Project Director

Vor 2 Tagen

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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