Description
Leading French independent pharmaceutical Company, specialised in ethical medicinal products. 92% of Servier’s sales are achieved internationally, with several subsidiary companies abroad. We are looking for V.I.E’s, for our subsidiary in Ireland.
Description of the mission:
- Carrying out the review of batch manufacturing documentation relating to oral solid dose production
- Preparing documentation for QP release in a timely manner
- Investigating and close out of deviations while working in close co-operation with other departments
- Identifying and implementing corrective and preventative actions
- Participate in, and lead, relevant Quality Risk Management Assessments
- Participating in internal and external audits as required
- Being involved in the continuous improvements of Quality Systems
- Providing QA support to other departments.