Transdermal Manufacturing Technician II — 12-Hour Shift

Amneal Pharmaceuticals; Piscataway Township (NJ); On-site; USD 61,992,000 - 82,656,000; Full time

Benefits offered by this job

Health insurance

401(k) matching

Employee well-being programs

Job summary

Amneal Pharmaceuticals in Piscataway, NJ is hiring a Transdermal Operator II to support advanced pharmaceutical manufacturing in a cGMP environment. This role suits individuals with mechanical or manufacturing backgrounds who want hands-on experience with complex equipment.

The day shift runs 12 hours from 6:00 AM to 6:30 PM with alternating weekends. Responsibilities include setting up and running automated equipment, performing in-process checks, and documenting GMP activities.

Qualifications

• High School Diploma or GED required.
• Mechanical/electrical/manufacturing degrees encouraged to apply.
• OR 3+ years in manufacturing, trades, construction, machining, or other technical roles.
• Strong mechanical aptitude, troubleshooting ability, and attention to detail.
• Good math skills and comfort with precision work.

Responsibilities

• Set up, operate, and troubleshoot automated manufacturing equipment
• Execute R&D, scale-up, ANDA, and commercial batch activities
• Conduct in-process checks, visual inspections, and accurate GMP documentation
• Complete material reconciliation, room clearance, and batch closeout
• Maintain a clean, safe, and compliant work area

Skills

Mechanical aptitude

Attention to detail

Troubleshooting

Math skills

Education

High School Diploma or GED

Mechanical / Electrical / Manufacturing degree

Job description

Amneal Pharmaceuticals in Piscataway, NJ is hiring a Transdermal Operator II to support advanced pharmaceutical manufacturing in a cGMP environment. This role suits individuals with mechanical or manufacturing backgrounds who want hands-on experience with complex equipment.

The day shift runs 12 hours from 6:00 AM to 6:30 PM with alternating weekends. Responsibilities include setting up and running automated equipment, performing in-process checks, and documenting GMP activities.