Manufacturing Technician - Labeling

Stokes Pharmacy•Mount Laurel Township, NJ

2d•Onsite

About The Position

The Manufacturing Technician works in a cGMP environment with other labeling technicians under the direct supervision of the Manufacturing Manager. The role focuses on meeting individual and team productivity goals while maintaining precision and quality during labeling and packaging operations for sterile and non-sterile products. The technician follows cGMP and Good Documentation Practices, operates and maintains designated equipment, completes batch and support documentation, and coordinates with Quality Assurance, Production, Supply Chain, and other teams. The position is full-time, working four 10-hour days, Monday through Thursday, with a mid-shift schedule of 10:00 a.m. to 8:00 p.m. Work schedules may vary at times. The role operates primarily in a controlled laboratory environment.

Requirements

High school diploma or GED.
Develop knowledge of 21 CFR Part 210 and 211 for cGMP operations.
Exceptional attention to detail.
Ability to work in a fast-paced environment with little assistance from the Supervisor.
Ability to work with small, delicate machinery and labels.
Strong organizational skills.
Basic computer skills.
Ability to work independently and as part of a team.
Punctuality and low absenteeism.
Fluent English reading, writing, speaking, and comprehension, including the ability to interpret operating and maintenance instructions and procedure manuals.
Basic mathematical skills, including calculations with decimals and fractions when checking reports, forms, records, and comparable data.
Ability to solve practical problems in substantially standardized situations and interpret written, oral, diagram, or schedule-based instructions.

Nice To Haves

Labeling or quality assurance experience.
cGMP experience.

Responsibilities

Follow current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDocP) at all times.
Coordinate with Quality Assurance for Master Batch Label approval and with Production for Production Batch Label approval.
Label, cap, package, and inspect in-process and final sterile and non-sterile products.
Set up and operate equipment used in labeling and packaging processes.
Maintain maintenance logbooks for designated equipment.
Complete concurrent records, including charts, logbooks, and other pertinent documentation.
Complete support documentation for labeling, inspection, and other operations in accordance with GDocP.
Manage time effectively during batch processes, including shift changes during batch preparation.
Report unusual or non-routine occurrences through NOE reports.
Keep training up to date and assist in training technicians.
Attend training classes, workshops, and meetings as required to improve job skills and product-related procedures.
Contribute to the development of standard operating procedures, batch records, equipment logs, and other documentation related to task history or traceability.
Follow company gowning and operational requirements.
Clean and maintain environmentally controlled areas.
Collaborate with manufacturing team members and departments such as Quality and Facility Maintenance to achieve company goals.
Coordinate with Supply Chain Technicians to maintain in-stock labeling and packaging materials.
Use safe work habits and help maintain a safe work environment.