Drug Manufacturing Technician-2nd Shift

Job Title: Drug Manufacturing Technician
Location: Gretna, Louisiana
Shift: 2 ^nd Shift Monday–Friday | 5:00 PM – 10:30 PM
Status: Non-Exempt (Overtime paid at 1.5x for hours worked over 40)
Position Summary
The Drug Manufacturing Technician is responsible for supporting pharmaceutical manufacturing operations through the safe, accurate operation and maintenance of production equipment. This role involves weighing and blending raw materials and active ingredients, maintaining detailed batch records, and ensuring compliance with cGMP, safety, and quality standards. This is an entry-level manufacturing role with structured procedures and training provided. Key Responsibilities

• Operate and maintain drug manufacturing equipment in accordance with established procedures and safety guidelines.
• Accurately weigh raw materials and active pharmaceutical ingredients (APIs) and combine them into blends per batch instructions.
• Complete batch records, logbooks, and manufacturing documentation in compliance with cGMP requirements.
• Ensure all documentation is completed accurately with minimal errors or corrections.
• Perform routine cleaning and housekeeping of equipment and manufacturing areas to maintain a state of good repair and readiness.
• Participate in work orders, production activities, and equipment setup or changeover as required.
• Follow all written procedures exactly, including manufacturing instructions, safety protocols, and quality standards.
• Complete all required training, including cGMP, safety, and job-specific training, within assigned timelines.
• Work independently or collaboratively as part of a manufacturing team to meet production goals.

Required Qualifications

• High School Diploma or GED required.
• Ability to read, understand, and strictly follow written procedures and instructions.
• Strong attention to detail and commitment to accuracy and documentation compliance.
• Ability to work independently with minimal supervision as well as in a team environment.
• Willingness to work in a regulated pharmaceutical manufacturing environment.

Preferred Qualifications

• Previous experience in pharmaceutical, chemical, food, or regulated manufacturing environments.
• Familiarity with cGMP principles and batch record documentation.
• Basic mechanical aptitude or experience working with manufacturing equipment.

Work Environment & Physical Requirements

• On-site manufacturing role in a controlled production environment.
• Standing, walking, lifting, and handling of materials as part of routine duties.
• Compliance with PPE, safety, and contamination control requirements is mandatory.

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.