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Gmp Compliance
il y a 1 semaine
Location:
Wavre
- Type:
Contracting
#20811
GMP Compliance
Brabant Wallon - contracting
Our partner is looking for a
GMP Compliance to join its team. This international company is well-known for its pharmaceuticals products.
What are your responsibilities?
The purpose of the role is to support the operation QA team to assure and maintain the organization of the activities linked to the quality oversight of the manufacturing activities by:
- Supporting the compliance authority for change controls linked to HPV restart
- Following up of the planification and execution of SOP reviews linked to CAPA implementation
- Assuring quality oversight for the planification of HPV production (day to day questions )
- Writer role for sterility assurance topics: Risk assessment environmental monitoring (EM), review PQ EM, review EM SOPs
- Identifying, developing and Implementing improvements to the quality oversight processes for HPV restart
Who are you?
- You hold a University degree: master degree in Sciences or Engineering
- You have at least 5 years experience in the Pharmaceutical/Biotech industry with significant experience of GMP
- You are open minded, determined, curious, well organized, rigorous and sociable
- You speak French and English
What can you expect?
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.
You're interested in this job? We kindly invite you to apply.
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