Support GMP compliance, facility operations, and development activities in a fast-growing
peptides and biologics startup.
• Support GMP compliance for development labs, pilot plant, and clean areas
• Perform daily GMP walkthroughs and housekeeping checks
• Support environmental monitoring review and area clearance
• Assist in equipment qualification documentation (IQ/OQ/PQ)
• Prepare, review, and control SOPs, development batch records, and protocols
• Maintain document control and ensure GDP compliance
• Initiate and track deviations, change controls, and CAPAs
• Support vendor qualification, material release, and training coordination
• Assist in internal and client audits and scale-up activities
Excellent knowledge of GMP, GLP, and documentation practices
Understanding of peptides/biologics (or strong learning attitude)
Good communication and documentation skills