Validation Engineer

Barry Wehmiller Design Group

East Brunswick, NJ, United States
Fat, sat, iq, oq documentation
Fda compliance
Pharmaceutical equipment validation
Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment

Job Summary

  • Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.
  • This role will challenge you to be a passionate and successful business family member all while expanding your technical abilities.
  • You will be welcomed into a rapidly growing business and team and empowered to make an impact.

Matching Summary

Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.

Skills & Requirements

Must-have

  • FAT, SAT, IQ, OQ documentation
  • FDA compliance
  • Pharmaceutical equipment validation
  • Automated Systems validation
  • Technical writing
  • Project management support

Nice-to-have

  • Truly Human Leadership culture
  • Entrepreneurial mindset
  • Flexibility with tasks
  • Interacting with all levels of management

Key Requirements

  • Minimum of 3 years project experience with validation
  • Minimum of 3 years project experience in pharmaceutical or medical device environments
  • B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree
  • Willing and able to travel as necessary

Work Rights

Not specified

Tailored Resume

Cover Letter