Plasmid Scientist I

Scientist I (Plasmids)

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

Job Description

The Plasmids Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). Collaborating with the Manager of Plasmids Operations and staff, the Scientist I will provide hands-on assistance for all day-to-day Plasmid Core production operations, including the execution of production processes, documentation, as well as facility and equipment maintenance. This position supports production efforts to deliver all products in a timely, compliant, and fiscally responsible fashion by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products.

Responsibilities

• Support Plasmids resources and supply chain by ordering and maintaining materials inventory to meet production goals.

• Ensure 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 Plasmids 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 with GMP, tissue culture, cell culture, microbiology, and molecular biology.

• Proficiency in techniques such as ELISA and understanding of aseptic techniques, cell culture, and liquid separation techniques.

• Bachelor's or Master's degree in a Life Science field.

Additional Skills & Qualifications

• Experience in drug compounding, drug manufacturing, or food manufacturing with FDA-GMP or GLP experience is preferred.

• Prior cell-based experience, either mammalian or eukaryotic cells, is preferred.

• Long-term interest and desire to be involved in Cell/Gene Therapy.

• Experience leading projects and developing others is preferred.

• Must be comfortable occasionally lifting, pushing, or pulling up to 30 lbs.

Work Environment

The work culture is very team-oriented, composed of a diverse group of individuals who are continuing to grow. Employees will spend 50-75% of their time working in the lab and clean room, with about 25% of the time supporting paperwork and preparing for the next steps in the process. The dress code is casual lab attire, including closed-toed shoes, socks covering ankles, khaki pants or jeans without holes, and shirts without large graphics. The shift is Monday through Friday, from 8 AM to 5 PM.

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 Mar 19, 2026.

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 [email protected] (%[email protected]) for other accommodation options.