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Gmp compliance

Wavre
Pauwels Consulting
Publiée le 30 janvier
Description de l'offre

Join a cutting-edge environment where your contributions will play a vital role in advancing quality assurance in the
pharmaceutical industry
. This position offers the opportunity to engage with a dynamic team committed to excellence and compliance.

We are looking for a dedicated
QA Compliance
professional who is eager to utilize their expertise to support operational efficiency and compliance with the highest standards. If you have a solid background in quality assurance and thrive in a collaborative setting, this role is designed for you.

* You ensure accountability for all main quality activities linked to Contract Manufacturer Operations (CMO) management.
* You provide support for product batch release activities.
* You ensure the review and approval of product market complaints.
* You evaluate deviations and oversee corrective and preventive actions (CAPA) closure.
* You manage changes control within quality operations.
* You maintain effective communication with various operational departments to uphold quality standards.
* You generate and analyze compliance metrics to drive continuous improvement initiatives.

What are we looking for?

* You hold a university certificate with scientific orientation, such as in Bioengineering, Biology, Biotechnology, Pharmacology, or Chemistry.
* You have at least
5 years of experience
in a cGMP environment.
* You possess solid knowledge of regulatory matters and Good Manufacturing Practices (GMP).
* You bring strong analytical and critical thinking skills with a problem-solving mindset.
* You are an effective communicator with strong networking and influence skills to work within a QA and IT matrix organization.
* You demonstrate excellent technical writing abilities.
* You are proficient in
English
(oral and written).

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