QC Associate I

Job Title: Quality Control Associate IJob Description As a Quality Control Associate I, you will perform testing to develop methods for flow cytometry and analysis. You will engage in cell culture and cell counting to ensure quality control and help analyze flow methods and complexity testing. Your role will involve providing input to improve workflow and laboratory activity and offering training and oversight to new team members. Responsibilities + Execute company and client test methods and procedures of cellular products to ensure safety and efficacy. + Perform maintenance, monitoring, and troubleshooting of laboratory equipment. + Test, document, and report results for products or materials following CGMP and GTP guidelines. + Organize the lab and manage supplies efficiently. + Perform cleanings of laboratory equipment as per SOP. + Assist in equipment and method qualification/validation activities. + Cross-train in methods for multiple clients to enhance lab efficiency. + Upload data in real-time to shared drives or client SharePoint sites. + Prepare reagents and media. + Respond to equipment alarms using the Linc Alarm Report system. + Troubleshoot malfunctioning equipment and provide insights based on experience. + Investigate out-of-specification, out-of-trend, aberrant, and non-conforming test results. + Initiate, investigate, and prepare deviation reports with supervisor input. + Brainstorm and implement corrective and preventive actions. + Document training and execute shipping test samples to contract laboratories. + Complete all documentation according to SOPs in line with CGMP and GDP. + Communicate effectively with coworkers, departments, management, and clients. + Assist in training other Quality Control technicians. Essential Skills + Flow cytometry and cell culture expertise. + 1-2 years of experience in performing flow cytometry assays and endotoxin testing. + 1-2 years of cell culture experience. + Experience in quality control settings. + Proficiency in clinical and commercial production support. + Familiarity with process checkpoint, stability, and release analytical testing. Additional Skills & Qualifications + Bachelor's or Master's degree in a related scientific field. + Experience with microbiology test methods. + Experience in training and leading others in the lab. + Experience in a CGMP/GTP environment is preferred. + Prior industrial experience in cell count methodologies is preferred. + 2-4 years of experience in a Quality Control laboratory setting or the biopharmaceutical industry. + Proficiency with Microsoft Office and Visio. Work Environment This position operates on a Sun-Thurs second shift schedule from 2:30 PM to 11:00 PM. Initial training occurs Monday through Friday from 8:00 AM to 4:30 PM. Flexibility is required as work hours may vary. You will work within an aseptic quality environment, alongside scientists and other associates. The role involves electronic-based SOPs and paper-based testing and documentation. The company fosters a collaborative environment with opportunities for growth, project management, and leadership roles. Job Type & Location This is a Contract to Hire position based out of Allendale, NJ. Pay and Benefits The pay range for this position is $30.00 - $31.00/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 Allendale,NJ. Application Deadline This position is anticipated to close on Apr 30, 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: 2026-04-20