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Project Manager QA (f/m/d)

The Swiss based Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of pepTides and oligonucleoTides. As a full service provider Bachem offers products for clinical development and commercial applications as well as a comprehensive catalog and exclusive custom synthesis. With 50 years of experience and subsidiaries in Switzerland, the United States, the United Kingdom and Japan, Bachem is the partner of choice for the biotech and pharma industry worldwide.  
Bachem. Leading Partner in Tides 

In order to continue our organic growth, we are constantly looking for talent.

Your responsibilities

 

We are looking for a well-organized and highly motivated Project Manager for our QA. In this position you will be responsible to support NCE-, generic- and company projects regarding all quality related topics. This encompasses the definition of a control strategy and general project life cycle strategy in early GMP development, process validation in the later project phase and continuous process verification in the commercial manufacturing phase. In general the QA PM is working to resolve any QA issues that arise during the project life cycle. You are a core project team member, that interacts with multiple departments (e. g. production, R&D, QC, business development and project management), actively coordinates project related work within our QA departments and communicates efficiently with international customers. The responsibility of this function includes also the review and approval of cGMP relevant documents, decision making according to current SOPs as well as review and approval of change controls and deviations.

 

Your qualifications
You have a Master degree or Ph.D. in Chemistry or Pharmacy or an equivalent qualification, experience in CMC development, at least two years of experience in project management within the chemical/pharmaceutical industry and very good cGMP knowledge including sound knowledge of international and national cGMP-, ISO- requirements and other quality assurance guidelines. You work service minded, task-oriented, structured, with excellent organizational skills, very good interpersonal skills including verbal and written communication skills and a very good command of English and German. As a strong team player you provide guidance on GMP related topics and support multiple inter-divisional project teams in QA-related decisions by powerful arguments. You achieve suitable and acceptable solutions with an open minded, cooperative ability and good negotiating skills.

 

We offer
We offer an exciting and challenging job in a dynamic and growing environment which guarantees diversity and personal advancement. In this position, you have the opportunity to influence the entire development cycle of the respective API.

 

Are you interested? Please submit your application with full supporting documents online to Mrs. Fabienne Carabelli (Human Resources). We only consider direct applications.