Gmp Technician

Join a cutting-edge pharmaceutical manufacturing facility specializing in the production of liquid pharmaceutical products. This role offers the opportunity to gain valuable experience in Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs) within a state-of-the-art environment.

Responsibilities

• Follow SOPs, GMPs, and all FDA regulations to ensure compliance.
• Conduct component preparation, aseptic cleaning, and equipment processing.
• Set up and inspect filling lines, maintaining and troubleshooting equipment as needed.
• Perform quality checks and document information accurately.
• Gown up for the majority of the shift and work within clean rooms.
• Stock, gather, and stage manufacturing supplies and equipment.
• Gather, stage, and return production materials as required to support GMP manufacturing activities.

• High School Diploma or GED.
• Experience in GMP, FDA, or strict SOP environments.
• Comfortable with aseptic gowning for the majority of the shift.
• Ability to perform repetitive tasks and excellent attendance.

• Prior Quality Control experience is a plus.
• Candidates must not be colorblind due to inspection area requirements.

This role operates in a pharmaceutical manufacturing facility with a shift schedule of Monday to Friday, 10 PM to 6:30 AM, with occasional overtime of 1-2 hours a day. Training on the first shift for up to 1-2 months is required. The environment is FDA regulated, requiring adherence to a no-talking policy in manufacturing areas. Candidates must stand throughout the shift and cannot wear makeup, nail polish, acrylic nails, or perfume/fragrance in compliance with FDA regulations.

Pay and Benefits

The pay range for this position is $21.25 - $21.25/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Hilliard,OH.

Application Deadline

This position is anticipated to close on Aug 15, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email ... for other accommodation options.