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Project Manager / Support (9- 12months)

Ref: JN-102021-198290

Gepostet am 29 October 2021
Job Location

"We believe that the future belongs to those who drive innovation, who shape change and who network through collaboration."

Main Tasks

  • PM Role to Support the SGIE CQV Program Execution Lead
  • Organizing meetings with the different Sites
  • Preparing the Meeting also for others and provides Meetings notes
  • Leading and / or supporting meetings
  • Monitor and Tracks project Activities
  • Execution of related tasks
  • Creates Documents if needed in proper and fast manner
  • Route Documents for Approval in DMS
  • Monitors The Kneat Training
  • Serves the Sites (US, Europe, Asia) and Projects as liaison

Your Profile

  • High Technical Degree
  • Proven Experience in Project Management / Support
  • Experience in Commissioning, Qualification and Validation incl. CSV. Familiarity with biologics (mammalian, CGT) as well as chemical manufacturing technologies desirable.
  • Significant experience in regulated pharmaceutical industry and/or engineering company (DI, GDP)
  • Knowledge of ISPE and ASTM guidelines.
  • Very experienced I technical writing Knowledge and Skills
  • Solid collaboration and influencing skills and the ability to work together with teams and individuals in a highly matrix environment.
  • Language: Excellent command of English and proven knowledge in German necessary (read and write) and other desirable.
  • Experience at working both independently and in a team-oriented environment.
  • Ability to effectively prioritize and execute tasks in a fast-paced environment.
  • Strong written and oral communication skills.
  • Good documentation skills – Create/ review / update GROUP, SOPs, WI (including supporting CSV-Lead, CQV Americas, CQV EMEA / Asia, and Program Execution Lead)
  • Good communication skills – Can lead meetings, organize meetings with other sites - Good problem solving skills – Able to analyze a situation, highlight the challenges and propose solutions in his area of responsibility
  • Admin skills – Grant access to people in Kneat system, organize trainings
  • Good technical knowledge in pharma industry- understands processes, etc. - Will be trained as PU

Thanks you. We are looking forward to your applications.