QC Associate I

Job Description

Job Description

Exciting opportunity with one of the fastest growing Cell & Gene Therapy companies on the East Coast!

Job Title: Quality Control Associate I

Job Description

The Quality Control Associate I will play a vital role in ensuring the safety and efficacy of cell populations by performing testing, analysis, and quality control activities. This role involves developing methods for flow cytometry, conducting cell culture and cell counting, and providing input for workflow improvements.

Responsibilities

• Perform testing to develop methods for flow cytometry and analysis.
• Conduct cell culture and cell counting for quality control purposes.
• Assist in analysis for flow methods and complexity testing.
• Provide training and oversight to new team members.
• Execute company and client test methods and procedures for cellular products.
• Maintain, monitor, and troubleshoot laboratory equipment.
• Document and report results following company and client procedures and guidelines.
• Organize laboratory supplies and perform equipment cleaning as per SOP.
• Participate 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 as needed.
• Respond to equipment alarms using the Linc Alarm Report system.
• Investigate out-of-specification, out-of-trend, or non-conforming test results.
• Initiate and prepare deviation reports with supervisory input.
• Implement corrective and preventive actions as applicable.
• Complete documentation according to SOPs, CGMP, and GDP.
• Communicate effectively with coworkers, departments, management, and clients.
• Assist in training other Quality Control technicians.

Essential Skills

• 1-2 years of experience in performing flow cytometry assays and endotoxin testing.
• 1-2 years of cell culture experience.
• Experience with test methodology within a quality control setting.
• Proficiency in aseptic techniques, assay, and document control.
• Experience in a CGMP/GTP environment.
• Proficiency with computer software such as Microsoft Office and Visio.
• Bachelor's or master's degree in a related scientific field.

Additional Skills & Qualifications t.

• Experience in tissue culture, bioburden, PCR, and quantitative analysis.
• Experience in clinical laboratories, microbiology, hematology, blood banking, or immunology.
• Prior industrial experience in cell count methodologies and cell therapeutic experience.

Work Environment

• This position operates on the 2nd shift, Sunday to Thursday, from 2:30 PM to 11:00 PM.
• Training occurs Monday to Friday from 8:00 AM to 4:30 PM.
• The role requires flexibility to accommodate potential delays in cell and gene therapy processes.
• The work environment is aseptic and quality-driven, requiring collaboration with the Analytical Team, scientists, and associates.

Job Type & Location

This is a Contract to Hire position based out of Mahwah, NJ.

Pay and Benefits

The pay range for this position is $30.00 - $32.00/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 Mahwah,NJ.

Application Deadline

This position is anticipated to close on Nov 21, 2025.

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 [email protected] for other accommodation options.