Plasmids Scientist I

Job Description

Plasmids Scientist I

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 Plasmids R&D Scientist I will support all aspects of Good Manufacturing Practices (GMP) and production within Clinical Manufacturing (CMF). Collaborating with the Manager of GMP and Plasmids Operations and staff, the role involves hands-on assistance for day-to-day Plasmids Core production operations, including production process execution, documentation, and facility and equipment maintenance.

Responsibilities

Conduct testing including cell growth, chromatography, microbiological testing, and assay development.

Identify and coordinate the development of experiments to fill knowledge gaps.

Perform research and development for the production and purification of plasmids.

Anticipate and troubleshoot issues with operations to avoid production interruptions.

Collaborate with management to answer client questions regarding their product.

Ensure the availability of materials and proper documentation for GMP activities and product quality.

Operate within the Quality Management System for phase-appropriate material manufacture in the CMF.

Maintain compliance with regulatory requirements for cellular and gene therapy products.

Document all activities according to SOPs.

Support GMP resources and supply chain by managing materials inventory to meet production goals.

Assist in process documentation review, revision, remediation, and process change controls.

Solve, correct, and prevent problems, and perform tasks as assigned by leadership.

Essential Skills

Experience with GMP, tissue culture, cell biology, molecular biology, and microbiology.

Proficiency in assay development, biology, and mammalian or eukaryotic cell culture.

Bachelor's degree in a Biological Field (Biology, Biochemistry, Microbiology, Molecular, or Genetics).

Industry experience in Aseptic Processing or GMP.

Experience in Drug Compounding, Drug Manufacturing, or Food Manufacturing/FDA.

Knowledge and understanding of aseptic technique, cell culture, and liquid separation techniques.

Additional Skills & Qualifications

Prior experience with mammalian or eukaryotic cells is a big plus.

Ability to occasionally lift/push/pull 30-45 lbs.

Work Environment

The work culture is team-oriented and diverse, fostering growth. The role involves standing most of the day and requires gowning up to enter clean rooms. The dress code is casual lab attire (closed-toe shoes, socks covering ankles, khaki pants or jeans without holes, shirts without large graphics). Approximately 50-75% of the time will be spent in the lab, with the remaining time at a desk for documentation and report writing. Work hours are Monday to Friday, 8 AM to 5 PM with OT!

Job Type & Location

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

Pay and Benefits

The pay range for this position is $24.00 - $24.00/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 Nov 23, 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 for other accommodation options.