Process Specialist - MSAT

Process Specialist - MSAT

Lonza

Geleen, Netherlands

As a Process Specialist within MSAT, you support manufacturing operations as a process and product Subject Matter Expert. In this hands-on role, you work closely with production teams and clients on-site to ensure smooth execution of manufacturing runs, provide technical support during deviations and contribute to continuous process improvement in a dynamic Cell & Gene Therapy environment. This role offers a strong next step for professionals looking to grow from operational or laboratory roles into MSAT and process support.

What you will get

  • A key role at the interface of MSAT and Manufacturing in a GMP environment;
  • The opportunity to work on innovative Cell & Gene Therapy processes;
  • Close collaboration with cross-functional teams including Manufacturing, QA, QC and Engineering;
  • Exposure to real-time decision making and client interactions during production runs;
  • Opportunities to grow into a process SME within Lonza;
  • A clear pathway to develop into more advanced MSAT or process expert roles;
  • Compensation programs that recognize high performance;
  • A variety of benefits dependent on role and location.

What you will do

  • Support and monitor manufacturing runs on-site together with the client (PIP);
  • Provide technical input during deviations and real-time issue resolution during ongoing runs;
  • Participate in DRBs and act as the MSAT contact for process-related topics;
  • Perform or support investigations related to process deviations;
  • Support data collection and analysis for process capability and trend evaluations;
  • Lead or support change controls (CRs) and process improvements;
  • Ensure clear handovers between teams and maintain alignment with MSAT and manufacturing.

What we are looking for

  • Bachelor’s degree in Biotechnology, Life Sciences or a related discipline;
  • Experience in a Cell & Gene Therapy, biopharma or GMP manufacturing environment is preferred;
  • Knowledge of GMP, ATMP or aseptic manufacturing processes is a plus;
  • Experience with deviation and change management systems (e.g. TrackWise) is beneficial;
  • Ability to work independently and make decisions in a fast-paced production environment;
  • Strong communication skills and ability to collaborate across teams and with clients;
  • Flexibility in working hours, with willingness to support operations outside standard hours and adapt to future operational needs.

Don't forget to mention EuroPharmaJobs when applying.

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