Validation Engineer - Cambridge - 6 Month Contract

i Pharm Consulting Ltd
05 Oct 2017
02 Nov 2017
Contract Type
Full Time
Validation Engineer - Cambridge - 6 Month Contract Validation Engineer required for a leading Pharmaceutical company to work a 6 month initial contract. You will support the engineering and manufacturing functions in the review and approval of validation documentation to meet cGMP requirements by providing expert support in risk management, protocol preparation and execution and acting as the quality approval authority for validation. Applicants must be eligible to work within the UK. JOB TITLE Validation Engineer / Quality Engineer / QA Engineer LOCATION UK / England / Cambridge LENGTH 6 Months initially ROLE/DESCRIPTION -Provides validation change impact assessments -Responsible for the issue of the Validation master plan -Ensures all requalifications are executed against schedule -Work closely with manufacturing and engineering to deliver process improvements -Identify process control improvements and compliance risk improvements -Provide input to the specification, development and installation of process equipment -Support the development and implementation of quality plans -Is QA approval authority for Validation protocols and reports -Work as part of the larger compounding network to ensure changes, improvements and best practice REQUIREMENTS -Degree in Engineering, Chemistry, Biochemistry or Biology or several years of Validation Engineering experience -Ability to write protocol reports for validation or trial purposes -Up to date knowledge of regulations -Knowledge of drug or device regulations, including 21CFR Part 11 / ISO13485 -Experience of aseptic manufacturing -Training in GMP ABOUT i-PHARM CONSULTING i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics. [URL removed] TO APPLY If you would like to discuss this vacancy further, please call Recruitment Consultant David Fearnley on [Phone number removed] or email [Email address removed]. If this role is not suitable, David is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
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