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QC Project Manager

Il y a 2 mois


Toulouse, Occitanie, France Optimus Life Sciences Temps plein
About the Role

We are seeking an experienced QC Project Manager to lead a critical Quality Control (QC) Stream for a major biotechnology project in Toulouse. As a key member of our team, you will be responsible for managing the qualification and validation of cutting-edge laboratory and analytical equipment, ensuring compliance with regulatory standards (GMP, BPF, FDA).

Key Responsibilities
  • Lead the qualification and validation of laboratory and analytical equipment, including mass spectrophotometers, electron microscopes, centrifuges, and endotoxin analyzers.
  • Manage the end-to-end project lifecycle, from planning to execution, ensuring compliance with IQ/OQ/PQ protocols.
  • Develop and maintain detailed project schedules using tools like MS Project.
  • Coordinate and lead project committee meetings, tracking progress and deliverables to meet contractual commitments.
  • Manage risks, issues, and scope changes, ensuring customer satisfaction throughout the project.
  • Oversee and mentor a team of consultants involved in the QC stream.
  • Collaborate with the client's QC and QA departments, ensuring timely and compliant project delivery.
  • Participate in the recruitment and onboarding of additional project resources as needed.
Requirements
  • 8-15 years of experience in project management within the life sciences, biotechnology, or pharmaceutical industries.
  • 2-3 years of hands-on experience with laboratory equipment qualification and validation (IQ/OQ/PQ).
  • Strong understanding of GMP, BPF, and FDA compliance requirements.
  • Proven leadership skills with the ability to manage multidisciplinary teams.
  • Strong communication skills, both written and verbal, with the ability to build effective client relationships.
  • Fluency in English is essential; French is a big plus.