ABOUT COMPLIANCE TEAM
Since 2003, our life science compliance consultants have helped pharmaceutical and medical device manufacturers bring lifesaving products to market. We provide engineering validation services and FDA regulatory affairs services to life science companies across the United States. We are seeking a creative, collaborative, and hands-on worker to provide quality support in a large manufacturing environment. We value personal accountability, corporate transparency, and professional development – a positive customer experience is as important as a positive employee experience. We thrive on hard work and fun!
Position Description
Compliance Team is sourcing for an experienced Manufacturing Process Engineer to support a 3 - 4 month project in Buffalo, NY.
Requirements include:
Expert knowledge of 21CFR820, cGMP and cGDP
10+ years experience in validation of Medical Device Manufacturing Equipment
Activities include:
- Creation of process SOPs and Work Instructions
- Development of IOPQ protocols
- Execution of IOPQ protocols
Job Types: Contract, Temporary
Pay: $70.00 - $80.00 per hour
Expected hours: 40 per week
Benefits:
- Flexible schedule
Schedule:
- 8 hour shift
- Monday to Friday
Work Location: Hybrid remote in Raleigh, NC 27601