Scientist II

We are hiring for a Scientist II that will work in a cleanroom laboratory helping to manufacture Gene Therapy products. This is a long-term career opportunity for someone looking to grow in the industry

Candidates must have a Bachelors or Masters Degree in a scientific field and at least 2+ years of industry experience in a highly regulated lab. Experience following GMP regulations would be preferred, but not required. This will be largely cell based laboratory work, so experience working with mammalian or eukaryotic cells would also be preferred.

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

Job Description

The Scientist II is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). This role involves collaborating with the Manager of GMP Operations and staff to provide hands-on assistance for day-to-day GMP production operations, including executing production processes, documentation, as well as facility and equipment maintenance.

Responsibilities

• Engage in lab work focusing on biology tissue culture-based work, and heavy solution preparation. This role will be solely focused on performing cell based work to actually manufacture the product, this role does not perform any actual research.
• 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.
• Collaborate with management and staff to cultivate and enact the strategic direction of the GMP area, including the determination of schedule and project timelines/capabilities.
• Maintain GMP resources and supply chain, including materials inventory control, to meet production goals.
• 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.
• Collaborate closely with GMP Management to ensure continuous improvement objectives are identified and met using metrics and other statistical means.
• Participate in virus making and development, including some pilot development work.

Qualifications

• Bachelor's or Master's degree in a life science field
• Minimum of 2+ years of experience in the scientific industry from a highly regulated setting (preferably GMP, GLP, FDA, or similarly regulated facilities)
• Knowledge and understanding of aseptic technique, cell culture, liquid separation techniques, and/or fluid handling preferred.
• Experience with mammalian or eukaryotic cells preferred.

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

The pay range for this position is $33.00 - $33.00/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)

This is a fully onsite position in Columbus,OH.

This position is anticipated to close on Mar 23, 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 ... for other accommodation options.