Gene Therapy Laboratory Technician

The Technician is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working in collaboration with the Manager of GMP Operations and staff, the Technician will provide hands-on assistance for all day-to-day GMP & Viral Vector Core production operations, including execution of 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 following 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 assuring the availability of materials with the 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 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.
• Strong knowledge in GMP, tissue culture, biology, cell culture, microbiology, mammalian, eukaryotic, and cell biology.

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 Apr 11, 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.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

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 actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $22