URGENTLY HIRING: GMP Scientist I

GMP Scientist I / GMP Operations Technician I The GMP Scientist I / GMP Operations Technician I supports all aspects of Good Manufacturing Practices (GMP) and production within a clinical manufacturing environment focused on cell-based manufacturing. This role provides hands‑on support for day‑to‑day GMP and viral vector core production operations, including execution of production processes, documentation, and facility and equipment maintenance. The position contributes directly to the timely, compliant, and cost‑effective delivery of biological products by following established batch records and Standard Operating Procedures (SOPs). This is a non‑research role that operates primarily in a GMP laboratory and clean room setting. Responsibilities Support all aspects of GMP operations and production in a clinical manufacturing facility focused on cell-based manufacturing. Execute production processes for biological products in accordance with batch records, Standard Operating Procedures (SOPs), and GMP guidelines. Provide hands‑on assistance for day‑to‑day GMP and viral vector core production operations, ensuring activities are completed accurately and on schedule. Order, receive, and maintain materials and consumables to support production goals, ensuring appropriate documentation and traceability for GMP activities. Monitor and manage inventory of GMP resources and supplies to ensure continuous availability of materials required for manufacturing. Support daily operational activities related to GMP manufacturing by verifying that materials meet quality requirements and are accompanied by proper documentation. Work closely with GMP management to identify continuous improvement opportunities using metrics and other statistical tools, and help implement process enhancements. Operate facility equipment and systems in accordance with SOPs, including routine use during production activities. Perform calibration, validation, and cleaning of facility equipment and systems as specified in SOPs to maintain a qualified and compliant state. Assist in the review, revision, and remediation of process documentation, including batch records and SOPs, to ensure accuracy and regulatory compliance. Support process change control activities by documenting proposed changes, contributing to impact assessments, and following approved implementation procedures. Spend approximately 5075% of work time in the laboratory and clean room performing hands‑on production and operational tasks. Spend approximately 25% of work time on documentation, paperwork, and preparation for upcoming production steps. Adhere strictly to aseptic techniques and GMP standards to maintain product quality and prevent contamination. Follow all safety, quality, and compliance procedures while working in laboratory and clean room environments. Occasionally lift, push, or pull materials and equipment weighing approximately 3045 pounds as part of routine operational duties. Essential Skills Experience working in aseptic processing or GMP manufacturing environments. Experience in drug compounding, drug manufacturing, food manufacturing, or other FDA‑regulated production settings. 23 years of experience in the scientific industry preferred. Knowledge and understanding of aseptic technique and its application in GMP manufacturing. Knowledge of cell culture techniques, including mammalian or eukaryotic cell culture. Understanding of liquid separation techniques relevant to biological manufacturing processes. Familiarity with tissue culture and microbiology laboratory practices. Ability to work effectively in laboratory and clean room environments for extended periods. Ability to occasionally lift, push, or pull 3045 pounds in support of production and facility operations. Strong attention to detail and adherence to documented procedures and SOPs. Demonstrated long‑term interest and desire to build a career in the science field. Additional Skills & Qualifications Associate or Bachelors degree in a science‑related discipline preferred. Prior cell‑based experience with mammalian or eukaryotic cells is a strong plus. Experience in laboratory environments involving GMP, tissue culture, cell biology, and microbiology. Comfort working in a highly regulated, documentation‑driven environment. Ability to collaborate with GMP management and cross‑functional teams to support continuous improvement initiatives. Strong organizational skills for managing inventory, materials, and documentation. Team‑oriented mindset and willingness to contribute to a growing, start‑up style operation. Adaptability to evolving processes and technologies in a state‑of‑the‑art clinical manufacturing facility. Work Environment The work environment is a highly collaborative, team‑oriented clinical manufacturing setting with a diverse group of scientific and operational professionals. The role is primarily on‑site and hands‑on, with approximately 5075% of time spent in the laboratory and clean rooms and the remainder devoted to documentation and preparation activities. The facility operates under strict GMP standards and utilizes state‑of‑the‑art equipment and systems for cell‑based manufacturing and viral vector production. Team members are on their feet for most of the day and follow established gowning procedures to enter and work in clean rooms. The dress code is casual lab attire, including closed‑toe shoes, socks covering the ankles, khaki pants or jeans without holes, and shirts without large graphics. The standard work schedule is Monday through Friday, 8:00 a.m. to 5:00 p.m., providing a stable daytime shift in a growing organization that offers strong opportunities for professional development within the scientific field. 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. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job‑related factors. 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) Application Deadline This position is anticipated to close on Nov 7, 2026. Workplace Type This is a fully onsite position in Columbus,OH. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email View email address on click.appcast.io for other accommodation options. San Francisco Fair Chance Ordinance Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI) We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools. #J-18808-Ljbffr Actalent