Manufacturing Technician - Labeling 2nd shift

Stokes Pharmacy•Mount Laurel Township, NJ

7d•Onsite

About The Position

The Manufacturing Technician – Labeling works in a cGMP environment alongside other labeling technicians and 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 position operates primarily in a controlled laboratory environment and involves using standard office equipment, frequent standing and walking, and compliance with company gowning and operational requirements. The schedule is Monday through Thursday, 10:00 a.m. to 8:00 p.m.; schedules may vary at times. Starting pay is $20 per hour, plus a shift differential and twice-yearly bonuses.

Requirements

High school diploma or GED.
Exceptional attention to detail.
Ability to work in a fast-paced environment with little assistance from the Supervisor.
Capability to work with small, delicate pieces of 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 skills, including the ability to interpret operating and maintenance instructions and procedure manuals.
Basic arithmetic skills, including addition, subtraction, multiplication, and division with decimals and fractions when checking reports, forms, records, and comparable data.
Ability to solve practical problems and handle concrete variables in standardized situations, and interpret written, oral, diagram, or schedule-based instructions.
Ability to lift up to 25 pounds on occasion, stand and walk for most of the shift, and sit and/or stand for 8–10 hours or more per day as needed.

Nice To Haves

Labeling or quality assurance experience; preferred but not required.
cGMP experience; preferred but not required.
Knowledge of 21 CFR Part 210 and 211 for cGMP operations must be developed.

Responsibilities

Practice current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDocP).
Coordinate with QA 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 equipment maintenance logbooks for designated equipment.
Keep concurrent records, including charts, logbooks, and other pertinent documentation.
Complete support documentation for operations in accordance with GDocP.
Manage time effectively during batch processes, including shift changes during batch preparation.
Report unusual or non-routine occurrences when performing tasks using an NOE report.
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 used to record or trace tasks performed.
Follow company gowning and operational requirements.
Clean and maintain environmentally controlled areas.
Collaborate with manufacturing team members and other departments, including quality and facility maintenance, to achieve company goals.
Coordinate with Supply Chain Technicians to maintain in-stock labeling and packaging materials.
Practice safe work habits and maintain a safe work environment.