URGENTLY HIRING: Quality Control Technician

Job Description

Job Description

Quality Control Technician

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP AN IMMEDIATE PHONE INTERVIEW!



Job Description

The Quality Control Technician works primarily in the Quality Control Laboratory to support the testing and analysis of cGMP-produced viral vectors and cells. This role focuses on executing routine and complex QC assays, maintaining high documentation standards, and supporting a robust Quality Management System for cellular and gene therapy products. The technician collaborates closely with senior QC staff to ensure compliant operations, continuous improvement of sample management processes, and reliable delivery of high-quality data that supports manufacturing activities.

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 senior staff, ensuring methods are scientifically sound and compliant with regulatory expectations.
• Analyze microbiological environmental monitoring samples and accurately document and report results.
• Write, revise, and follow Standard Operating Procedures (SOPs) related to QC activities, equipment, and sample handling.
• Support equipment maintenance and monitoring activities, ensuring equipment remains in a qualified and operational state.
• 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 senior 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 senior 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.
• Assist periodically with cleaning of cleanroom facilities to support a controlled and compliant manufacturing environment.
• Provide periodic assistance with manufacturing of viral vector products as needed to support cross-functional operational demands.

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 sr 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.

Additional Skills & Qualifications

• Experience with aseptic technique in a laboratory or manufacturing environment.
• Hands-on experience with PCR methods and workflows.
• Experience performing ELISA procedures for analytical testing.
• Prior experience in GMP manufacturing or strong documentation experience in a regulated environment.
• Familiarity with environmental monitoring and microbiological testing in controlled environments.
• Experience contributing to the writing, reviewing, or revising of SOPs and other controlled documents.
• Ability to evaluate and improve sample management processes, including labeling, allocation, and storage practices.
• Comfort working in cross-functional teams that include QC, production, and other operational groups.
• Flexibility to adapt to evolving processes, new technologies, and the needs of a growing organization.

Work Environment

The role is based in a rapidly growing organization that is establishing new, state-of-the-art facilities in Columbus, Ohio. The Quality Control Technician works in modern cleanrooms and laboratories equipped with advanced technologies and equipment designed for cellular and gene therapy manufacturing. The environment is highly regulated and process-driven, with strong emphasis on cGMP compliance, documentation accuracy, and adherence to SOPs. Team members work in cross-functional groups that include QC, manufacturing, and other operational functions, fostering collaboration and shared ownership of quality and production outcomes. This position follows a second-shift schedule, Monday through Friday from 2:00 p.m. to 10:30 p.m., with the expectation of flexibility to work beyond 10:30 p.m. when testing demands and sample volumes require extended coverage. The work involves routine use of cleanroom garments and appropriate laboratory attire to maintain a controlled environment and ensure product and personnel safety.

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

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)

This is a fully onsite position in Columbus,OH.

This position is anticipated to close on Jul 9, 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 [email protected] 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.