Associate Process Engineer

GForce Life Sciences

Mahwah, NJ0–2 yrs3h agovia LinkedIn

12-month Contract

Onsite in Mahwah, NJ

Must be able to work on a W2

What You’ll Do

  • Support development and modification of process formulations, methods, and controls to meet quality standards.
  • Recommend and help implement process/documentation improvements and updates.
  • Review product development requirements for compatibility with processing methods to help determine costs and schedules.
  • Integrate equipment and material capabilities to meet process module and technology target specifications.
  • Draft, execute, and close IQ/OQ/PQ protocols for production lines and equipment.
  • Collect, compile, and analyze experimental/process data using statistical methods; write clear validation final reports.
  • Support change control efforts by evaluating engineering change orders (ECOs) and process modifications for validation impact and re-validation needs.
  • Draft and update SOPs, work instructions, preventative maintenance procedures, and equipment operating manuals based on validated parameters.

Must-Have Qualifications

  • Mechanical Engineering or similar background.
  • Proficient technical writing skills (SOPs and validation documentation).
  • Ability to work under pressure and collaborate with other engineers to deliver documentation updates.

Nice-to-Have

  • Hands-on, mechanically inclined approach.
  • OnePLM/Windchill experience.
  • Validation experience.
  • Design review experience.

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