Working alone or in teams directly for clients or on EPCmV projects, the incumbent`s key responsibility is to ensure that equipment/utility systems are qualified in line with client/regulatory body expectations with respect to the original cost and timeline estimates. Assignments will typically include all phases of qualification (design, installation, operational, performance qualifications) and may include process-related validation.
The technical base will mainly cover equipment systems validation in the pharmaceutical or biotech industries. Some experience of computer system validation in accordance with GAMP would be advantageous.
Qualifications:
Life Science or Engineering Degree. Corporate member of relevant institution.
Experience:
5 years` equipment/ process validation experience in the pharmaceutical or biotech industries with some supervisory experience in a related field.
Skills/Knowledge:
Good Knowledge of qualification, GMP and legislative requirements.
Extensive equipment, utility, process start up and validation knowledge.
Scientific report/protocol writing skills.
Presentation skills.
Time Management. | 
Contact
Darren Acton
 on 08712 770 851 |
