We are recruiting for a Project Leader for a permanent role in the field of surgical medical devices. The role will involve GMP delivery of products which will be principally focussed on critical care products. You will have a background in working on medical device projects and be able to demonstrate a thorough understanding of the technologies and systems relevant to the medical devices market as well as a current good knowledge of current me...
Job Title: Biochemistry Development Scientist Location: Worthing, West Sussex Life Sciences degree (preferably Biochemistry/immunology) is ESSENTIAL Pharmaceutical Industry experience (potentially sandwich placement) is ESSENTIAL Experience of plate-based Immunoassays is ESSENTIAL Summary The perfect opportunity for a Life Science graduate with some industrial experience and a...
Organisation Description Developing Pharmaceutical Organisation currently gonig through exciting transitions in what has been phenominal growth, are currently looking for a Validation Engineer with extensive cGMP experience. Job Description Varied tasks within Process & Equipment validation relating to packing inspection and filling machines as well process validation ...
Job Description Reed Scientific is currently recruiting for a temp Validation Technician to work a few days a week. This position is responsible for all equipment and process validations as well as day to day tasks. -Work with QA to develop effective and compliant validation protocols -Take responsibility for all validation associated equipment / hardware / software Successful candidate will have hands ...
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Date: 5 days ago
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India,
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Salary not specified
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1 application
Blue chip global pharmaceutical manufacturing company is currently looking for a Commissioning / Start up Programme Manager to work on an OSD Formulation and Packing (primarily wet granulation) project in India. Project Overview: OSD Formulation and Packing (primarily wet granulation) Bangalore, India All process equipment is of Indian origin Plant capacity - 0.8 Billion tablets Capital cost $25M USD <br...
Job Title: Biochemistry Development Scientist Location: Worthing, West Sussex Biochemistry degree (or similar, such as Microbiology) is ESSENTIAL Some industrial experience (ideally Pharmaceutical) is ESSENTIAL Experience of ELISAs and other plate-based Immunoassays is ESSENTIAL Salary up to £23,000 + Benefits Summary The perfect opportunity for a Life Science ...
Due to expansion there is now a vacancy for a QA / Quality Assurance Specialist with Validation to join a global-leading pharmaceutical company. Salary package for the QA / Quality Assurance Specialist with Validation is c£40,000 + pension + healthcare + life assurance. QA / Quality Assurance Specialist with Validation will be based in Oxford, Oxfordshire. Overview of ...
Location; South-East, UK Salary; Attractive Job Summary and Responsibilities My client is a leader in biotechnology that discovers, develops, manufactures, and delivers innovative human therapeutics. They are currently expanding and have requirements for professionals to join their quality department. They now require a permanent QA Validation Engineer to underta...
Due to expansion there is now a vacancy for a Process Validation QA / Quality Assurance Specialist to join a global-leading pharmaceutical company. Salary package for the Process Validation QA / Quality Assurance Specialist is c£40,000 + pension + healthcare + life assurance. Process Validation QA / Quality Assurance Specialist will be based in Oxford, Oxfordshire. Ove...
Technical QA Specialist GMP FMEA CPK (Good Manufacturing Process),Quality Systems Pharmaceutical Medical Devices oxfordshire 45k Urgent The ideal candidate needs to understand the science involved in the development/ validation of products and processes. Essential Skills. HND/ degree Worked in QA with hands on experience of GMP,(Good Manufacturing Process),Quality Systems Wo...
Validation Manager - based in Glasgow will require relocation Glasgow £Depending on experience Successful international company has an opportunity for a Validation Manager to lead their busy Site Validation team. As Validation Manager you will lead all aspects of the engineering validation program: defining standards for validation compliance objectives; implementing the necessary standards in line with regul...
Due to expansion there is now a vacancy for a Process Validation QA / Quality Assurance Specialist to join a global-leading pharmaceutical company. Salary package for the Process Validation QA / Quality Assurance Specialist is c£40,000 + pension + healthcare + life assurance. Process Validation QA / Quality Assurance Specialist will be based in Oxford, Oxfordshire. Ove...
Due to expansion there is now a vacancy for a Quality Assurance Executive / QA Specialist to join a global-leading pharmaceutical company. Salary package for the Quality Assurance Executive / QA Specialist is c£40,000 + pension + healthcare + life assurance. Quality Assurance Executive / QA Specialist will be based in Oxford, Oxfordshire. Overview of Main Job Functions: "...
Due to expansion there is now a vacancy for a Process Validation QA / Quality Assurance Specialist to join a global-leading pharmaceutical company. Salary package for the Process Validation QA / Quality Assurance Specialist is c£40,000 + pension + healthcare + life assurance. Process Validation QA / Quality Assurance Specialist will be based in Oxford, Oxfordshire. Ove...
Organisation Description Reed Scientific are currently recruiting a Regulatory Specialist, to support validation activities associated with the delivery of product transfer project work. The roles will be part of a team supporting site transfer projects from one facility to another and are intended to be for a fixed 2 year period with flexibility to extend the contract. Job Description <br /...
Validation Manager Glasgow £Depending on experience Successful international company has an opportunity for a Validation Manager to lead their busy Site Validation team. As Validation Manager you will lead all aspects of the engineering validation program: defining standards for validation compliance objectives; implementing the necessary standards in line with regulatory obligations; and engaging with operat...
