URGENTLY HIRING: Quality Control Technician

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 ufeff 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 operates within a regulated GMP environment and focuses on performing routine sample assays, maintaining QC laboratory equipment, and supporting method development under the guidance of senior staff. The technician helps ensure that all testing, documentation, and sample management activities comply with applicable regulatory requirements for cellular and gene therapy products. Responsibilities + Perform routine QC sample assays for viral vectors and cells, often running the same assays five nights a week to support cGMP production activities. + Work in close collaboration with senior QC staff to support the strategic direction of the GMP area and ensure alignment with quality and regulatory expectations. + Operate, calibrate, validate, clean, and maintain QC laboratory equipment according to established procedures and schedules. + Execute QC methods and assist in the development and optimization of new methods under the guidance of senior staff. + Analyze microbiological environmental monitoring samples to support clean room and facility control. + Write and revise Standard Operating Procedures (SOPs) and related documentation to reflect current practices and regulatory requirements. + Perform equipment maintenance and monitoring to ensure reliable operation and compliance with QC standards. + Manage materials for QC and Production, including ordering, tracking, and organizing supplies to support uninterrupted laboratory operations. + Ensure all product samples are adequately labeled and that sample allocation, storage conditions, and transitions are accurately documented in the appropriate formats and systems. + Maintain full accountability for product samples as they are allocated across various testing requirements and storage conditions. + Evaluate processes related to sample management, identify gaps or inefficiencies, and implement improvements in collaboration with the team. + Complete, review, file, and archive documentation in accordance with SOPs and quality system requirements. + Operate within the Quality Management System applicable to the manufacture of phase-appropriate material in the CMF. + Maintain compliance with applicable regulatory requirements for cellular and gene therapy products, including GMP, cGMP, and GLP standards. + Perform duties in accordance with established policies, procedures, and techniques, applying training and working knowledge relevant to assigned tasks. + Work under the close supervision of senior staff and leadership, incorporating feedback and guidance into daily activities. + Contribute effectively in a diverse, collaborative team environment by using clear communication and teamwork to achieve high productivity. + Participate in periodic cleaning of clean room facilities to maintain a controlled and compliant environment. + Provide periodic assistance with the manufacturing of viral vector products as needed to support production operations. + Document all activities performed accurately and in a timely manner in accordance with applicable procedures and quality standards. Essential Skills + Practical experience working in a Quality Control laboratory or similar regulated environment. + Working knowledge of cGMP, GMP, and GLP principles and their application in a laboratory or manufacturing setting. + Understanding of regulatory and documentation requirements in a GMP environment, including accurate and compliant record-keeping. + Ability to operate, calibrate, validate, clean, and maintain laboratory equipment following established procedures. + Experience with biology, virology, or molecular biology techniques relevant to QC testing of viral vectors and cells. + Strong attention to detail in sample labeling, allocation, and documentation to ensure full accountability for product. + Ability to follow SOPs, policies, and procedures precisely and consistently. + Effective communication skills to function in a diverse and collaborative team environment. + Ability to work under close supervision, accept guidance from sr staff, and apply feedback to improve performance. Additional Skills & Qualifications + Degree in Biology or another relevant science field. + Experience in a GMP manufacturing environment, highly preferred. + BG in biology, virology, molecular biology, or related research areas. + Familiarity with aseptic technique and working in clean room environments. + Experience with mammalian cell culture techniques. + Hands-on experience with PCR procedures. + Hands-on experience with ELISA procedures. + Understanding of quality control, regulatory requirements, and clean room practices. + Ability to contribute to method development and continuous improvement of sample management processes. Work Environment The role is based in a rapidly growing organization that is building two new, state-of-the-art sites in Columbus, Ohio. The work takes place primarily in modern Quality Control laboratories and advanced clean room facilities equipped with contemporary technologies and equipment for cellular and gene therapy manufacturing. Team members work in cross-functional groups that collaborate closely across QC, manufacturing, and other functions. The environment emphasizes adherence to GMP, cGMP, and GLP standards, with a strong focus on documentation, regulatory compliance, and continuous improvement. Work in clean rooms requires appropriate gowning and aseptic practices consistent with controlled facility standards. 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: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 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 Apr 27, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, weu2019ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APACu2014with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at .

Created: 2026-04-15