GMP Laboratory Technician

Job Description

Job Description

Job Title: GMP Laboratory Technician

INTERESTED CANDIDATES CAN SEND UPDATE RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW!

Job Description

The GMP Operations Technician 1 plays a crucial role in supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility. Collaborating with the Manager of GMP Operations and staff, the Technician will provide hands-on assistance for all day-to-day GMP and Viral Vector Core production operations, including executing production processes, documentation, as well as facility and equipment maintenance. The Technician will support production efforts to deliver all products in a timely, compliant, and fiscally responsible manner by adhering to appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products.

Responsibilities

• Support GMP resources and supply chain by ordering and maintaining materials inventory to meet production goals.
• Support daily operational activities related to the GMP manufacturing of biological products by ensuring the availability of materials with proper documentation surrounding GMP activities.
• Work closely with GMP management to ensure continuous improvement objectives are identified and met using metrics and other statistical means.
• Operate and perform the calibration, validation, and cleaning of all facility equipment and systems as specified in SOPs.
• Assist in process documentation review, revision, remediation, and process change controls.

Essential Skills

• Experience in GMP, tissue culture, biology, cell culture, microbiology, mammalian and eukaryotic systems.
• 1-2 years of experience in the scientific industry is preferred.
• Comfortable with occasionally lifting/pushing/pulling 30-45lbs.

Additional Skills & Qualifications

• Associate degree in Science is preferred.
• Experience in Aseptic Processing or GMP is required.
• Experience in Drug Compounding, Drug Manufacturing, Food Manufacturing/FDA is advantageous.
• Long-term interest and desire to be in the Science Field.

Work Environment

The work environment is team-oriented and diverse, with strong growth opportunities as the team moves into a new state-of-the-art facility. Most of the day will be spent on feet, with gowning up required for clean room access. The dress code is casual lab attire, including closed-toed shoes, socks covering ankles, khaki pants or jeans without holes, and shirts without large graphics. The shift is Monday to Friday, from 7:00 AM to 5:30 PM, with flexibility for scheduling adjustments as needed.

Pay and Benefits

The pay range for this position is $22.00 - $22.00/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 Columbus,OH.

Application Deadline

This position is anticipated to close on Aug 10, 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 [email protected] for other accommodation options.