Job Title:
Quality Manager Investigational Medicinal Products (IMP)
Overview
We are seeking a motivated and reliable Quality Manager to oversee the manufacture and analysis of Investigational Medicinal Products (IMPs). As a delegate of the Swiss Regulatory Authority, you will be responsible for ensuring GMP compliance in our facilities.
Responsibilities
* Acts as a delegate of the Swiss RP for IMPs
* Reviews and approves GMP procedures, records, and reports
* Performs self-inspections in GMP plants and laboratories
* Reports directly to the RP and RP deputy
Requirements
* Bachelor or Master Degree in Life Sciences or equivalent
* Minimum 3 years of relevant experience in the pharmaceutical industry
* Experience in a GMP regulated environment
* Knowledge of cGMP and Quality requirements for clinical development stages of biotechnological and/or parenteral IMPS
Desirable Skills
* Proficient contribution to health authority inspections and internal GMP audits
* Excellent planning and organizing skills
* Strong team player with a high level of self-motivation
* Proven ability to work independently and in a team towards results
About This Role
As a Quality Manager, you will be part of a dynamic team that ensures the highest standards of quality in the manufacture and analysis of Investigational Medicinal Products. You will have the opportunity to develop your skills and expertise in a fast-paced environment, working closely with regulatory authorities and other stakeholders.