We are looking for a QA Supplier Engineer one of our prestigious client, to be responsible for the management of all supplier at pharmaceutical manufacturing site, in the canton of Vaud.
Join a dynamic global team, to which you will make a lasting contribution as an SME for continuous improvment.
Responsibilities :
* Coordinate daily quality assurance activities related to Supplier Management, such as supplier qualification, performance monitoring, audits, handling change notifications...
* Draft, review, and approve necessary documentation to maintain compliance with cGMP.
* Oversee the Supplier Audit program, including evaluation, approval, and continuous monitoring.
* Ensure timely execution of supplier audits as per the scheduled plan.
* Conduct supplier audits when required.
* Create and maintain documented procedures for managing suppliers.
* Handle, review, and approve deviations, investigations, and CAPA plans.
* Evaluate and authorize changes for implementation.
* Manage and update the supplier and material list within the QMS system.
* Support inspections by health authorities (e.g., Swissmedic, FDA, and other international regulatory bodies) within your area of expertise.
Your profile :
* Degree in sciences (such as pharmacy or biotechnology for example).
* At least 5 years' experience in Quality Assurance roles within the pharmaceutical industry including supplier management and supplier audits.
* Strong knowledge of GMP.
* Fluent in French and English.
For more information, please feel free to contact Morgane CAYUELA at morgane.cayuela@axepta.com
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Anstellungsart: Festanstellung