Supervisor, Transdermal
Amneal Pharmaceuticals
9 hours ago
On-site
Piscataway, NJ
Operations
Responsibilities:
- Oversee manufacturing floor operations; ensure safety, quality, and productivity with 100% GMP compliance.
- Plan and schedule manufacturing and packaging activities to meet deadlines and prevent backorders.
- Partner with the quality group to ensure compliance; participate in departmental investigations.
- Support R&D and execution of new products; provide key input.
- Serve as a Working Supervisor: manufacture R&D batches (large/small scale), train operators on processing and equipment capabilities.
- Participate in equipment setup, IQ/OQ/PQ, and commercial batch activities; set up, run, and clean equipment in a GMP environment; perform mixing, coating, converting, pouching, and cartoning.
- Provide daily communication to staff to keep everyone informed of pertinent departmental/company events.
Additional responsibilities:
- R&D and commercial scale-up activities.
- Perform continuous improvements.
Qualifications:
- Education: BA/BS in a related field (preferred). Associate degree in a related field + 5 years leading and training staff (required).
- Experience: 3+ years in transdermal drug delivery or manufacturing GMP environment; 3+ years leading and training staff.
- Specialized knowledge: Transdermal, converting, and packaging experience in a GMP manufacturing environment.
Additional requirement:
- Successful completion of an OSHA-compliant respirator fit test.
Compensation/Benefits (as stated):
- Base salary: $80,000–$100,000 per year; eligible positions include health/insurance benefits and a 401(k) matching contribution.
- Oversee manufacturing floor operations; ensure safety, quality, and productivity with 100% GMP compliance.
- Plan and schedule manufacturing and packaging activities to meet deadlines and prevent backorders.
- Partner with the quality group to ensure compliance; participate in departmental investigations.
- Support R&D and execution of new products; provide key input.
- Serve as a Working Supervisor: manufacture R&D batches (large/small scale), train operators on processing and equipment capabilities.
- Participate in equipment setup, IQ/OQ/PQ, and commercial batch activities; set up, run, and clean equipment in a GMP environment; perform mixing, coating, converting, pouching, and cartoning.
- Provide daily communication to staff to keep everyone informed of pertinent departmental/company events.
Additional responsibilities:
- R&D and commercial scale-up activities.
- Perform continuous improvements.
Qualifications:
- Education: BA/BS in a related field (preferred). Associate degree in a related field + 5 years leading and training staff (required).
- Experience: 3+ years in transdermal drug delivery or manufacturing GMP environment; 3+ years leading and training staff.
- Specialized knowledge: Transdermal, converting, and packaging experience in a GMP manufacturing environment.
Additional requirement:
- Successful completion of an OSHA-compliant respirator fit test.
Compensation/Benefits (as stated):
- Base salary: $80,000–$100,000 per year; eligible positions include health/insurance benefits and a 401(k) matching contribution.