Columbus, Ohio, USA
9 hours ago
GMP Laboratory Technician
Job Title: GMP Laboratory Technician
Job Description

The GMP Operations Technician 1 is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). Collaborating with the Manager of GMP Operations and staff, the Technician 1 will provide hands-on assistance for all day-to-day GMP and Viral Vector Core production operations, including the execution of production processes, documentation, as well as facility and equipment maintenance. The role involves supporting 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.

ResponsibilitiesSupport GMP resources and supply chain by ordering and maintaining materials inventory to meet production goals.Ensure the availability of materials with the proper documentation for GMP activities.Collaborate closely with GMP management to identify and meet continuous improvement objectives using metrics and statistical methods.Operate and perform 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 SkillsExperience working in Aseptic Processing or GMP.Experience in Drug Compounding, Drug Manufacturing, or Food Manufacturing/FDA.1-2 years of experience in the scientific industry preferred.Comfortable occasionally lifting/pushing/pulling 30-45 lbs.Additional Skills & QualificationsPrefer Associates in Science.Long-term interest and desire to be in the Science Field.Work Environment

The work environment is highly team-oriented and diverse, with a group of individuals that is continually growing. Technicians will spend 50-75% of their time working in the lab and clean room, with about 25% supporting paperwork and preparing for the next steps in the process. This is a non-research-based role focusing on cell-based manufacturing in a GMP environment. Dress code is casual lab attire, which includes closed-toed shoes, socks covering ankles, khaki pants or jeans with no holes, and shirts with no large graphics. Shift work is Monday to Friday, 7 AM to 5:30 PM, with a 4-day work week consisting of 10-hour shifts (Monday, Tuesday, Thursday, Friday), with some flexibility in scheduling.

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 9, 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 actalentaccommodation@actalentservices.com for other accommodation options.

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