Project Coordinator GMP

Vor 2 Tagen


Visp, Schweiz Actalent Vollzeit

Direct message the job poster from Actalent

Life Science Recruiter, specialised in Scientific

We are seeking a highly motivated and detail-oriented Project Scheduler to join our client's team in a biopharmaceutical environment in Visp (Switzerland). The role will support a project involving mechanical adaptations and operational improvements in an existing mammalian commercial production line. The Scheduler will be responsible for developing, maintaining, and coordinating project schedules, ensuring alignment between engineering, operational, and compliance activities.

Key Responsibilities:

  • Develop and maintain a comprehensive project schedule from conceptual design to performance qualification (PQ), capturing both mechanical adaptations and operational improvements.
  • Integrate Engineering, Procurement, Construction Management (EPCM) timelines with operational and compliance-driven activities.
  • Monitor progress against the schedule, identify potential risks or delays, and propose corrective actions to maintain project timelines.
  • Collaborate with QA/QC teams to ensure all operational activities meet GMP requirements and are completed on schedule.
  • Utilize project management software (e.g., Primavera P6, MS Project, or equivalent) to build and manage schedules.
  • Ensure that compliance-related activities such as TCRs, CRs, and PQ are well integrated into the schedule.

Requirements:

  • Bachelor’s degree in engineering, Life Sciences, Project Management, or a related field.
  • Minimum 3-5 years of experience in scheduling within a regulated (GMP) environment, preferably in the pharmaceutical or biopharmaceutical industry.
  • Proficiency in project scheduling tools (e.g., Primavera P6, MS Project).
  • Strong understanding of GMP compliance, including change management (TCRs, CRs) and validation activities (IQ/OQ/PQ).
  • Familiarity with biopharmaceutical manufacturing processes, particularly mammalian production systems, is a plus.

Duration: until 31/12/2025

If you are interested please apply directly, or send me your CV at cpflieger@actalentservices.com.

Seniority level
  • Associate
Employment type
  • Contract
Job function
  • Manufacturing and Project Management
  • Pharmaceutical Manufacturing and Biotechnology Research
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