Seeking a Scientist I to support a large Biotech company in Columbus, Ohio.

Hours are 7:00am-5:30pm Mon, Tues, Thurs, and Fri (4-10's, OFF Wednesdays)

Description: The Scientist I 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 and about 25%- support paperwork and getting ready for next steps in process.

+ 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

Pay:

+ 1+ years of experience: start between $23-24/hr.

+ 2+ years of experience: up to $28/hr

Qualifications:

+ BS degree in a life science field: biology, biochemistry, microbiology, or virology preferred

+ 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.

+ Chromatography experience

+ Making solutions and buffers

+ Alloquoting experience

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

+ Knowledge of GMP or bioprocessing

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 ...@actalentservices.com ( ...@actalentservices.com) for other accommodation options.