cGMP Associate III (A Team)

We are seeking a cGMP Associate III to serve as an area expert in manufacturing, providing technical leadership, troubleshooting, and guidance to less experienced associates. This role requires a strong focus on safety, quality, and output, with a goal of consistently meeting production goals while maintaining compliance with all GMP, GDP, FDA, ISO 13485, and safety requirements.

Requirements

• High school diploma or equivalent
• 2–4 years of experience in a GMP-regulated manufacturing environment
• Fully qualified and trained on all equipment within the manufacturing area
• Strong understanding of GMP, GDP, FDA, and ISO 13485 compliance standards
• Demonstrated ability to troubleshoot and resolve complex equipment and process issues
• Proven track record of mentoring, coaching, or providing guidance to peers
• Excellent attention to detail, problem-solving, and communication skills
• Comfortable working in a fast-paced, team-driven environment

Benefits

• 401(k) with up to a 6% employer match
• Employee stock purchase plan
• Flexible time off
• Vacation accrual (three to five weeks annually)
• Paid sick time (up to 64 hours annually)
• Paid and/or floating holidays
• Parental leave
• Short- and long-term disability insurance
• Tuition reimbursement
• Health and welfare benefits