Job Description

GMP Scientist I

INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM

OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. 980. 5823

Job Description

The GMP Scientist I is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production within the Clinical Manufacturing Facility (CMF). This role requires collaboration with the Manager of GMP Operations and staff to provide hands-on assistance with day-to-day GMP production operations, including the execution of production processes, documentation, and facility and equipment maintenance. The GMP Scientist I will contribute to delivering products in a timely, compliant, and fiscally responsible manner by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products.

Responsibilities

• Work on 50-75% lab work and 25% support paperwork and preparation for next steps in the process.

• Conduct GMP research-grade production lab work, including biology tissue culture-based work and heavy solution preparation and assay management.

• Collaborate with management and staff to cultivate and enact the strategic direction of the GMP area, including determination of schedule and project timelines/capabilities.

• Support GMP resources and supply chain by maintaining materials inventory control to meet production goals.

• 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.

• Involvement in making and developing viruses, and some Pd work.

Essential Skills

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

• Minimum of 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 Mammalian or eukaryotic, which may include hands-on lab experience from school.

• Experience beyond running assays or routine testing, including chromatography, solution and buffer preparation, and aliquoting.

• Understanding and experience with cell culture, transfections, suspension cells, or adherent cells.

• Knowledge of GMP or bioprocessing.

Additional Skills & Qualifications

• Purification technique experience.

• Additional GMP experience.

Work Environment

The work environment is very team-oriented and diverse, consisting of a group of individuals that is continuing to grow. The team currently has 23 people and is expected to expand significantly by the end of the year. Collaboration is crucial, as no work or testing is done alone. The culture promotes teamwork and mutual support among colleagues.

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 Apr 14, 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.

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.

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