Associate Process Engineer
GForce Life Sciences
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.