GMP Scientist II

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP AN IMMEDIATE PHONE INTERVIEW!



Job Description

The GMP Scientist II is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). The role involves providing hands-on assistance for day-to-day GMP production operations, including execution of production processes, documentation, and maintenance of facilities and equipment. The scientist will ensure timely, compliant, and fiscally responsible delivery of products by adhering to batch records and Standard Operating Procedures (SOPs) for manufacturing biological products.

Responsibilities

Collaborate with management and staff to cultivate and enact the strategic direction of the GMP area, including schedule and project timeline determination.Support GMP resources and supply chain by maintaining materials inventory control to meet production goals.Operate, calibrate, validate, and clean all facility equipment and systems as specified in SOPs.Assist in process documentation review, revision, remediation, and process change controls.Work closely with GMP Management to ensure continuous improvement objectives are identified and met using metrics and statistical means.Engage in making and developing viruses and some process development work.

Essential Skills

Proficiency in GMP, tissue, virology, biology, cell culture, solution preparation, microbiology, tissue culture, mammalian cell culture, PCR, assay, and molecular biology.BS or Master's degree in a life science field such as biochemistry, microbiology, or virology.Minimum of 2-3 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 fluid handling.Hands-on experience with mammalian or eukaryotic cells in a lab setting, including school experience.Experience in solution preparation, chromatography, making solutions and buffers, aliquoting, and understanding cell culture, transfections, suspension cells, or adherent cells.Knowledge of GMP or bioprocessing.

Additional Skills & Qualifications

Experience with purification techniques.

Work Environment

The work culture is highly team-oriented, with a diverse group of 23 individuals that is expected to grow significantly by the end of the year. Collaboration is essential, as tasks and testing cannot be completed alone

Job Type & Location

This is a Contract to Hire position based out of Dublin, OH.

Pay and Benefits

The pay range for this position is $28.00 - $28.00/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 Feb 23, 2026.

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 actalentaccommodation@actalentservices.com for other accommodation options.