Transdermal Operator I - 12 Hour Schedule -Day Shift
Amneal Pharmaceuticals
5 months ago
On-site
Piscataway, NJ
Operations
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 performing basic adjustments per SOP.
- Perform packaging room clearance, material counts, and reconciliation activities.
- Conduct in-process checks and visual inspections to ensure product quality.
- Document batch activities, in-process checks, and logbook entries accurately and timely.
- Perform room and equipment cleaning after each batch.
- Maintain a clean, organized, and safe work environment.
- Report deviations, equipment issues, or safety concerns to the Supervisor.
- Follow all cGMP, SOP, OSHA, and safety requirements.
- Perform other duties as assigned.
Qualifications:
- Education: High School or GED (Required)
- Experience: 1+ year in Manufacturing or GMP-regulated environment
- Skills/Abilities: English communication; basic math and mechanical aptitude; computer systems/data entry; attention to detail and documentation; teamwork; repetitive tasks and lifting up to 40 lbs; flexibility for extended hours.
- Additional Requirement: OSHA-compliant Respirator Fit Test completion (required).
Compensation/Benefits (as stated): Hourly rate $18.50–$26.00; short-term incentive/bonus opportunity within first 12 months; comprehensive benefits program including health/insurance and 401(k) matching for eligible positions.
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 performing basic adjustments per SOP.
- Perform packaging room clearance, material counts, and reconciliation activities.
- Conduct in-process checks and visual inspections to ensure product quality.
- Document batch activities, in-process checks, and logbook entries accurately and timely.
- Perform room and equipment cleaning after each batch.
- Maintain a clean, organized, and safe work environment.
- Report deviations, equipment issues, or safety concerns to the Supervisor.
- Follow all cGMP, SOP, OSHA, and safety requirements.
- Perform other duties as assigned.
Qualifications:
- Education: High School or GED (Required)
- Experience: 1+ year in Manufacturing or GMP-regulated environment
- Skills/Abilities: English communication; basic math and mechanical aptitude; computer systems/data entry; attention to detail and documentation; teamwork; repetitive tasks and lifting up to 40 lbs; flexibility for extended hours.
- Additional Requirement: OSHA-compliant Respirator Fit Test completion (required).
Compensation/Benefits (as stated): Hourly rate $18.50–$26.00; short-term incentive/bonus opportunity within first 12 months; comprehensive benefits program including health/insurance and 401(k) matching for eligible positions.