Quality Control Technician

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

The individual will work primarily in the Quality Control Laboratory to support the testing and analysis of cGMP produced viral vectors and cells. Collaboration with the QC manager and senior QC staff is crucial to cultivate and enact strategic direction to the GMP area. The role involves running sample assays five nights a week, and performing proper operation, calibration, validation, cleaning, and maintenance of QC lab equipment.

Responsibilities

• Perform QC methods, develop methods, analyze microbiological environmental monitoring samples.
• Write and revise SOPs, maintain and monitor equipment, and manage QC and production supplies.
• Periodically clean the clean room facility and assist with manufacturing of viral vector products.
• Operate within the Quality Management System applicable to the manufacture of phase-appropriate material.
• Ensure all product samples are adequately labeled and documented.
• Account for product allocation across sample requirements and storage conditions.
• Evaluate sample management processes, identify gaps, and implement improvements.
• Complete, review, file, and archive documentation according to SOPs.
• Maintain compliance with regulatory requirements for cellular and gene therapy products.
• Perform tasks according to established policies, procedures, and techniques, under close supervision.
• Work in a diverse and collaborative team environment, utilizing clear communication for high productivity.

• Degree in Biology or other life science field.
• Experience in aseptic technique, PCR, and ELISA procedures.
• Understanding of regulatory and documentation constraints in a GMP environment.

• Experience from GMP manufacturing or strong documentation experience is highly preferred.

This role is based in a quickly growing company building two new sites in Columbus, Ohio, featuring state-of-the-art clean rooms and equipment. The work involves cross-functional teams. The shift is from Monday to Friday, 2 PM to 10:30 PM, with flexibility needed to occasionally work past 10:30 PM depending on sample testing requirements.

The pay range for this position is $22.00 - $22.00/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 Columbus,OH.

Application Deadline

This position is anticipated to close on Jun 25, 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.