Additional Skills & Qualifications:

　　MUST HAVE:

　　BS degree in a life science field, biochemistry, microbiology, or virology

　　Minimum 1+ years of experience in the scientific industry from a GMP or GLP setting

　　Knowledge and understanding of aseptic technique, cell culture, liquid separation techniques and/ or fluid handling.

　　Experience with cells specifically with Mammalian or eukaryotic. This experience can be from school as long as it was hands on experience in labs.

　　Need to do more than run assays or just do routine testing

　　Chromatography experience

　　Making solutions and buffers

　　Alloguoting experience

　　Understanding/exp. with cell culture, transfections, suspension cells, or adherent cells

　　Knowledge of GMP or bioprocessing

　　PLUS:

　　Purification technique experience

　　GMP experience

　　Description:

　　The Scientist 1 is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working on collaboration with the Manager of GMP Operations and staff, 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. A Technician 1 will support production efforts to deliver all products in a timely complaint, and fiscally responsible fashion by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for Manufacturing biological products.

　　50-75% will be lab work

　　About 25%- support paperwork and getting ready for next steps in process

　　GMP- research grade production lab work, biology tissue culture based work and heavy solution prep and assay management

　　-Work in collaboration with management and staff to cultivate and enact the strategic direction of the GMP area including determination of schedule and project timelines/capabilities

　　-Supports GMP resources and supply chain including maintaining materials inventory control to meet production goals

　　-Operate and perform the calibration, validation, cleaning, of all facility equipment and systems as specified in SOPs

　　-Assist in process documentation review, revision, remediation, and process change controls

　　-Work in close collaboration with GMP Management to insure continuous improvement objectives are identified and met using metrics and other statistical means

　　-Making and developing viruses, some Pd work

　　Skills:

　　GMP, tissue, virology, biology, Cell culture, solution prep, Mammalian cell culture, Eukaryote, Pcr, Assay

　　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

　　Actalent is an equal opportunity employer.

　　About Actalent

　　Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.