GMP Technician

Actalent; Grove City (OH); On-site; USD 28,000 - 30,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) plan

Paid time off

Training provided

Job summary

Actalent is seeking a GMP Technician to support production and quality control in a cGMP environment. This entry-level contract role focuses on following procedures, maintaining a clean workspace, and documenting activities accurately during a new product launch.

The position is based in Grove City, OH, on the 1st shift (7:00 a.m. – 3:30 p.m.) with full training and potential transition to direct hire depending on business needs.

Qualifications

• High school diploma or associate degree; bachelor’s degree not required.
• Willingness to work in a GMP cleanroom and gowning procedures.
• Basic data entry and documentation skills.
• Ability to follow standard operating procedures (SOPs) and safety rules.
• Strong attention to detail and accuracy in batch records and documentation.
• Ability to work both independently and as part of a small team.

Responsibilities

• Follow all quality and production procedures to ensure products meet cGMP standards.
• Adhere to work instructions to consistently produce products.
• Perform routine quality checks on equipment and instruments.
• Maintain safety and PPE standards; keep equipment in good order.
• Clean and maintain lab and production areas for safety and compliance.
• Complete batch documentation per GDP and quality guidelines.
• Operate basic software including Microsoft Office and QMS.

Skills

Follow SOPs

GMP cleanroom gowning

Data entry

Basic math

Attention to detail

Independent & team player

Strong documentation

Attendance reliability

Education

High school diploma or associate degree

Tools

Quality Management Systems

Microsoft Office

Job description

GMP Technician

1st shift: 7:00 a.m. to 3:30 p.m

Actalent is seeking a GMP Technician who supports production and quality control teams in manufacturing products used in cGMP operations. This entry-level role focuses on following established procedures, maintaining a clean and safe environment, and completing accurate documentation in a regulated setting. The position begins as a contract role to support a new product launch, with the potential to transition to a direct hire based on business needs and workload.

Responsibilities

• Follow all quality and production procedures to ensure that products meet cGMP standards and internal quality requirements.
• Adhere to detailed work instructions to consistently and accurately produce products for manufacturing.
• Perform routine quality checks on equipment and instruments used in production to confirm proper function and calibration.
• Comply with all required safety standards, wear appropriate personal protective equipment (PPE), and maintain production equipment in safe working order.
• Clean and maintain laboratory and production equipment, as well as the working area, to promote safety, efficiency, and regulatory compliance.
• Complete batch documentation according to local procedures, GDP requirements, and quality guidelines.
• Operate basic software applications, including Microsoft Office and Quality Management Systems, to support production and documentation activities.
• Work both independently and collaboratively with the team to achieve individual, team, and organizational goals.
• Follow established safety guidelines and protocols when working with materials that may have biohazard potential.
• Participate in documentation training and apply GLP and GMP principles to daily tasks.
• Use hand tools frequently as part of assembly, packaging, inspection, and equipment maintenance activities.
• Support lab cleanup and adherence to ISO and GMP requirements as part of routine operations.
• Maintain consistent attendance and reliability to support steady production workflows.

Essential Skills

• Ability to follow written work instructions, safety rules, operating and maintenance instructions, and standard operating procedures.
• Comfort working in and gowning up for a GMP cleanroom laboratory environment.
• Basic computer skills, including data entry and use of Microsoft Office applications.
• Ability to operate and navigate Quality Management Systems as trained.
• Capability to perform basic math required for production and documentation activities.
• Ability to perform frequent work with hand tools in a production or laboratory setting.
• Strong attention to detail for batch record completion, inspection, and quality checks.
• Ability to work independently and as part of a small team in a regulated environment.
• Commitment to maintaining good attendance and reliability.
• Understanding and application of GMP, GDP, and GLP concepts as part of daily tasks.

Additional Skills & Qualifications

• High school diploma or associate degree; a bachelor’s degree is not required for this entry-level role.
• Prior GMP or regulated industry experience is a plus but not required.
• Experience with cleanroom operations, including gowning, cleaning, and contamination control, is beneficial.
• Familiarity with packaging, assembly, labeling, inspection, and batch record processes is an advantage.
• Interest in gaining hands‑on GMP experience in a high‑demand field and developing skills in ISO and GMP documentation.
• Willingness to participate in comprehensive training with verification by experienced team members.

Work Environment

The role is based in a GMP cleanroom laboratory and production environment, where the technician gowns up and follows strict cleanliness and contamination control procedures. Standard hours are approximately 7:00 a.m. to 3:30 p.m., working five 8-hour days per week, with some flexibility for appointments as needed. The position includes a 30- to 60-minute unpaid lunch break. Full training is provided over several weeks, including documentation training, lab cleanup processes, and ISO and GMP requirements, with a second set of eyes verifying work during the learning period. The technician works alongside one other GMP Technician in a small, collaborative team setting, using basic computer systems, Quality Management Systems, and hand tools as part of daily tasks in a regulated, safety-focused environment.

Job Type & Location

This is a Contract position based out of Grove City, OH.

Pay and Benefits

The pay range for this position is $20.00 - $22.00/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)

Workplace Type

This is a fully onsite position in Grove City,OH.

Application Deadline

This position is anticipated to close on Sep 29, 2026.

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 [e-mail] 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.