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Healthcare
› Quality and Validation
Quality and Validation
1,404 open positions
Associate Specialist, Engineering (Onsite)
Msd
USA - New Jersey - Rahway
19d
Support sterile clinical manufacturing facility design, commissioning, qualification, and operations for drug product development.
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Senior Technical Specialist, MM (MFG)
Lonza
SG - Tuas, Singapore
19d
Develop and manage GMP manufacturing documentation (MBRs, SOPs, CRs) and lead technical investigations to ensure operational readiness and manufacturing excellence.
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Associate Manufacturing AME - Days
Amgen
US - Rhode Island - West Greenwich
19d
Perform cell culture, purification, weigh & dispense, and solutions batching tasks in drug substance plants at Amgen's Rhode Island facility.
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Associate Lead I - Biomanufacturing, Compliance
Catalent
Madison, WI, US
19d
Ensures compliance with cGMP, regulatory, and client requirements in biologics manufacturing operations.
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Senior Polymer Chemist
Thermofisher
Warrington (KG), United Kingdom
19d
Senior Staff Scientist in Manufacturing Sciences ensuring manufacturing quality, process validation, and regulatory compliance for biopharmaceutical/diagnostic solutions.
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Plasma Sampling Team Leader
Eurofins
Broadmeadows, VIC, au
19d
Provide operational leadership, technical oversight, and facility support for plasma sampling operations at a pharmaceutical manufacturing client site, ensuring efficient execution, sample management, and traceability in compliance with GMP.
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Senior Executive- Filling Inj Manufacturing
Amneal
India
19d
Ensuring compliance and operational integrity in sterile injectable manufacturing through document control, line clearance, and equipment monitoring.
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Senior Research Associate-FD
Piramal Pharma
India
19d
Formulation development and manufacturing of solid oral and other dosage forms for NCE, generic, and line extension projects.
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Manufacturing Operator III, UD Fill - B1 Shift
AbbVie
Waco, TX, us
19d
Operate and service automated manufacturing equipment in aseptic packaging environments to produce finished pharmaceutical products.
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Third Party Manufacturing, Account Manager, External Manufacturing Medical Devise
AbbVie
North Chicago, IL, us
19d
Primary interface between AbbVie and Third-Party Manufacturers (TPMs) or Third-Party Customers (TPCs) to manage contract manufacturing for pharmaceutical products, combination products, and medical devices.
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Manager / Senior Manager, Pharmacy (Compounding Hub, 2-Year Contract)
National University Polyclinics
Singapore
19d
Lead operational, governance, and business functions for Singapore's first GMP-compliant sterile drug compounding hub, producing ready-to-use compounded sterile products including parenteral nutrition, chemotherapy, and antibiotic admixtures.
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Assembly & Packaging Lead / Manager
Wuxi Biologics Biopharmaceuticals Singapore Private Limited
Singapore
19d
Lead startup, commissioning, validation, and operational readiness for Assembly, Visual Inspection, and Packaging operations in pharmaceutical manufacturing.
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Manufacturing Senior Manager, Drug Product Aseptic Filling Operation
WuXi Biologics
Singapore
19d
Leading the startup of a state-of-the-art aseptic manufacturing facility, overseeing production lines, equipment, and utilities to ensure compliant execution of critical aseptic processes.
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Senior Research Associate-FD
Piramal Pharma Ltd
Ahmedabad, Gujarat
19d
Formulation development and manufacturing of solid oral and other dosage forms for drug discovery, generic, and line extension projects.
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Jr Validation Analyst
Catalent
Brasil
20d
Execute GMP Compliance activities ensuring alignment with relevant legislation, corporate guidelines, and internal procedures.
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Prozessingenieur*in - Reinraum & HVAC (m/w/d)
Lgc-Group
Berlin, de
20d
Ensure technical integrity and availability of GMP-compliant cleanroom infrastructure (HVAC, monitoring, airlocks) for RNA therapeutic production.
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Pharmaceutical Scientist – Consultancy Assignment at AstraZeneca
Randstad AB
Södertälje, Sweden
20d
Support changes and issues for commercial oral solid drug products by analyzing analytical results and process information across manufacturing sites, supporting regulatory inquiries, and facilitating technical risk assessments.
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Pharmaceutical Scientist to AstraZeneca
Qrios AB
Stockholm, Sweden
20d
Support changes and issues for commercial oral solid drug products by analyzing finished product analytical results and process information across multiple manufacturing sites.
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Manager - Material Process Delivery
Pg
JAKARTA GENERAL OFFICE, ID
20d
Lead technology transfer, process validation, and lifecycle management for pharmaceutical products across contract manufacturing sites in the Asia, Middle East, and East Africa region.
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Mitarbeiter (m/w/d) in der GMP Herstellung
Kölsche Blister GmbH
Köln, NORDRHEIN_WESTFALEN
20d
Manufacturing of patient-specific pharmaceutical blisters in a GMP-compliant environment.
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Techniker/in - Chemietechnik (ohne Schwerpunkt)
Seibersdorf Labor GmbH
Seibersdorf, NIEDEROESTERREICH
€46k
20d
Manufacturing radiopharmaceuticals under GMP guidelines and operating/maintaining technical production equipment to ensure reliable supply of high-quality drugs to patients.
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Reinraumkoordinator (w/m/d)
Jenoptik AG
Jena, THUERINGEN
20d
Cross-functional coordination and management of cleanroom environments, ensuring compliance, maintenance, and operational standards for optical production.
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Sr. Production Technician
Lonza
CN - Nansha
20d
Execute production operations, equipment maintenance, and sampling in a pharmaceutical manufacturing environment to ensure safety, GMP compliance, and efficient plan completion.
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Biotechnologist 1
Lonza
UK - Slough
20d
Support pilot-scale biopharmaceutical manufacturing operations, ensuring safe and efficient execution of upstream and downstream processing activities.
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2027 Summer Co-op HSE Health Safety Environment Swiftwater PA
Sanofi
Swiftwater, PA, US
$73k–$94k
20d
Support HSE operations in large-scale vaccine manufacturing, OPEX/CAPEX projects, contractor safety, and R&D laboratory activities with a primary focus on Environmental Compliance.
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Wissenschaftliche Leitung (m/w/d) der radiopharmazeutischen Herstellung am Zyklotron der JGU
Johannes Gutenberg-Universität Dienststellen: 9000 - 9640
Mainz am Rhein, RHEINLAND_PFALZ
20d
Lead the production and synthesis of short-lived Fluor-18 for radiopharmaceutical imaging (PET) at a university cyclotron, ensuring GMP compliance and quality management.
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Biochemiker/in
BOEHRINGER INGELHEIM RCV GmbH & Co KG
Wien,Meidling, WIEN
€48k
20d
Monitoring and executing process-controlled production steps in biopharmaceutical manufacturing, including in-process controls and large-scale equipment operation.
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Lyophilization Operator I (12-Hour Overnight Shift)
Freseniusglobal
Melrose Park, IL, US
20d
Operating lyophilization and terminal sterilization cycles for pharmaceutical products in a clean room environment.
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Process Assessment and Validation Scientist II
Lonza
NL - Geleen
€48k–€67k
20d
Performing process assessments and validation activities for new process implementation and post-Technology Transfer support in a CGT manufacturing facility.
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Associate Director, Aseptic Facility and Utility Design
Bms
New Brunswick - NJ - US
$162k–$210k
20d
Global Quality SME for aseptic facility and utility design, defining enterprise standards and overseeing contamination control strategies for cleanrooms, barrier systems, and critical utilities in pharmaceutical manufacturing.
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Associate - Biomanufacturing, Upstream
Catalent
Madison, WI, US
20d
Perform upstream cell culture activities, aseptic manipulation, and basic troubleshooting in a controlled GMP environment to produce biologic therapies.
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Microbiology & Environmental Monitoring (EM) Supervisor
Jabil
Hunt Valley, MD, US
$81k–$147k
20d
Leads the site microbiology laboratory and contamination control program for sterile and non-sterile pharmaceutical manufacturing, ensuring cleanrooms, utilities, and products meet cGMP, FDA, EU GMP Annex 1, and USP requirements.
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Lab Technician (Nights)
Cardinalhealth
OH-Columbus PET-OSU, US
$44k
20d
Manufactures time-sensitive radiopharmaceuticals and radioactive isotopes in a highly regulated nuclear environment to support patient diagnosis and treatment.
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M&S-Head of Inspection PCU _Fill & Finish-Beijing
Sanofi
Beijing, CN
20d
Lead the Inspection Process-Centric Unit (PCU) for Fill & Finish operations, ensuring 24/7 production performance, quality compliance, and continuous improvement in a sterile manufacturing environment.
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Senior Packager, Pilot
Edwards
USA - California – Irvine
$45k
20d
Perform packaging operations for cardiovascular medical devices, ensuring quality and regulatory compliance in a clean room environment.
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Supply Chain Coördinator
State of Oregon
België
20d
Coordinate artwork processes and component lists for pharmaceutical packaging production.
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Manufacturing Senior Associate_104865
MyCareernet
Hyderabad, Telangana
20d
Managing the lifecycle of controlled GMP documents for manufacturing operations, ensuring accuracy and compliance across SOPs, protocols, and deviation records.
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Pharmaceutical Scientist AstraZeneca
Tessero Sweden AB
Södertälje, Sweden
21d
Support changes and issues for commercial oral solid drug products by analyzing finished product analytical results and process information across multiple manufacturing sites.
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Pharmacien(ne) adjoint - Titulaire d'une spécialisation en pharmacie d'industrie H/F/X
CHR HAUTE SENNE
Zinnik
21d
Develop, implement, and monitor qualification and validation activities for cleaning and production processes in pharmaceutical preparation zones.
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Assistant qualité en Production (H/F)
Manpower
Liancourt, Clermont
21d
Support production quality objectives in the pharmaceutical industry by reviewing batch files, monitoring stock movements, and training packaging operators.
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Manufacturing Shift Lead
Takeda
Singapore
21d
Lead routine and critical manufacturing operations in Cell Culture and Purification areas for commercial and clinical biopharmaceutical products.
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Manufacturing Technician II
Thermo Fisher Scientific
Singapore
21d
Assemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.
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Training and Documentation Specialist
Sanofi
Singapore
21d
Develop and deliver GMP training programs and manage the GxP documentation lifecycle for a highly digitalized vaccine and biologics production facility.
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Microbiology Manager
↗
Valtera Group Ltd
Remote
21d
Lead microbiology investigations, drive root cause analysis, and manage equipment qualification projects in a sterile pharmaceutical/biologics manufacturing environment.
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Ingeniero de documentación
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Probiomed Sa de Cv
Santo Tomás, DIF, MX
$156k
21d
Managing documentation and regulatory compliance for maintenance and critical services in a biopharmaceutical manufacturing plant.
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Sr. Manager, Quality Control Microbiology
↗
Abelzeta Inc
Rockville, MD, US
21d
Directing all QC microbiology operations supporting Phase I/II/pivotal clinical manufacturing and commercial readiness, including environmental monitoring, facility qualification, aseptic process qualification, and Contamination Control Strategy governance.
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Manager/Senior Manager, Quality Control - Microbiology
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Genezen
Lexington, MA, US
$130k–$150k
21d
Manage the Microbiology laboratory and personnel, executing Environmental and Personnel Monitoring programs for GMP viral vector production and gene therapy clinical trials.
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Qualitätsmanager (m/w/d) Reinraum in Mannheim
Apleona Infra Services GmbH
Mannheim, BADEN_WUERTTEMBERG
€55k–€60k
21d
Ensuring quality assurance in regulated environments (cleanrooms, laboratories) for a large pharmaceutical company in Mannheim, including monitoring cleaning documentation and coaching staff on GMP and hygiene.
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Technical Trainer
Gilead
United States - Maryland - Frederick
$80k–$104k
21d
Develop and deliver technical training and documentation for manufacturing operations in a biopharmaceutical cell therapy environment.
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Sr Operator - Third Shift
Thermofisher
Fairport, New York, USA
21d
Senior Operator supporting daily manufacturing, filling, packaging, and production activities in a regulated cleanroom environment.
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