
Job Overview
Employment Type
Hourly
Compensation
Hourly
Range $18.50 - $26.00
Work Schedule
Night Shifts
Benefits
Health Insurance
Dental Insurance
Paid Time Off
401(k) matching
Performance bonus
Employee wellness programs
inclusive work environment
Job Description
Amneal Pharmaceuticals is a global, integrated specialty pharmaceutical company committed to developing, manufacturing, and delivering high-quality medicines that make a difference in patients' lives. As a prominent player in the pharmaceutical manufacturing industry, Amneal focuses on innovative formulations and complex dosage forms with a deep dedication to compliance with current Good Manufacturing Practices (cGMP) and regulatory standards. The company prides itself on fostering an inclusive, diverse, and dynamic workforce where employees are valued and supported. Amneal is recognized for its comprehensive benefits and continuous opportunities for professional growth within a collaborative environment.
This position is for a Transdermal Operator I within Amneal, specifically supporting transdermal manufacturing and packaging operations in a cGMP-regulated environment. The role operates on a night shift with a 12-hour rotating schedule from 6:00 PM to 6:30 AM. The primary responsibility of this role is to operate equipment under supervision while assisting in mixing, coating, and converting activities related to transdermal products. The operator will be engaged in in-process inspections, material preparation, equipment setup, and maintaining thorough and accurate documentation practices. Emphasis is placed on adhering to cGMP, SOPs, OSHA, and safety requirements to ensure high product quality and workplace safety.
The Transdermal Operator I will assist with equipment set-up, support IQ/OQ/PQ qualification processes, and participate in batch manufacturing activities. Key duties include setting up packaging and manufacturing equipment, performing quality checks, conducting packaging room clearances, and maintaining a clean and organized work area. The role involves detailed record-keeping of batch activities and quick reporting of deviations or equipment malfunctions. Strong attention to detail and teamwork skills are essential for success in this highly regulated environment.
This position requires a High School diploma or GED and at least one year experience in manufacturing or a GMP-regulated setting, demonstrating familiarity with basic manufacturing processes and regulatory standards. The operator should possess basic math and mechanical aptitude, computer proficiency for data entry, and the ability to perform repetitive tasks while lifting up to 40 lbs. Completion of an OSHA-compliant Respirator Fit Test is mandatory. Compensation for this role ranges from $18.50 to $26.00 per hour, with eligibility for short-term incentives such as bonuses or performance-based awards within the first year. The comprehensive benefits package includes diverse health and insurance options, a competitive 401(k) matching program, and employee well-being initiatives designed to support a healthy work-life balance.
This position is for a Transdermal Operator I within Amneal, specifically supporting transdermal manufacturing and packaging operations in a cGMP-regulated environment. The role operates on a night shift with a 12-hour rotating schedule from 6:00 PM to 6:30 AM. The primary responsibility of this role is to operate equipment under supervision while assisting in mixing, coating, and converting activities related to transdermal products. The operator will be engaged in in-process inspections, material preparation, equipment setup, and maintaining thorough and accurate documentation practices. Emphasis is placed on adhering to cGMP, SOPs, OSHA, and safety requirements to ensure high product quality and workplace safety.
The Transdermal Operator I will assist with equipment set-up, support IQ/OQ/PQ qualification processes, and participate in batch manufacturing activities. Key duties include setting up packaging and manufacturing equipment, performing quality checks, conducting packaging room clearances, and maintaining a clean and organized work area. The role involves detailed record-keeping of batch activities and quick reporting of deviations or equipment malfunctions. Strong attention to detail and teamwork skills are essential for success in this highly regulated environment.
This position requires a High School diploma or GED and at least one year experience in manufacturing or a GMP-regulated setting, demonstrating familiarity with basic manufacturing processes and regulatory standards. The operator should possess basic math and mechanical aptitude, computer proficiency for data entry, and the ability to perform repetitive tasks while lifting up to 40 lbs. Completion of an OSHA-compliant Respirator Fit Test is mandatory. Compensation for this role ranges from $18.50 to $26.00 per hour, with eligibility for short-term incentives such as bonuses or performance-based awards within the first year. The comprehensive benefits package includes diverse health and insurance options, a competitive 401(k) matching program, and employee well-being initiatives designed to support a healthy work-life balance.
Job Requirements
- High School diploma or GED
- 1 year or more experience in manufacturing or GMP-regulated environment
- Successful completion of an OSHA-compliant Respirator Fit Test
- Ability to understand and communicate in English
- Basic math and mechanical aptitude
- Ability to use computer systems for data entry
- Ability to perform repetitive tasks and lift up to 40 lbs
- Flexibility to work extended hours when required
Job Qualifications
- High School diploma or GED
- 1 year or more experience in manufacturing or GMP-regulated environment
- Ability to understand and communicate in English
- Basic math and mechanical aptitude
- Ability to use computer systems for data entry
- Strong attention to detail and good documentation practices
- Ability to work as part of a team
- Ability to perform repetitive tasks and lift up to 40 lbs
- Flexibility to work extended hours when required
Job Duties
- 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 operations 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 in a timely manner
- 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
Job Criteria
Experience
No experience required
Job Location
Your Profile Is Visible To Hiring Managers Across OysterLink.
We'll match you with best jobs
Get job offers faster


Search For More Opportunities:
How Candidates Get Hired Faster
Apply to 2–3 similar roles
Complete profile & get best matches
Check new opportunities daily

