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Job Title: Scientist I (Plasmids)Job Description The Scientist I (Plasmids) supports all aspects of GMP plasmid production within a clinical manufacturing environment. This role focuses on hands-on execution of cell-based manufacturing processes, meticulous documentation, and routine facility and equipment maintenance to ensure reliable delivery of high-quality biological products. The Scientist I contributes to day-to-day plasmid core operations, follows batch records and Standard Operating Procedures (SOPs), and helps maintain a compliant, efficient, and continuously improving manufacturing operation. Responsibilities + Execute day-to-day plasmid core production operations in a GMP clinical manufacturing environment, following established batch records and SOPs. + Support cell-based manufacturing processes for biological products, ensuring activities are compliant, timely, and fiscally responsible. + Order, track, and maintain materials and consumables to support plasmid production goals, ensuring adequate inventory levels. + Ensure all materials used in GMP manufacturing are appropriately documented and meet quality and regulatory requirements. + Perform routine operation, calibration, validation, and cleaning of facility equipment and systems in accordance with SOPs. + Assist in reviewing, revising, and remediating process documentation, including batch records, SOPs, and related controlled documents. + Support implementation of process change controls by following established procedures and documenting changes accurately. + Collaborate closely with plasmids management to identify and achieve continuous improvement objectives using metrics and other statistical tools. + Contribute to the preparation of documentation and materials for upcoming production steps, including paperwork and process readiness activities. + Adhere to aseptic techniques and cleanroom procedures while working in the lab and cleanroom environment. + Maintain accurate, complete, and legible records of all manufacturing and equipment activities in compliance with GMP requirements. + Follow all safety, quality, and compliance guidelines while working with cell-based systems and biological materials. + Participate in team-based activities to support a collaborative, growth-oriented culture within the manufacturing group. Essential Skills + Bacheloru2019s or Masteru2019s degree in a Life Science field (such as biology, microbiology, cell biology, molecular biology, or a related discipline). + Experience or strong familiarity with GMP or GLP environments, preferably in drug compounding, drug manufacturing, or food manufacturing regulated by the FDA. + Understanding of cell-based manufacturing processes, with prior experience working with mammalian or eukaryotic cells preferred. + Knowledge and practical understanding of aseptic technique and cleanroom practices. + Experience or coursework in cell culture and tissue culture techniques. + Familiarity with liquid separation techniques used in biological manufacturing. + Exposure to core laboratory and biological techniques such as molecular biology assays and ELISA. + Ability to follow detailed SOPs, batch records, and documentation requirements in a regulated environment. + Capability to occasionally lift, push, or pull up to 30 pounds as part of routine duties. + Strong attention to detail, organization, and documentation skills in a GMP setting. + Demonstrated interest in cell and gene therapy as a long-term career focus. Additional Skills & Qualifications + Prior hands-on experience in drug compounding, drug manufacturing, or food manufacturing in an FDA-regulated environment. + Experience working in GMP or GLP laboratories, including familiarity with regulatory expectations and quality systems. + Previous experience with mammalian or eukaryotic cell culture in an academic, clinical, or industrial setting. + Experience leading projects or mentoring and developing others within a lab or manufacturing team. + Background in tissue culture, microbiology, and cell biology techniques. + Experience with molecular biology methods and immunoassays such as ELISA. + Comfort working in a start-up style, growth-oriented environment with evolving processes. + Strong communication skills and ability to collaborate effectively with cross-functional teams. + Motivation to build a career in cell and gene therapy manufacturing and to grow with an expanding organization. Work Environment This role is based in a GMP clinical manufacturing setting with a strong focus on cell-based manufacturing rather than research. Approximately 50u201375% of the time is spent working in the lab and cleanroom, performing hands-on manufacturing activities, while about 25% is dedicated to documentation, paperwork, and preparing for upcoming process steps. The team operates in a highly collaborative, team-oriented culture within a diverse and growing group. The organization is in a dynamic, start-up phase with the support of a larger institution and is moving into a new, state-of-the-art facility located within a research-focused campus. Team members are on their feet for most of the day and regularly gown to enter cleanrooms, following strict aseptic and GMP procedures. The dress code consists of casual lab attire, including closed-toe shoes, socks covering the ankles, khaki pants or jeans without holes, and shirts without large graphics, with additional gowning requirements when entering controlled areas. The standard work schedule is Monday through Friday, 8:00 a.m. to 5:00 p.m. 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 May 8, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, weu2019ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APACu2014with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at .