Quality Control Scientist I

Interested candidates can send updated resumes to mamcdonough @actalentservices .com or text Marisa at 330. 397. 1302 to set up a phone interview!

Job Description

Join our dynamic Quality Department to support the testing and analysis of cGMP produced viral vectors and cells. Collaborate closely with the QC manager and senior QC staff to cultivate and enact strategic direction within the GMP area. With guidance from senior staff, engage in QC method performance and development, microbiological environmental monitoring sample analysis, SOP writing and revision, equipment maintenance and monitoring, and materials management for QC and Production supplies. Laboratory testing will encompass PCR, qPCR, ddPCR, Gel Electrophoresis, and pH measurement. Operate within the Quality Management System applicable to the manufacture of phase-appropriate material in the CMF.

Responsibilities

• Ensure all product samples are adequately labeled and document all aspects of sample allocation and transition in the respective format and systems.
• Take full accountability for product allocation across sample requirements and storage conditions.
• Evaluate processes associated with sample management to identify gaps and implement improvements.
• Complete, review, file, and archive documentation according to Standard Operating Procedures (SOPs).
• Maintain compliance with applicable regulatory requirements for cellular and gene therapy products.
• Perform tasks in accordance with established policies, procedures, and techniques, requiring training and working knowledge related to tasks performed.
• Work under close supervision of senior staff and leadership.
• Function effectively in a diverse and collaborative team environment, utilizing clear communication to deliver high productivity.
• Document all activities performed according to established guidelines.

• BS degree in Biology or another science field.
• 6 months or more of Industry Quality Experience.
• Understanding of regulatory and documentation constraints in a GMP environment.

• Prior GMP experience, report writing, and documentation review are preferred.
• Experience from GMP manufacturing is highly preferred.

The work environment is highly collaborative, with a team-oriented approach where members work closely with one another. The team size ranges from 10-12 individuals per shift, with a business casual dress code. The position is located at the Dublin ADC, operating on a flexible first shift schedule from Monday to Friday, 8:00 AM to 4:30 PM.

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 26, 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.