What are the responsibilities and job description for the Manufacturing Deviation Investigator position at i-Pharm GxP?
Manufacturing Deviation Investigator – Remote with Occasional Travel
A world-class biopharmaceutical manufacturing site is expanding, driving large-scale production of advanced therapies. To support this growth, an experienced Manufacturing Deviation Investigator is needed to ensure compliance, conduct root cause analyses, and improve processes.
This role is primarily remote, with occasional travel to Lebanon, IN, to support critical investigations.
Key Responsibilities:
- Investigate manufacturing deviations, identifying root causes and implementing corrective actions.
- Ensure compliance with FDA, GMP, and site-specific quality standards.
- Collaborate with cross-functional teams to drive continuous improvement.
- Prepare and document high-quality deviation reports.
Ideal Candidate:
- Strong experience in deviation investigations within pharmaceutical or biologics manufacturing.
- In-depth knowledge of GMP regulations and root cause analysis techniques.
- Excellent technical writing and problem-solving skills.
Contract Details:
- Duration: 12-month contract, extension based on performance.
- Work Setup: Remote with occasional site travel.
- Engagement: W2 only.
- Rate: Competitive, based on experience.
Join a high-impact team at the forefront of pharmaceutical innovation. Apply today!
Hamish Corson
Senior Business Manager | USA | GxP Contract Division
1 646 536 4736 (USA)
HCorson@i-pharmconsulting.com