Descripción del puesto:
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 Analytical documentation relating to analysis of oral solid dose Bulk tablets. - Assist in Preparation of documentation for QC Testing (Analytical Methods, Release specifications, Analytical Worksheets etc). - Investigating and close out of Laboratory Incident reports (LIR's) - Carrying out & Assisting in Root Cause Problem Solving (RCPS) sessions in response to Right First Time issues. Identifying and implementing corrective and preventative actions from RCPS. - Participate in, and lead, relevant Quality Risk Management Assessments - Being involved in the continuous improvements of Quality Control Systems, working with the Operational Performance department. - Providing QC support to other departments. - Collaborate with Regulatory Affairs department to develop a central file for all Products used in SII and establishing the relevant release specification requirements. Duration of the mission: 12 months (renewable)
Requerimientos del candidato/a:
Educational background: University/Technical College Specialization: Science/Quality Assurance /Production Field of study: Pharmaceutical or Manufacturing Languages: English Computer skills: MS Office, MS Project
| Origen: | Web de la compañía |
|---|---|
| Publicado: | 28 Oct 2026 (comprobado el 03 Nov 2026) |
| Tipo de oferta: | V.I.E. |
| Duración: | 12 meses |
| Idiomas: | Inglés |