Scientist I Job Description The Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). The role involves collaboration with the Manager of GMP Operations and staff, providing hands-on assistance for daily GMP production operations, including execution of production processes, documentation, and facility and equipment maintenance. The GMP Scientist I will contribute to the timely, compliant, and cost-effective delivery of products by adhering to appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products. Responsibilities + Conduct 50-75% of lab work including research-grade production, biology tissue culture-based work, heavy solution preparation, and assay management. + Support 25% of paperwork and preparations for the next steps in the process. + Collaborate with management and staff to cultivate and enact the strategic direction of the GMP area, including schedule and project timeline determination. + Maintain GMP resources and supply chain, including materials inventory control, to meet production goals. + Operate, calibrate, validate, and clean facility equipment and systems as specified in SOPs. + Assist in the review, revision, remediation, and process change control of documentation. + Work closely with GMP Management to ensure continuous improvement objectives are identified and met using metrics and statistical means. + Develop and produce viruses, including process development (Pd) work. Essential Skills + Bachelor's degree in a life science field, biochemistry, microbiology, or virology. Additional Skills & Qualifications + Experience with purification techniques. + Prior GMP experience. Pay and Benefits The pay range for this position is $24.00 - $24.00 • 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 Dublin,OH. Application Deadline This position will be accepting applications until Dec 31, 2024. 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. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are 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 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.