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Job ID :
44145BR
Location :
US - California - San Jose
:
Job Description

When you’re part of the team at Thermo Fisher, you’ll do important work. And you’ll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of $17 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

Position Summary:

Plan, lead, and execute process and software validation project assignments including evaluation, development and monitoring of manufacturing validated systems.

Key Responsibilities:

  • Writes and executes process validation/verification protocols (IQ OQ PQ) for development/manufacturing test, equipment, systems and processes including re-assessment/re-validation activities.
  • Writes and executes software validation plans, requirements, protocols, SOPs and reports.
  • Provide guidance/preparation of process documents (Operating Procedures and/or Work Instructions and forms/templates).
  • Interface with the appropriate Technical and QA personnel to obtain and understand current and new process activities.

Desired Requirements/Qualifications:

  • Upper division bachelor’s student in Engineering or Life Sciences required.
  • Must be team oriented and have excellent interpersonal skills.
  • Must have excellent written and verbal communication skills with ability to clearly articulate requirements and approach to business process owners.
At Thermo Fisher Scientific, each one of our 50,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.



Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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