Quality Control Technician

Quality Control Technician

Responsibilities

• Perform QC methods and assays on cGMP-produced viral vectors and cells, including running the same assays up to five nights per week to support production needs.
• Operate within the Quality Management System applicable to the manufacture of phase-appropriate material in the clinical manufacturing facility (CMF).
• Perform proper operation, calibration, validation, cleaning, and maintenance of QC laboratory equipment in accordance with established procedures.
• Execute and assist in the development of QC methods under the guidance of experienced staff, ensuring methods are scientifically sound and compliant with regulatory expectations.
• Write, revise, and follow Standard Operating Procedures (SOPs) related to QC activities, equipment, and sample handling.
• Manage materials and supplies for QC and Production, including ordering, inventory tracking, and proper storage.
• Ensure all product samples are adequately labeled and that all aspects of sample allocation, storage conditions, and transitions are documented in the appropriate formats and systems.
• Maintain full accountability for product samples as they are allocated across different sample requirements, test panels, and storage conditions.
• Evaluate processes associated with sample management, identify gaps or inefficiencies, and implement improvements in collaboration with experienced staff.
• Ensure all documentation is completed, reviewed, filed, and archived according to SOPs and regulatory requirements.
• Maintain compliance with applicable regulatory requirements for cellular and gene therapy products in all QC activities.
• Perform tasks in accordance with established policies, procedures, and techniques, applying training and working knowledge to daily responsibilities.
• Work under close supervision of experienced staff and leadership, seeking guidance and feedback to ensure accurate and compliant execution of tasks.
• Participate as a functional member of a diverse and collaborative team, using clear and professional communication to support high productivity and shared goals.

Essential Skills

• Experience working in a Quality Control laboratory environment, preferably supporting cGMP-produced viral vectors, cells, or related biologics.
• Working knowledge of biology, virology, and molecular biology relevant to cellular and gene therapy products.
• Familiarity with cGMP requirements and quality systems in a regulated biopharmaceutical or related environment.
• Demonstrated ability to operate, calibrate, validate, clean, and maintain laboratory equipment in accordance with SOPs.
• Strong documentation skills, including accurate completion of laboratory records, logs, and forms in a regulated setting.
• Understanding of regulatory and documentation constraints in a GMP environment, including data integrity and traceability.
• Ability to follow established policies, procedures, and techniques with a high level of attention to detail.
• Capability to work effectively under close supervision, accept feedback, and apply guidance from experienced staff and leadership.
• Effective communication skills and the ability to function productively within a diverse, collaborative team.
• Bachelor's degree in Biology or another life science field, or equivalent education in a related discipline.

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 $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 Jul 3, 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 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 View email address on click.appcast.io 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.