GMP Scientist I

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 processGMP- 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

Top Skills Details

GMP, tissue, virology, biology,Cell culture,solution prep

Additional Skills & Qualifications

MUST HAVE:BS degree in a life science field, biochemistry, microbiology, or virologyMinimum 1+ years of experience in the scientific industry from a GMP or GLP settingKnowledge 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 testingChromatography experienceMaking solutions and buffersAlloguoting experienceUnderstanding/exp. with cell culture, transfections, suspension cells, or adherent cellsKnowledge of GMP or bioprocessingPLUS:Purification technique experienceGMP experience

Experience Level

Intermediate Level

Pay and Benefits

The pay range for this position is $24.00 - $24.00/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

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 is anticipated to close on Jun 3, 2025.

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.

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 due to a disability, please email ... for other accommodation options.