Terumo Blood and Cell Technologies
Sterilisation Engineer

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STERILIZATION ANALYST / ENGINEER
(Ref No:26_29)
Terumo BCT Ltd, based in Larne, manufactures a range of sterile fluids for both human and veterinary use. We currently have an exciting opportunity for a CQV Sterilisation Analyst/Engineer to join our team. The successful candidate will be responsible for supporting and performing validation activities associated with terminal sterilisation processes.
We are seeking motivated individuals to join our Sterilisation Validation Department. There are currently two opportunities available: one permanent full-time position and one fixed-term maternity cover position. Comprehensive training will be provided to ensure the successful candidate is fully supported in developing the knowledge and skills required for the role.
Duties
- Autoclave sterilisation cycle development, validation and annual re-qualification of cycles.
- Process qualification including all areas of the validation life cycle.
- Operation of steam and superheated water autoclaves.
- Generation and completion of validation documentation (protocols and reports) and assist in the execution of qualifications such as IQ/OQ/PQ.
- Recording and analysis of process data including use of statistical process control techniques.
- Investigation, reporting and reviewing of results.
- Calibration of process equipment and measurement instrumentation.
- Working with cross function departments on all aspects of the sterilisation process.
- To ensure that good GMP/QMS standards are maintained at all times.
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Requirements
Applicants must possess:
- A degree or equivalent qualification in Microbiology/Biology Science or Engineering, e.g. Chemical or Biomedical Engineering or relevant experience in quality, validation or manufacturing.
- Strong communication and writing skills.
- Good time management and planning skills.
- Ability to work under pressure and to strict deadlines – (this role may necessitate working additional hours and/or shifts, including weekend shifts as and when required.


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In addition, the following would be a distinct advantage:
- Experience within a Pharmaceutical or Medical Device environment.
- Knowledge of moist heat sterilisation and regulations.
- A track record of carrying out and executing GMP documentation.
- Experience gained within a production/manufacturing environment.
If you're ready to make a significant impact in a dynamic and collaborative environment, we invite you to apply for this exciting opportunity. Please submit your CV via our Terumo BCT career’s portal mySource before the closing date of 5:00 pm on Thursday, 01 October 2026.
You must clearly demonstrate on your CV / application how you meet the required criteria as failure to do so may result in you not being shortlisted.
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