Scientist I

Scientist I INTERESTED CANDIDATES PLEASE APPLY AND SEND RESUMES TO CARRIE AT CSTUDEBA @ OR TEXT 937. 903. 3402 TO SET UP AN INTERVIEW The Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working on collaboration 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 execution of production processes, documentation, as well as facility and equipment maintenance. A Technician 1 will support production efforts to deliver all products in a timely complaint, and fiscally responsible fashion by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for Manufacturing biological products. 50-75% will be working in the lab and clean room About 25%- support paperwork and getting ready for next steps in process THIS IS NOT A RESEARCH BASED ROLE - They are doing cell-based manufacturing in a GMP environment. Supports Plasmids resources and supply chain by ordering and maintaining materials inventory to meet production goals Supports 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, cleaning, of all facility equipment and systems as specified in SOPs Assist in process documentation review, revision, remediation, and process change controls Additional Skills & Qualifications MUST HAVE: - Bachelors or Master's in Life Science Field - Prefer - Experience in Drug Compounding, Drug Manufacturing, Food Manufacturing/FDA - GMP or GLP exp. - Prior cell based experience (either mammalian cell or eukaryotic cell) is preferred - Knowledge and understanding of aseptic technique, cell culture, liquid separation techniques - Long term interest and desire to be Cell/Gene Therapy - Experience leading projects and developing others preferred - Must be comfortable occasionally lifting/pushing/pulling 30lbs Hours: 1st shift position Mon-Fri, but depending on the position/team (there are multiple openings) MUST be flexible to changes in schedule. Some days will require OT, some holidays, weekends, heavily varied. 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: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 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 20, 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 ( ) for other accommodation options.

Created: 2026-03-09