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 a variety of crossfunctional pharmaceutical development project groups. This position requires a strong technical background, a pragmatic and forward-thinking approach to problem-solving and a strong quality mindset.
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 (e.g. biochemistry, chemistry, pharmacy). Existing practical work experience in a GMP environment of at least 5 years is required. You have excellent interpersonal skills and experience in leading a small team. You are an analytical thinker and maintain the overview even in hectic situations. You show initiative and entrepreneurial spirit and are excited to participate in the dynamics of an innovative start-up company. You are fluent in English and knowledge of German or French is beneficial.
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 ().
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