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Technical Service Metrology Supervisor (H/F)

May 11th 2020

MaSTherCell is a dynamic and global Contract Development and Manufacturing Organization (CDMO) on a mission to deliver optimized process industrialization capacities to cell therapy organizations and speed up the arrival of their therapies to the market. From technology selection to business modelling, through GMP manufacturing, process development, quality services, MaSTherCell’s teams are fully committed to helping their clients fulfil their objective of providing sustainable and affordable therapies to their patients.

Mission Description

The Metrology Supervisor is responsible of all equipment aspects in the facility.

He/she supervises the management of all new equipment and their commissioning in the facility, including :

  • Uniformity of User Requirement Specifications, Equipment ordering and Qualification;
  • Follow-up of the sub-contractors and their planning of intervention and Production, QC and Supply Chain activities;
  • Management of a centralized database in an up-to-date state;
  • Management of the pool of equipment within the facility in terms of preventive and curative maintenance;
  • Follow-up of DEV/CAPA and CHC ; ensuring opening in due time, efficient actions proposals and closure in due time;
  • Centralized EMS (Environmental Monitoring System) system management and alarms follow-up.

He/she ensures adequate GMP level through his function and contributes to continuous improvement in his department and in the plant.

He/she leads maintenance and requalification’s activities, in accordance with initial agreed planning’s and the action log related to troubleshooting/repair actions is leading and respects the timelines.

He/she is the interface between the Technical Service department and all other MaSTherCell’s departments and customer for technical aspects related to the equipment management.

He/she Takes part to audits when necessary ; He/She is involved in preparation and execution of any audits/inspection.

He/she Drafts/reviews Masthercell documents related to his/her activities (protocols, reports, procedures, forms, instructions, …) and reviews documentation (protocols or reports) filled in by other;

Candidate profile

OBLIGATORY REQUIREMENTS

  • Engineer in Science (e.g : in biology, pharmacy, clinical chemistry, bioengineering) or relevant expérience in a similar position in the sector of Biotech/Pharma/Cell Therapy.
  • At least 5 years of experience in GMP environment.
  • Aseptic production is a plus.
  • Fluency in French.
  • Good reading comprehension and writing skills in English.

USEFUL REQUIREMENTS

  • Technical oriented
  • Quality minded, rigorous, customer oriented and continuous improvement driven
  • Demonstrated cross functional team spirit.
  • Organisation Skills, multitasking, flexibility and autonomous.
  • Good communicator.
  • Computer skills : Microsoft Office, use of Data Base systems

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

To apply for this job, please send your application on the following link : https://bit.ly/2yL0pBU