Join one of the world’s fastest growing pharmaceutical companies!
You will have the opportunity to thrive in a fast-paced, strategic environment where bold, innovative thinking isn’t just welcomed, it’s encouraged.
Across all functions, we relish the opportunity to help our people fulfill their potential. Our rapid growth strategy means plenty of opportunities to step into the spotlight.
This position is part of the Operational team and reports to the head of quality. She / he is responsible for managing quality aspect related to the operations (production, control, storage and distribution).
Yours responsibilities :
Review / approval of the documentation related to the operations
Review batch records to support release of finished products
Ensure the QA release of raw material and packaging material
Management of deviation, CAPA, OOS, CC, supplier complaints related to the supplier’s complaints in collaboration with the other departments
Actively participate in continuous process improvement
Ensure compliance with GMP and good documentation practices as well as with internal standards (SOP)
Ensure critical topics are adequately and timely escalated to higher management
Performs internal audits, shop-floor visits
Contributes to local and / or transversal improvement projects to ensure the compliance level is maintained
Your profile :
Baccalaureate or Master in Sciences (Biology, Biochemistry, Chemistry, Pharmacy), or equivalent based on professional experience
5 years’ experience as QA in drug manufacturing
Good interpersonal and communication skills
Flexible, solutions oriented, proactive, having an excellent critical and analytical mind and being stress resistant
Fluent in French and in English
Excellent knowledge of MS Office®
Interested? Contact diane.louppe experis.be or 02 389 11 76.
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