Transdermal Operator I - 12 Hour Schedule -Day Shift

Amneal

1d•Onsite

About The Position

The Transdermal Operator I supports transdermal manufacturing and packaging operations in a cGMP-regulated environment. This role includes operating equipment under supervision, assisting in basic mixing, coating, and converting activities, performing in-process inspections, completing documentation, and maintaining a clean and safe work area.

Requirements

High School or GED - Required
1 year or more 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.
Successful completion of an OSHA-compliant Respirator Fit Test is required.

Responsibilities

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.