QUALITY CONTROL GMP jobs in CAMBRIDGE MA, United Kingdom

quality support for continuous improvement of Artwork version control, Bill of Materials and change management. Support the...Job Description GENERAL/POSITION SUMMARY The Quality Manager is responsible for managing multiple department...

Vertex Pharmaceuticals

Job Description General Summary: The GMP Operational Quality Senior Specialist Cell and Gene supports the... principles and application of quality assurance and regulatory compliance. The incumbent supports or executes a wide...

Vertex Pharmaceuticals

Job Description General Position Summary: The GMP Quality Operations Director serves as a Quality leader in the..., implementation, and maintenance of relevant quality initiatives in support of their function. The leader is adept at troubleshooting...

Vertex Pharmaceuticals

sanitization. Collaborate with Manufacturing, GMP Operations Manager, and Quality teams to manage schedules necessary to sanitize...Job Title GMP Cleaner Job Description Summary This position requires strict adherence to current Good Manufacturing...

Cushman & Wakefield

sanitization. Collaborate with Manufacturing, GMP Operations Manager, and Quality teams to manage schedules necessary to sanitize...Job Title GMP Cleaner Job Description Summary This position requires strict adherence to current Good Manufacturing...

Cushman & Wakefield

Job Description The Manager, Quality Control provides oversight of a variety of analytical functions that occur in..., cell-based assays, ELISA, and applying/interpretation of GMP requirements Effective communication skills, both verbal...

Vertex Pharmaceuticals

such as training, documentation and change control. The role will support external vendor quality activities as applicable. The... experience such as manufacturing, quality assurance, and/or quality control in biotechnology/regulated pharmaceutical environment...

Vertex Pharmaceuticals

for identifying risks and communicating gaps to GMP process/systems. Participate in the change control review meeting... audits and inspections, and serve as quality subject matter expert (SME) for facility control programs and the validation...

Vertex Pharmaceuticals

for ensuring that the quality of product meets GMP standards, Biogen standards, ISO 13485, and ISO 14971 specifications... Quality System Regulations and ISO 13485 design control (21 CFR 820.30) and risk management (ISO 14971) requirements. Lead...

Biogen

Job Description General Summary: The Sr. Specialist GMP QA Operations works with a high degree of independence..., while providing oversight of the development, implementation and maintenance of relevant quality initiatives in support...

Vertex Pharmaceuticals

- functional quality systems Conducts GMP document review, including procedures, work instructions, specifications, methods...Job Description General Summary: The Senior Manager, Quality Analytical Microbiology is an advanced technical...

Vertex Pharmaceuticals

trial material efforts across four main areas a) GMP review and control for analytical documents b) Release testing... oversight, Stability and Shelf life c) Reference Standard Management d) GMP Quality Systems Contribute to product development...

Takeda

to ensure safety and quality of our products. Within the Molecular & Viral Safety team, the development, validation... Development, Quality and Regulatory partners. Embody FAIR principles (Findable, Accessible, Interoperable, and Reusable...

MSD

streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP... control of your facility and expertise while leveraging available space. About Charles River Charles River is an early...

Charles River Laboratories

, comprehending, and complying with all SOPs and quality assurance standards pertaining to laboratory animals for research... and collect various aseptic sampling for the monitoring of water quality, sanitized animal racks, and equipment. Inspect...

Charles River Laboratories

, quality/analytical control strategy, and specification justification strategy (Mentoring, training and coaching of ADRs... development experience required GMP and compliance experience required Regulatory submission experience required with basic...

Takeda

, United Kingdom. Position Summary Reporting into the Senior Manager, External Quality Control & Stability, the Stability... with Research, Process Development, Quality teams, Regulatory and our CDMOs. Responsibilities Monitor stability program...

CRISPR Therapeutics