Job Title: GMP Scientist IJob Description The Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working in collaboration with the Manager of GMP Operations and staff, you will provide hands-on assistance for all day-to-day GMP production operations, including execution of production processes, documentation, as well as facility and equipment maintenance. You will support production efforts to deliver all products in a timely, compliant, and fiscally responsible manner by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products. 50-75% of the role involves lab work, with about 25% supporting paperwork and preparing for the next steps in the process. Responsibilities include GMP research-grade production lab work, biology tissue culture-based work, heavy solution prep, and assay management. Key duties include collaborating with management and staff to set the strategic direction of the GMP area, supporting GMP resources and supply chain by maintaining materials inventory control, operating and performing calibration, validation, and cleaning of all facility equipment and systems as specified in SOPs, assisting in process documentation review, revision, remediation, and process change controls, and working closely with GMP Management to ensure continuous improvement objectives are met using metrics and other statistical means. The role also involves making and developing viruses, and some process development work. Hard Skills + microbiology + tissue culture Soft Skills + collaboration + attention to detail + continuous improvement Job Type This is a Contract-to-Hire position with a duration of 6 Month(s). Work Site This is a fully on-site position in Dublin, Ohio. Work Environment The culture is very team-oriented. It is a diverse group of individuals that is continuing to grow. The team currently consists of 23 people and is looking to expand significantly by the end of the year. You must be able to work well with others, as no work or testing can be done alone. 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.