Project Director CQV

vor 3 Wochen


Basel, Schweiz Callista Vollzeit

For a Top 10 pharmaceutical company in Switzerland we are recruiting this very exciting career opportunity The role of a Project Director - CQV:

  • Provide cGMP leadership and guidance for the integration and delivery of CQV services for our Life Sciences clients.
  • Managing mid-sized to large projects related to process equipment and clean utilities including start-up and commissioning
  • Lead design review, site acceptance and installation of equipment
  • Support onsite and offsite activities, such as: FATs, SATs, Executions and System Walkdowns
  • Management of any aspect of C & Q, verification as requested i.e., Change Controls, Management of Contractors and Vendors, document control, punch list management.
  • Allocate project resources for efficient execution of project deliverables.
  • Deliver the C&Q activities as required to meet the schedule
  • Track progress of C&Q activities as required.
  • Coordinate support during C&Q execution


Position Requirements
Minimum MS in a relevant science or engineering field, or equivalent

  • 15 + years of Commissioning, Qualification, Validation and Compliance experience in the Life Sciences or Regulated Industries; Sound technical knowledge of EU and global regulatory requirements. Proficient in cGMP standards.
  • Experience in collaborating and managing Commissioning, Qualification and Validation deliverables for one or Multiple Projects
  • Skilled at planning and tracking project activities and schedules
  • Excellent interpersonal skills to form strong relationships with internal and external clients
  • Excellent oral and written communication skills
  • Excellent problem-solving skills
  • Customer-service focused.
  • Proficient in life science manufacturing processes in areas such as biotech, aseptic fill/finish, OSD, Gene Therapy or equivalent experience.
  • Able to travel domestically and internationally if required.


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