April 24th 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. To lead its increasing number of development and manufacturing projects, MaSTherCell is looking for a highly motivated Production Supervisor.

Mission Description

Manage and enforce established GMP production process; ensure safety standards are in compliance;

  • Plan and coordinate global production for all projects in GMP ; Maintain time and attendance of all production employees and ensure staffing is adequate and within established guidelines with the project - regular contact with the client;
  • Review production procedures and system reports to ensure all data input and record and report are accurate; generate documentation to support product file and reports for client; Post-production, ensure the finalization of all production GMP documentation;
  • Team Management: develop and drives team objectives, direction & priorities - communicate performance standards to the team, recognizing and rewarding team accomplishments and counseling performance problems ;
  • Promote and ensure productive communication between team members and management;
  • Ensure all employees are properly trained and equipped in current process to execute required work;
  • Participate in customer and authority audits;
  • Drive continuous improvement initiatives and implementation of Operational Excellence.

Candidate profile


  • Master degree in life sciences, biology, pharmacy, clinical chemistry, bioengineering or relevant experience in a similar position in the sector of Biotech/Pharma/Cell therapy;
  • At least 5 years experience in cGMP and manufacturing environment;
  • Must have excellent team ad time management;


  • Effective communication skills;
  • Quality minded, rigorous, customer oriented and continuous improvement drive;
  • Problem solving as well as written and verbal communication skills;
  • Organization skills, multitasking, flexibility and autonomy;


  • 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.

Contact Details

To apply for this job, please send your application on the following link : MasTherCell