Amneal Pharmaceuticals logo

Transdermal Operator I - 12 Hour Schedule -Day Shift

Job Overview

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Employment Type

Full-time
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Compensation

Hourly
Range $18.50 - $26.00
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Work Schedule

Rotating Shifts
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Benefits

Health Insurance
Dental Insurance
Paid Time Off
401(k) matching
Performance bonus
Employee wellness programs
safe work environment

Job Description

Amneal Pharmaceuticals is a renowned pharmaceutical company dedicated to delivering high-quality medications and healthcare solutions worldwide. As a key player in the pharmaceutical manufacturing sector, Amneal operates under rigorous cGMP (current Good Manufacturing Practice) regulations to ensure the highest standards of product safety and efficacy. The company is committed to innovation, operational excellence, and compliance, upholding a strong ethical framework in its manufacturing processes. Amneal not only emphasizes quality but also prioritizes employee development and a supportive work environment, fostering a culture of teamwork, respect, and continual improvement.

The role of Transdermal Operator I at Amneal is essential within the transdermal manufacturing and packaging team. This position involves supporting production in a cGMP-regulated environment, with duties that include operating manufacturing and packaging equipment under supervision, assisting with mixing, coating, and converting activities, and performing critical in-process inspections to maintain product quality. The role requires meticulous attention to detail, the ability to accurately document batch activities, and a strong commitment to health and safety standards. Employees in this role work rotating day shifts of 12 hours each, from 6:00 AM to 6:30 PM, which demands a flexible and dedicated approach to work schedules.

Transdermal Operator I is an entry-level position suited for candidates with at least one year of experience in a manufacturing or GMP-regulated environment. The role is designed for individuals who are eager to learn and develop their skills in pharmaceutical manufacturing processes. Employees will engage in equipment setup, qualify manufacturing batches according to protocols such as IQ/OQ/PQ and ANDA, and participate in commercial batch activities that support production goals. The position requires performing packaging room clearance, conducting material reconciliation, and ensuring the manufacturing area and equipment are cleaned and maintained appropriately after each batch.

Working at Amneal offers personnel the opportunity to contribute towards producing life-enhancing medications while adhering to strict regulatory and safety standards. The position offers an hourly wage ranging from $18.50 to $26.00, reflecting aptitude and experience. In addition to the hourly wage, there is a short-term incentive plan available, which may include bonuses or performance-based awards granted within the first year of employment. This makes the role not only rewarding professionally but also financially. Amneal promotes a balanced work-life culture supported by comprehensive benefits and ample growth prospects in the pharmaceutical manufacturing field.

Job Requirements

  • High School or GED
  • One 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 lift up to 40 lbs
  • Flexibility to work extended hours when required

Job Qualifications

  • High School or GED
  • One 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
  • Ability to 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


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