Engineer Ii, Computer Systems Validation

Thermo Fisher Scientific UK

Greenville, NC, US
Onsite
Bachelor's degree in engineering or life sciences
Knowledge of cgmp and regulated environments
Experience with iq/oq/pq validation protocols
This role supports validation activities tied to automation systems and manufacturing equipment across the site

Job Summary

  • This role supports validation activities tied to automation systems and manufacturing equipment across the site.
  • You will partner closely with automation, manufacturing, and quality teams to ensure regulatory compliance and product quality.
  • The position offers a collaborative team environment within a global leader providing integrated drug development solutions.

Matching Summary

This role supports validation activities tied to automation systems and manufacturing equipment across the site.

Skills & Requirements

Must-have

  • Bachelor's degree in Engineering or Life Sciences
  • Knowledge of cGMP and regulated environments
  • Experience with IQ/OQ/PQ validation protocols
  • Familiarity with PLC, SCADA, DCS, DeltaV systems
  • Strong technical writing and documentation skills

Nice-to-have

  • 2 years experience in CSV or GMP environment
  • Collaborative team player with strong communication
  • Detail-oriented and adaptable to fast-paced work
  • Exposure to change management processes
  • Ability to manage multiple tasks effectively

Key Requirements

  • Bachelor's degree in Engineering, Life Sciences, Chemistry, or related field
  • Equivalent combinations of education, training, and relevant experience may be considered
  • Not specified

Work Rights

Not specified

Tailored Resume

Cover Letter