Gmp jobs in Cambridge

Job Title: Validation Engineer. The Validation Engineer needs to provide Validation leadership, Specialist Knowledge and Executes validation projects, ensuring these are completed in line with GMP requirements, industry standards, company procedures and business requirements, collaborating with k...

Job Title: Senior Analytical Chemist Location: Cambridge (Lab Based) Job type: 24-Months Fixed Term Contract At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our par...

Job Title: Principal Chemical Analyst Location: Cambridge (Lab Based) Job type: 24-Months Fixed Term Contract At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our pa...

Job Title: Principal Chemical Analyst Location: Cambridge (Lab Based) Job type: 24-Months Fixed Term Contract At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our pa...

Job Title: Senior Analytical Chemist Location: Cambridge (Lab Based) Job type: 24-Months Fixed Term Contract At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our par...

CK Group are recruiting for a Head of Production on behalf of a growing Cell Therapy CDMO to lead a manufacturing team and oversee production activities. This role will be based at their site in Cambridge on a permanent basis. The Role: This is a key role where you will be leading the manufacturi...

If you are an experienced QA professional within the biotech GMP sector with prior line management experience, this may be an opportunity of interest. The Opportunity This is an opportunity for ...

The company is growing rapidly and is establishing a GMP gene synthesis hub at its site just north of Cambridge, UK to facilitate the scaling and optimisation of a proprietary DNA manufacturing ...

This will include ensuring activities associated with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements ...

As the Senior Quality Assurance Specialist, you will be responsible for executing QA tasks to ensure compliance with local GMP facility processes during manufacturing and testing activities. Your ...

Good Manufacturing Process (GMP) audits of process, people and work in process product. * Carry out Internal audits against a defined sched... ZIPC1_UKTJ

Significant industrial experience working in or maintaining a GMP/GLP compliant analytical environment. * Experience with EU regulatory guidelines, quality management systems and quality risk ...

They will assist software development within the team, ensuring best practices to medical device and GMP standards where appropriate. The software engineer at MFX will be a key player in advancing ...

The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition ...

Microbiological analysis, including method and process validation within a Pharma/Biotechnology/ATMP GMP laboratory. [E] Detailed understanding of the assay or test principles, including ...

Significant industrial experience working in or maintaining a GMP/GLP compliant analytical environment. * Experience with EU regulatory guidelines, quality management systems and quality risk ...

Maintain accurate documentation and adhere to Good Manufacturing Practise (GMP) standards. * Conduct pre-use checks on mechanical handling equipment (MHE) to ensure safe operation. * Embrace a ...

Maintain accurate paperwork and adhere to Good Manufacturing Practise (GMP) standards and clean-as-you-go policy. * Conduct checks on mechanical handling equipment (MHE) to ensure safe operation

Chemistry, production operator, process operator, chemical operator, plant operator, GMP, manufacturing

Follow all relevant medical device directives and EU GMP Annex 11. Technical skills needed include: * 2 years in a regulated industry or similar, * 2 years of experience with writing code in C/C++ OR ...

Maintain accurate and audit-worthy paperwork, adhering to Good Manufacturing Practise (GMP) standards and clean-as-you-go policy. * Conduct mechanical handling equipment (MHE) checks prior to use ...

Working as a support function to operations to ensure hygiene levels of the facility are maintained by conducting GMP / Glass and Hard Plastic and Fabrication audits in conjunction with departments ...

ISO9001 experience preferred, GLP/GMP also advantageous. * Confident presenting KPIs and other updates at weekly team meetings. * Microsoft Word, Excel, and PowerPoint are essential. * Takes pride in ...

GMP knowledge coupled with proven experience of analytical method validation & transfer principles. What we offer * Competitive hourly rate and retention bonus * Training & development * A quick ...