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For one of our client, a pharmaceutical companyspecialized in aseptic manufacturing, we are looking for a

Team Leader Compliance PQS
Location: Jura canton
Contract: Permanent

Your Tasks:

• Overseeing a small team within the Quality Assurance department to ensure compliance.
• Managing sub-processes related to deviations, Corrective and Preventative Actions (CAPA), and Change Control.
• Collaborating on investigations and approving investigation reports for minor and major deviations.
• Representing the company in dealings with clients regarding deviations or Change Control.

By fulfilling these responsibilities, you will significantly contribute to the high quality of the services offered by our client.

Your Profile:

To be successful in this role, the following qualifications are required:

• A scientific degree.
• A minimum of 3 years experience in Quality Assurance, including investigations related to deviations, CAPA, and Change Control.
• 5 years of experience in an environment compliant with cGMP standards.
• Fluency in French and English (C1 level) with excellent writing skills.
• Proficient in MS Office and Visio.

Preferred, but not required skills include:

• Experience with eQMS (Trackwise or similar).
• Experience as a QP or QP substitute.
• Experience in regulatory Affairs

For one of our client, a pharmaceutical companyspecialized in aseptic manufacturing, we are looking for a

Team Leader Compliance PQS
Location: Jura canton
Contract: Permanent

Your Tasks:

• Overseeing a small team within the Quality Assurance department to ensure compliance.
• Managing sub-processes related to deviations, Corrective and Preventative Actions (CAPA), and Change Control.
• Collaborating on investigations and approving investigation reports for minor and major deviations.
• Representing the company in dealings with clients regarding deviations or Change Control.

By fulfilling these responsibilities, you will significantly contribute to the high quality of the services offered by our client.

Your Profile:

To be successful in this role, the following qualifications are required:

• A scientific degree.
• A minimum of 3 years experience in Quality Assurance, including investigations related to deviations, CAPA, and Change Control.
• 5 years of experience in an environment compliant with cGMP standards.
• Fluency in French and English (C1 level) with excellent writing skills.
• Proficient in MS Office and Visio.

Preferred, but not required skills include:

• Experience with eQMS (Trackwise or similar).
• Experience as a QP or QP substitute.
• Experience in regulatory Affairs