URGENTLY HIRING: Cell And Gene Scientist I

Actalent; Columbus (OH); On-site; USD 27,000 - 39,000; Full time

Job summary

Actalent in Columbus, OH is seeking a GMP Scientist I to support day‑to‑day GMP production in the Clinical Manufacturing Facility. You will execute production processes, maintain batch records, and ensure equipment and facility compliance under the GMP Operations Manager.

This role blends hands‑on lab work (50–75%) with documentation (25%), focusing on tissue culture, solution preparation, and assay management while collaborating on scheduling and continuous improvement initiatives.

Qualifications

• BS degree in a life science (biochemistry, microbiology or virology) and GMP/GLP experience.
• Experience in GMP environments and documentation.
• Familiarity with tissue culture and virology concepts.

Responsibilities

• Execute production processes and maintain documentation per batch records and SOPs.
• Perform lab work (50-75%) and support paperwork for subsequent steps (25%).
• Conduct research‑grade production lab work focusing on biology tissue culture, solution preparation, and assay management.
• Collaborate with GMP Management to plan scheduling and timelines.
• Support GMP resources and supply chain, maintaining materials inventory.
• Operate, calibrate, validate, and clean facility equipment per SOPs.
• Assist in reviewing and updating process documentation changes.
• Work with GMP Management to drive continuous improvement using metrics.
• Develop and produce viruses and engage in product development work.

Skills

GMP

Tissue culture

Cell culture

PCR

Assay management

Documentation

Team collaboration

Continuous improvement

Education

BS degree in a life science (biochemistry, microbiology, or virology)

Tools

Chromatography

Solution preparation

Buffer preparation

Job description

GMP Scientist I

Job Description

The Scientist I plays a crucial role in supporting all aspects of Good Manufacturing Practices (GMP) and production within the Clinical Manufacturing Facility (CMF). This position involves hands‑on assistance for day‑to‑day GMP production operations, including executing production processes, maintaining documentation, and ensuring facility and equipment maintenance. The role requires working collaboratively with the Manager of GMP Operations and staff to ensure timely and compliant product delivery.

Responsibilities

• Execute production processes and maintain detailed documentation in accordance with batch records and Standard Operating Procedures (SOPs).
• Engage in lab work (50-75%) and support paperwork and preparation for subsequent process steps (25%).
• Conduct research‑grade production lab work, focusing on biology tissue culture, solution preparation, and assay management.
• Collaborate with management and staff to cultivate and implement the strategic direction of the GMP area, including scheduling and project timelines.
• Support GMP resources and supply chain management, maintaining materials inventory control to meet production goals.
• Operate, calibrate, validate, and clean all facility equipment and systems as specified in SOPs.
• Assist in reviewing, revising, remediating, and controlling process documentation changes.
• Work closely with GMP Management to identify and achieve continuous improvement objectives using metrics and statistical methods.
• Develop and produce viruses, engage in product development work.

Essential Skills

• Strong understanding of GMP, tissue, virology, biology, cell culture, and microbiology.
• Proficiency in mammalian cell culture, eukaryote handling, PCR, and assay execution.
• BS degree in a life science field such as biochemistry, microbiology, or virology.
• Minimum of 2+ years of experience in the scientific industry within a GMP or GLP setting.
• Knowledge of aseptic technique, cell culture, liquid separation techniques, and fluid handling.
• Hands‑on experience with mammalian or eukaryotic cells, including lab work during education.
• Experience with chromatography, solution making, and buffer preparation.
• Proficiency in aliquoting and understanding of cell culture, transfections, suspension cells, or adherent cells.

Additional Skills & Qualifications

• Experience in purification techniques.
• Knowledge of GMP or bioprocessing.

Work Environment

The work environment is highly team‑oriented and diverse, fostering collaboration among a growing team. Currently comprising 23 individuals, the team is set to expand significantly by the year's end. Successful candidates must excel in teamwork, as no work or testing is performed in isolation.

Job Type & Location

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

Pay and Benefits

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

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job‑related factors.

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)

Job Type & Location

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

Application Deadline

This position is anticipated to close on Nov 7, 2026.

Workplace Type

This is a fully onsite position in Columbus,OH.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.