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Production Supervisor - GMP

September 5th 2019

MaSTherCell, the global cell and gene therapy CDMO partner

Mission Description

  • Manages established GMP production process.
  • Post-production ensures the finalization of all production GMP documentation.
  • Plans and coordinates global production for all projects in GMP.
  • Generate documentation to support product files and reports for clients.
  • Could occasionally be in direct contact with clients.
  •  Ensures housekeeping of production areas.
  •  Centralizes Time Sheet for Production Experts and manages leave or absence request.
  •  In collaboration with other supervisors/managers of production ensures appropriate resource allocations to the various projects of Production Department.
  •  Ensures his/her team is adequately staffed, trained, equipped (premises, equipment and any material) to execute required work.
  • This covering both GMP and EHS aspects.
  •  Participated to the lab activity with the technicians.

Candidate profile

  • At least 3 years experience in cGMP and manufacturing environment.
  • Experience in people management.
  • Organization skills, multitasking.
  •  Quality minded, autonomous, rigorous, attentive to details, persevering and proactive.
  • Teamwork and teaching skills.
  • Good communication skills and cheerful.
  • Strong communication skills and fluent in English and French.

Offer

  • Full-time position (40h/week).
  • An indeterminate contract.
  • The opportunity to take part in a growing dynamic biotech company.
  • A human-sized working environment with a convivial atmosphere.
  • A company car with fuel card.

Contact Details

Interested? Send your resume and a cover letter at job@masthercell.com