In this position you will lead and oversee analytical development and quality control activities. You will be responsible for ensuring GMP compliance and fulfilling regulatory requirements in the QC department and provide guidance in developing UHPLC based analytical methods. Furthermore, you will contribute your expertise in drug product quality to cross-functional pharmaceutical development project groups. With a diverse range of tasks and close collaboration with other departments, you will gain valuable insights and expertise across various areas in a short period of time.
Your job profile includes:
Responsibility for a small team and organization of the department and laboratory
Responsibility for drug product quality and stability studies
Ensuring proper development and validation of analytical methods
Managing equipment qualification, maintenance and calibration
Active involvement in interdepartmental projects (e.g. with regulatory, production, quality assurance)
Change control, deviation and CAPA management, OOS investigations
As prerequisites for this exciting and challenging job, we expect a university degree in a relevant field (such as biochemistry, chemistry, or pharmacy) and at least 4 years of hands-on experience in a GMP-regulated environment. You bring strong interpersonal skills and experience in successfully leading a small team. Your analytical mindset allows you to stay focused and maintain clarity even in hectic situations. As part of a dynamic start-up, you will be involved in a wide range of responsibilities - so flexibility, initiative, and a hands-on attitude are essential. You are fluent in English; knowledge of German or French is a plus.
Interested candidates are kindly requested to send their full application to Ms. Noëlle Haas, who can also be contacted for additional information by phone () or e-mail ().
jidf7f7c48a jit0624a jiy25a