Transdermal Operator I - 12 Hour Schedule -Day Shift
Amneal Pharmaceuticals
June 26, 2026
On-site
Piscataway, NJ
Operations
The Transdermal Operator I supports transdermal manufacturing and packaging operations in a cGMP-regulated environment. Operate equipment under supervision; assist with basic mixing, coating, and converting activities; perform in-process inspections; complete documentation; and maintain a clean, safe work area.
Day Shift: 12-hour rotating schedule (6:00 AM – 6:30 PM)
Essential Functions:
- Assist with equipment set-up, IQ/OQ/PQ, ANDA, and commercial batch activities per cGMP and SOP requirements.
- Set up and operate packaging, cartoning, and selected transdermal manufacturing equipment under supervision.
- Assist in mixing, coating, and converting by preparing materials, loading equipment, monitoring runs, and making basic adjustments per SOP.
- Perform packaging room clearance, material counts, and reconciliation.
- Conduct in-process checks and visual inspections to ensure product quality.
- Document batch activities, in-process checks, and logbook entries accurately and timely.
- Clean room and equipment after each batch.
- Maintain a clean, organized, and safe work environment; report deviations, equipment issues, or safety concerns to the Supervisor.
- Follow cGMP, SOP, OSHA, and safety requirements; perform other duties as assigned.
Qualifications:
- Education: High School or GED (Required)
- Experience: 1+ year in manufacturing or a GMP-regulated environment
Skills/Abilities:
- English communication; basic math and mechanical aptitude; computer data entry
- Attention to detail; strong documentation practices; teamwork
- Repetitive tasks; lift up to 40 lbs; flexibility for extended hours
Additional Requirement:
- Successful completion of an OSHA-compliant Respirator Fit Test is required.
Compensation: $18.50–$26.00 per hour; short-term incentive opportunity within first 12 months.
Day Shift: 12-hour rotating schedule (6:00 AM – 6:30 PM)
Essential Functions:
- Assist with equipment set-up, IQ/OQ/PQ, ANDA, and commercial batch activities per cGMP and SOP requirements.
- Set up and operate packaging, cartoning, and selected transdermal manufacturing equipment under supervision.
- Assist in mixing, coating, and converting by preparing materials, loading equipment, monitoring runs, and making basic adjustments per SOP.
- Perform packaging room clearance, material counts, and reconciliation.
- Conduct in-process checks and visual inspections to ensure product quality.
- Document batch activities, in-process checks, and logbook entries accurately and timely.
- Clean room and equipment after each batch.
- Maintain a clean, organized, and safe work environment; report deviations, equipment issues, or safety concerns to the Supervisor.
- Follow cGMP, SOP, OSHA, and safety requirements; perform other duties as assigned.
Qualifications:
- Education: High School or GED (Required)
- Experience: 1+ year in manufacturing or a GMP-regulated environment
Skills/Abilities:
- English communication; basic math and mechanical aptitude; computer data entry
- Attention to detail; strong documentation practices; teamwork
- Repetitive tasks; lift up to 40 lbs; flexibility for extended hours
Additional Requirement:
- Successful completion of an OSHA-compliant Respirator Fit Test is required.
Compensation: $18.50–$26.00 per hour; short-term incentive opportunity within first 12 months.