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). Working in collaboration with the Manager of GMP Operations and staff, the Scientist I will provide hands-on assistance for all day-to-day GMP/AAV production operations, including the execution of production processes, documentation, as well as facility and equipment maintenance. The Scientist I 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. Lots of opportunity for growth and development! Responsibilities + Work in collaboration with AAV management and staff to cultivate and enact the strategic direction of the GMP area including determination of schedule and project timelines/capabilities. + Support PD resources and supply chain including maintaining materials inventory control to meet production goals. + Perform tasks in Biosafety Cabinets. + Operate and perform the calibration, validation, and cleaning of all facility equipment and systems as specified in SOPs. + Assist in process documentation review, revision, remediation, and process change controls. + Collaborate closely with GMP Management to ensure continuous improvement objectives are identified and met using metrics and other statistical means. + Engage in making and developing viruses and some PD work. + Work with media bags and Hyperstacks, and be comfortable moving/lifting 40 lbs on occasion. Qualifications + BS degree in a scientific field, ideally in Biochemistry, Microbiology, Virology, or Genetics. + Minimum of 1+ years of experience in the scientific industry, preferably working in a GMP setting or with cells. + Knowledge and understanding of aseptic technique, cell culture, liquid separation techniques, and/or fluid handling with cells, specifically with mammalian or eukaryotic cells. + Experience with chromatography, pipetting, and centrifugation. + Experience with making solutions and buffers. 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.