Validation Engineer Ii, Production Equipment & Utilities Gmp
Thermo Fisher Scientific UK
Tilburg, Netherlands
Commissioning and qualification experience
Gmp regulated environment expertise
C&q iq oq pq protocol implementation
This role ensures flawless execution of equipment, utilities, facilities qualification, and process validation activities within a highly regulated pharmaceutical setting
Job Summary
This role ensures flawless execution of equipment, utilities, facilities qualification, and process validation activities within a highly regulated pharmaceutical setting.
The successful candidate will work closely with technical, development, quality, and production teams to meet world-class validation standards.
Candidates must demonstrate proven hands-on experience in Commissioning & Qualification and Validation gained in a pharmaceutical environment.
Matching Summary
This role ensures flawless execution of equipment, utilities, facilities qualification, and process validation activities within a highly regulated pharmaceutical setting.
Skills & Requirements
Must-have
Commissioning and Qualification experience
GMP regulated environment expertise
C&Q IQ OQ PQ protocol implementation
Utilities validation HVAC water air
User Requirement Specifications drafting
Nice-to-have
Integrity intensity innovation involvement traits
Matrix organization leadership experience
Internal and external audit support
Periodic review report generation skills
Key Requirements
Bachelor's degree or equivalent experience required
Prior validation and GMP manufacturing experience mandatory
Technology science or related field background preferred