On-Site Validation Engineer (GMP) – Pharma Manufacturing

PQE Group; Lure; Sur place; EUR 40 000 - 55 000; Plein temps

Résumé du poste

A leading pharmaceutical company is seeking a Validation Engineer for a 3-month renewable contract in Lure, France. The successful candidate will track validation plans and conduct risk analyses, ensuring compliance with Good Manufacturing Practices and French regulations. Strong communication and collaboration skills are essential. This on-site role may allow for occasional remote work but requires flexibility in hours due to operational needs. Experience in pharmaceutical manufacturing is preferred.

Qualifications

• This role requires previous experience in process validation in pharmaceutical manufacturing.
• Must have familiarity with French regulations related to validation.
• Ability to work independently on tasks assigned.

Responsabilités

• Track and report on the master validation plan progress.
• Conduct process risk analyses and draft validation documents.
• Plan and manage testing activities and monitor production.
• Propose corrective action plans for any non-conformities.

Connaissances

Process validation

Communication skills

Collaboration

Good Manufacturing Practices (GMP)

Formation

Engineering degree or equivalent

Description du poste

A leading pharmaceutical company is seeking a Validation Engineer for a 3-month renewable contract in Lure, France. The successful candidate will track validation plans and conduct risk analyses, ensuring compliance with Good Manufacturing Practices and French regulations. Strong communication and collaboration skills are essential. This on-site role may allow for occasional remote work but requires flexibility in hours due to operational needs. Experience in pharmaceutical manufacturing is preferred.