Clinical Manager Analytical Development and Quality

Vor 6 Tagen

Allschwil, Schweiz Source Group International Vollzeit

In this role you will be dealing with the analytical development of Drug Products and Drug Substances. You will need to ensure that all products are delivered according to the standards required by regulatory guidelines and GMP.

**Responsibilities**:

- Manage a team of up to 3 employees as well as the GMP laboratory
- Responsible for 4 projects
- Organisation of lab activities according to SOP’s.
- Ensure maintenance and operation of analytical equipment in accordance to GMP.
- Write-up reviews and documentation of analytical activities.

**Requirements**:

- College, or university degree or equivalent education in the field of chemistry, biochemistry, pharmacy, biology or chemical engineering
- In addition to knowledge of the GMP/regulatory requirements, a strong background in analytical chemistry is required.
- Proficient in English.
- Broad knowledge in analytical chemistry.
- Ability to manage a team

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