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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: Switzerland

Are you passionate about quality and precision? Join our client as a dedicated Quality Manager and help ensure top-tier standards every day.

91��ɫ is seeking an IMP Quality Manager to ensure that all investigational medicinal products meet quality standards and comply with regulations. You will work closely with manufacturing units and clinical packaging teams to maintain high-quality operations. This position requires flexibility, strong communication skills, and a deep understanding of Good Manufacturing Practices (GMP).

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

Act as a representative for quality assurance in the production of investigational medicines.
Ensure compliance with GMP standards for manufacturing and testing processes.
Review and approve quality procedures and reports.
Conduct inspections in manufacturing plants and labs.
Report directly to the quality assurance leadership team.

Key Skills and Requirements:

Degree in Life Sciences or a related field.
Experience in the pharmaceutical industry and GMP environments.
Familiarity with manufacturing and quality control of sterile products.
Strong knowledge of GMP and quality requirements for clinical development.
Proficient in English and German communication.
Ability to work independently and collaboratively, with strong problem-solving skills.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

91��ɫ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. 91��ɫ is acting as an Employment Agency in relation to this vacancy.

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