GMP Manufacturing Technician

GMP Manufacturing Technicians

INTERESTED CANDIDATES PLEASE REACH OUT TO CARRIE AT CSTUDEBA @ACTALENTSERVICES.COM OR TEXT 937. 903. 3402 TO SET UP A PHONE INTERVIEW! The GMP Manufacturing Technicians performs moderately complex to complex manufacturing processes in a highly regulated, climate-controlled environment. This role follows established Standard Operating Procedures (SOPs) to support large-scale pharmaceutical production and offers a strong opportunity for long-term growth in manufacturing. Shifts open: 1st, 2nd and 3rd, rotating 12's and 4 10's Responsibilities

- Perform moderately complex to complex manufacturing processes in accordance with Standard Operating Procedures (SOPs).
- Move totes and materials safely and efficiently to support production activities.
- Prepare and batch large-scale solutions following precise instructions and quality standards.
- Clean manufacturing equipment thoroughly to maintain operational readiness and compliance.
- Steam equipment as required to support sanitation and sterilization processes.
- Prep equipment before use to ensure proper setup, safety, and functionality.
- Follow all regulatory, safety, and quality guidelines within a highly controlled manufacturing environment.
- Maintain accurate and timely documentation of work performed as required by SOPs and regulatory standards.
- Collaborate with team members across rotating shifts to ensure smooth and continuous operations.
- Demonstrate reliability and consistent attendance to support 24/7 manufacturing schedules.

Essential Skills

- High school diploma or GED. Biotech/Pharma Bootcamp programs are great too.
- Reliable work history with strong job tenure.
- Experience in manufacturing, production, or warehousing is preferred.
- Ability to follow detailed Standard Operating Procedures (SOPs) accurately.
- Capability to perform moderately complex to complex processes in a regulated environment.
- Comfort with physical tasks such as moving totes and handling equipment.
- Strong attention to detail and commitment to quality and safety.
- Ability to work a rotating 12-hour night shift schedule.

Additional Skills & Qualifications

- Interest in building a long-term career in pharmaceutical manufacturing.
- Willingness to learn and grow within a large-scale, expanding operation.
- Ability to work effectively in a team-based production environment.
- Strong work ethic and reliability in shift-based roles.

Work Environment This position operates in a highly regulated, climate-controlled pharmaceutical manufacturing environment. Work is performed around large-scale production equipment, solution preparation systems, and sanitation and cleaning processes. The environment emphasizes strict adherence to safety, quality, and regulatory standards and supports long-term growth in advanced manufacturing. Job Type & Location This is a Contract position based out of Columbus, OH.
Pay and Benefits
The pay range for this position is $19.00 - $20.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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)
Job Type & Location
This is a Contract position based out of Columbus, OH.
Application Deadline
This position is anticipated to close on Nov 6, 2026.
Workplace Type
This is a fully onsite position in Columbus,OH. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability,
please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.

Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.