To manage documentation at Thames Valley Science Park, Reading, in support of Micregen’s operations relating to manufacture, testing, R&D and clinical trial activities. Responsibilities- To maintain the Pharmaceutical Quality System (PQS) for Micregen Ltd. To manage and control documents in compliance with EU Good Manufacturing Practice (GMP) guidelines. To act as Deputy Archivist for GMP documents, providing assistance to the Archivist with compilation, checking, indexing and archiving documents. To assist Micregen staff with the writing of PQS documentation, performing such activities as editing and updating documents under the direction of Micregen staff. To provide administration support to the Micregen personnel and visitors at TSVP in areas such as managing personal schedules, arranging meetings and co-ordinating travel, insurance, accommodation, course booking, catering and telephone arrangements. Minimum Requirements- 5 years’ experience in a similar role.

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