Project Manager CMC/Regulatory

Beschreibung

Memo Therapeutics AG is a clinical stage biotech company developing antibody-based therapies in the area of infectious diseases and cancer.
With currently two programs in clinical development and a well-filled pipeline of therapeutic antibodies we are seeking a Project Manager.Planning and management of

• Manufacture and quality control of investigational medicinal products
  • Nonclinical studies
  • National and international regulatory interactions
  • Project budget and resources
• Plan and facilitate pharmaceutical development of innovative medicines from bench to market
• Review and evaluation of project proposals
• National and international teamwork and close collaboration with vendors and partners
• Reporting to the Chief Development Officer (CDO)

• >4 years of project management experience in pharmaceutical R&D, preferably with experience in CMC
• Scientific background: MSc, preferably PhD, in life sciences, chemistry or pharmacy
• Excellent self-organization skills
• Flexibility and ability to work pro-actively
• Ability to comprehend and oversee complex projects and prioritize required actions
• Excellent written and spoken English language skills
• Applicants must be EU / EFTA citizens or have a valid work permit for Switzerland

Memo Therapeutics AG offers excellent career opportunities in a fast growing biotech company in state-of-the-art facilities at the Biotechnopark Schlieren, Zurich.

Please send your application (short cover letter + CV) in one pdf document to [Click Here to Email Your Resumé]