Contracting – Brabant Wallon
QA Officer
Description de la fonction
You will ensure the follow-up of productions; this involves monitoring chemical synthesis operations through dossier review, managing deviations, and following change control (review of change control).
Daily contact with production is required.
Profil
- Bachelor’s degree in Sciences
- Minimum 3-5 years of experience in Quality Assurance in a regulated pharmaceutical environment or other life science or health-related field.
- Experience in pharma is a must (must quickly become autonomous): experience with chemical/pharmaceutical production, development, and/or regulatory requirements, including knowledge of production best practices in the pharmaceutical industry.
- Experience in manufacturing batch record QA review and deviation QA review is a must.
- Experience with Quality Management System.
- Good documentation practices.
- Ability to challenge partners.
- Fluency in French and English
Offre
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV,
Afficher l'adresse e-maillena.palmeri@jeffersonwells.be