Project Manager in CDMO - Fluent German speakers

€60000 - €65000 per annum
Sep 23, 2020
Oct 23, 2020
TC 250277 16
Triada Chalkidou
Organization Type
Contract Type
Full Time

My client is a is an international service company (CDMO - Contract Development Manufacturing Organization) for the biopharmaceutical industry and they are leaders when it comes to biologics development platforms and flexible GMP manufacturing services.

Now, they are looking for a Project Manager in their site in Heidelberg to join their team.

So what's in it for you? Permanent full-time employment, flexible working hours, friendly working environment and a lot more!

Your area of ​​responsibility:

  • Management of customer projects with responsibility for time and budget
  • Responsibility for the coordination of internal resources and external service providers
  • Planning projects together with operations
  • Single point of contact for customers and external partners within your projects
  • Responsible for communication between the various stakeholders and for information about the status of the projects
  • Definition and tracking of project milestones together with the key stakeholders (customers, management, departments, external partners)
  • Identification of project risks and implementation of suitable solution strategies
  • Responsibility for project controlling and for reporting the progress of the project
  • Creation of presentations and reports
  • Compilation of regulatory-compliant documentation for the various clinical phases (CTD part IMPD)
  • Support of sales in the creation of offers as well as project cost calculation
  • Implementation and support of internal projects
  • Your qualifications & skills

  • Completed degree (diploma / MSc / PhD) in the field of biology, biochemistry, biotechnology, pharmacy or a related discipline
  • First project management experience in the biopharmaceutical field desirable
  • Knowledge in the area of ​​CMC regulatory affairs of high-molecular proteins such as monoclonal antibodies (NBE and biosimilars) is desirable
  • Experience in the context of regulatory requirements of late-stage projects (clinical phase 3 and approval) desirable for worldwide approvals
  • Experience in at least one specialist area (e.g. cell line development, USP, DSP, analytics) in the development and production of biopharmaceuticals
  • Fluent knowledge of the English language and very good knowledge of German
  • Excellent communication skills, strategic thinking and solution orientation
  • If this sounds like the right opportunity for you, please apply here or send your CV to me in word format, on or call me directly on +49 892 109 3363 for a confidential conversation.

    Or, if this does not sound like the right role for you, but you are in the pharmaceutical industry please feel free to get in touch with me to find out about other relevant opportunities we may have.