare
Darmstadt, Hesse, Germany
2mo
Pharmacist internship focusing on quality assurance systems, Good Manufacturing Practice (GMP) implementation, and risk management within a pharmaceutical manufacturing environment.
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Equipment Validation Specialist, Level III
Lonza
US - Portsmouth, NH
2mo
Ensures critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters, and global regulatory guidelines to support compliant biopharmaceutical manufacturing.
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Leitung der Herstellung klinischer Prüfpräparate Parenteralia (all genders) (Vollzeit, unbefristet)
AbbVie
Ludwigshafen, RP, de
2mo
Leading the manufacturing of parenteral clinical trial preparations (vials and syringes) under GMP regulations.
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Label Change Associate
ConvaTec
Michalovce, Slovakia
$14k–$14k
2mo
Coordinate and implement market- and compliance-driven packaging and label changes for finished goods, ensuring production-ready graphics are delivered on time.
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Spezialist Qualifizierung Pharmazeutischer Anlagen (w/m/d)
Takeda
AUT - Wien - Lange Allee 24
$0k–$0k
2mo
Qualification of pharmaceutical equipment, processes, and production lines to ensure quality standards and patient safety.
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Senior technicien USP weekend
Thermofisher
Seneffe, Belgium
2mo
Weekend technician executing Upstream Processing (cell culture) activities in a cGMP biopharmaceutical environment to support clinical batch production.
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IRE_Qualified Person
Pciservices
Stamullen, Co. Meath, IRL, IE
2mo
Certifying investigational medicinal products and ensuring compliance with EU GMP and regulatory requirements for clinical trial supplies.
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Quality Operations Manager
Pciservices
Stamullen, Co. Meath, IRL
2mo
Lead quality operations and regulatory compliance for a biopharma company, overseeing batch manufacturing records, deviation management, and customer quality agreements.
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cGMP Vector Manufacturing Associate
Usc
Los Angeles, CA - Health Sciences Campus, US
$0k–$0k
2mo
Production and purification of viral vectors under cGMP guidelines, including cell culture, media preparation, cryopreservation, and aseptic processing.
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Senior ATMP-GMP Consultant / Projektmanager (m/w/d)
Syntegon
Frankfurt am Main, HE, de
2mo
Senior consultant and project manager leading complex GMP projects in the ATMP (Advanced Therapy Medicinal Products) sector, ensuring regulatory compliance and quality for clients.
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GMP-Consultant (m/w/d)
Syntegon
Frankfurt am Main, HE, de
2mo
Provide GMP consulting services, develop tailored solutions, and lead ATMP-GMP projects for biopharmaceutical clients.
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Associate Director, Shift Quality Operations (Onsite)
Vrtx
Boston, MA
$154k–$154k
2mo
Advanced technical resource providing shift-based quality leadership and oversight for aseptic cell therapy manufacturing operations to ensure cGMP compliance and safe production.
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(Pharmazie-)Praktikum Medical in-use, Pharmaceutical Dev. Biologicals
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Boehringer Ingelheim
Biberach an der Riß, Baden-Württemberg, Germany
2mo
Supporting the investigation of Medical In-Use studies to assess the compatibility and stability of new biological drugs (Biologicals and ATMP) with medical devices during clinical development.
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Team Lead, Kit Production
Thermofisher
Vilvoorde, Belgium
2mo
Lead operations for clinical trial kit production, ensuring quality, efficiency, and timely fulfillment of supplies for global pharmaceutical and biotech clients.
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Pharmazeut im Praktikum - Global Quality Systems & Compliance (w/m/d)
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Stada Group
Bad Vilbel, Hesse, Germany
2mo
Intern supporting the definition, maintenance, and development of Quality Management Systems (QMS) and Quality Compliance for global pharmaceutical manufacturing.
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Associate Director, Viral Vector Process Development, Upstream
AstraZeneca
US - Gaithersburg - MD
$138k–$138k
2mo
Lead end-to-end upstream design, development, and scale-up of Lentiviral Vector (LVV) manufacturing processes for AstraZeneca's Cell Therapy portfolio, focusing on suspension bioreactor platforms from research through commercial readiness.
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Validation Analyst 1
Pciservices
Rockford, IL, USA
$0k–$0k
2mo
Managing validation projects for small customer accounts to ensure compliance with government and customer requirements in the biopharma industry.
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GRADUATE ENGINEERING TRAINEE
Gehc
Bengaluru
2mo
Manage ultrasound/PCS product manufacturing lines, resolve quality issues, and ensure equipment calibration and validation activities.
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Spécialiste Validation
Galderma
Baie-D'Urfé
2mo
Ensuring qualification and maintenance of validated status for equipment, processes, and systems at a pharmaceutical manufacturing site.
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Lean Six Sigma Blackbelt
Zoll
Chelmsford, MA
$115k–$115k
2mo
Leads cross-functional teams to improve process efficiencies and effectiveness through Lean and Six Sigma projects, driving sustainable results and business impacts.
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Clinical Program Quality, Associate Director, R&D, China
Takeda
2 Locations
2mo
Oversees quality assurance for global and local clinical research programs in R&D, Plasma Derived Therapy, Vaccines, and Oncology to ensure inspection readiness.
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Project CQV Manager-Biopharma
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Process Engineering Specialists Pte. Ltd.
Singapore, S00, SG
2mo
Lead and manage the full CQV lifecycle for large-scale biopharmaceutical manufacturing projects, ensuring compliance with GMP and regulatory requirements during commissioning and qualification phases.
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QC Environmental Monitoring - Bari
Eurofins
Modugno, Apulia, it
2mo
Support pharmaceutical production processes by performing environmental monitoring via media fill tests and microbiological monitoring in controlled areas.
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Ingénieur Assurance Qualité Environnementale H/F
AbbVie
Annecy, Auvergne-Rhône-Alpes, fr
2mo
Environmental Quality Assurance Engineer supporting sterile injectable production and R&D projects in cleanrooms and utilities.
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Technician - Biomanufacturing, Central Services
Catalent
Madison, WI
2mo
Entry-level technician performing basic buffer preparation, weighing raw materials, and executing manufacturing procedures in a clean room environment to produce biopharmaceutical products.
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Ausbildung als Pharmakant*in in Ingelheim 2027
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Boehringer Ingelheim
Ingelheim am Rhein, Rhineland-Palatinate, Germany
$1k–$1k
2mo
3.5-year vocational training to learn pharmaceutical manufacturing processes, production of dosage forms (capsules, tablets, inhalers), and quality control of medicines.
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Drug Production, Associate Manufacturing Specialist
Regeneron
RENSSELAER
$0k–$0k
2mo
Manufacturing life-changing biopharmaceuticals including therapeutic proteins and monoclonal antibodies in a clean room environment.
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Drug Production, Associate Manufacturing Specialist (Overnights)
Regeneron
RENSSELAER
$0k–$0k
2mo
Manufacturing life-changing biopharmaceuticals, specifically monoclonal antibodies, in a clean room environment.
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Pharmazeut im Praktikum Pharmazeutische Industrie (m/w/d) in Bad Boll (nahe Stuttgart)
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Wala
Remote
2mo
Practical year internship for pharmacists in pharmaceutical industry, supporting product development, quality management, regulatory affairs, and marketing.
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Associate Director, Quality Systems - Cell and Gene Therapies (VCGT)
Vrtx
Boston, MA
$148k–$148k
2mo
Strategic design and tactical execution of quality systems, risk management, and quality culture for the Vertex Cell and Gene Therapy (VCGT) organization.
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Responsable Technique – Produits Semi-Solides /Technical Manager Process – Semi-Solid
Galderma
Baie-D'Urfé
2mo
Technical manager overseeing the lifecycle and manufacturing processes of semi-solid cosmetic products, serving as the primary interface between Galderma and external contract manufacturers.
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Lead Operator
Thermofisher
Newport, United Kingdom
2mo
Lead the day-to-day running of a manufacturing team to ensure safe, organized operations, high-quality output, and plan adherence at optimal cost.
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Sterilization and Microbiology Specialist
Novanta
Prelouc, Czech Republic
2mo
Establish and monitor cleanroom protocols (ISO7/ISO8), validate sterilization cycles, and release final medical device products for distribution.
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Supervisor, Production Support - Large Scale Allogenic Manufacturing
Lonza
US - Portsmouth, NH
2mo
Coordinate safety, quality, and daily manufacturing operations for cGMP cell therapy production, providing real-time floor oversight and team leadership.
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Senior Manager, ECQ Delivery
Bristolmyerssquibb
Summit West - NJ - US
2mo
Senior Manager leading Equipment Commissioning & Qualification (ECQ) teams to validate pharmaceutical manufacturing and laboratory equipment, facilities, and computerized systems in compliance with cGMP and GXP regulations.
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Clinical Compliance Manager
Thermofisher
Remote, Mexico
2mo
Strategic quality leader ensuring clinical research operations meet GxP regulations and global standards through audits, risk management, and continuous improvement.
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