Quality Specialist II

Overview

We are looking to add a Quality Specialist II with a large Gene Therapy company in the area! This team serves as the first line of defense for whenever there's any issues in the suite/lab and some guidance might be needed.

This role handles all quality documentation and concerns before determining if an issue might need to be escalated to the Investigations team. This role does not perform any laboratory testing, and focuses more on the documentation side of things.

• Reviewing any discrepancies to see if they can be remedied, or if they need to be escalated.
• Review batch records.
• Oversee and assist with any guidance needed in the cleanroom.
• Perform various quality documentation.
• Review quality documentation to ensure it meets necessary regulations and guidelines.

• Must have a Bachelor’s Degree (preferably in a scientific field)
• Must have at least 2-3+ years of experience working in the quality department in a heavily regulated environment (GMP preferred, but would also consider GLP, FDA, or other similarly regulated environments). Must have strong documentation experience.

This is a Contract to Hire position based out of Columbus, OH.

• The pay range for this position is $28.00 - $28.00/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.

Final date to receive applications:
This position is anticipated to close on Feb 13, 2026.

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 actalentaccom for other accommodation options.