The Senior Equipment & System Specialist will manage the lifecycle of equipment across point-of-care facilities in the US, ensuring compliance and efficient functionality. Initial onboarding and training will be conducted in Belgium (client-funded travel).

 

• Deploy new instruments within Point of Care Manufacturing network

• Coordinate and oversee instrument qualification and maintenance

• Ensure data integrity and user management compliance

• Review vendor documentation (IOQ, PQ) and write lifecycle documents (URS, IQ, OQ, PQ)

• Conduct root-cause analysis and implement corrective actions for deviations

 

• BSc/MSc in Life Sciences, Biotechnology, Engineering, or related field with 5-10 years of experience

• Knowledge of cGMP equipment lifecycle requirements, GMP, ICH guidelines, and ATMP regulations

• Experience with computer system validations (preferred)

• Strong communication skills; fluent in English

• US-based, willing to travel up to 50% (key locations: Boston, San Francisco, San Diego)

 

• Quality-driven, adaptable to changing priorities, and fosters continuous improvement