Quality Assurance Specialist – Raw Material
Infos sur l'emploi
- Date de publication :08 janvier 2025
- Taux d'activité :100%
- Type de contrat :Temporaire
- Lieu de travail :Vaud
We are looking for a Quality Assurance Specialist – Raw Material or a temporary assignment, initially until the end of February, for one of our prestigious clients.
Join the QA team to oversee quality activities related to raw material batch review and release while ensuring compliance with regulatory requirements in a pharmaceutical environment. This key role ensures adherence to GMP standards and specifications.
Main Responsibilities:
- Collect, review, and complete all documentation required for raw material batch review and disposition.
- Provide quality oversight for all quality events (e.g., deviations, investigations, CAPA, change control) within the area of responsibility.
- Act in compliance with legal and regulatory requirements as well as company guidelines.
Your Profile:
- At least 2 years of experience in realising of raw material in the pharmaceutical industry.
- Strong knowledge of cGMP, cGDP, and global regulatory requirements related to pharmaceutical manufacturing and testing.
- Fluency in French and English is mandatory.
Interested? We invite you to submit your application confidentially.
Contact
- Morgane CayuelaÉcrire un email
