Laboratory Technologist

The Laboratory Technologist performs all laboratory procedures in a prompt, accurate, and reliable manner according to established policies and procedures. The primary responsibility is to perform specimen preparation and clinical test analyses to acceptable levels of analytic performance under the direction of the Laboratory Supervisor or Laboratory Manager in a CLIA certified laboratory.

• Accession clinical/commercial samples, barcode, and enter essential data onto a cloud-based HIPAA-compliant patient management platform.
• Process clinical samples from a variety of sources including human tissues, blood, and urine, as part of a highly cooperative team.
• Enter necessary data into a Laboratory Information Management System (LIMS) to ensure precise sample tracking and full inventory control of reagents.
• Participate in monthly Quality Management Systems (QMS) meetings and present activities and metric outcomes.
• Develop and implement remedial activity plans and suggest quality improvements.
• Maintain proficiency in the laboratory’s Standard Operating Procedures (SOPs) for clinical testing and understand quality control parameters.
• Provide hands-on back-up support to other laboratory personnel in operational clinical tests.
• Maintain laboratory records, including records for proficiency testing samples.
• Adhere to the laboratory’s quality control policies and document all quality control activities, instrument and procedural calibrations, and maintenance performed.
• Document corrective actions taken when test systems deviate from established performance specifications.
• Maintain a clean and safe work environment.
• Understand and comply with all laboratory policies and procedures.

• Bachelor of Science Degree in Biology, Biochemistry, Chemistry or Medical Technology from an accredited college or university.
• 2-3 years of experience in a clinical/commercial laboratory environment preferred.
• Experience in molecular biology methodologies, particularly RT-PCR.
• ASCP certification preferred.

• Clear understanding of patient confidentiality, as outlined in HIPAA.
• Familiarity with RNA extraction, cDNA synthesis, and Polymerase Chain Reaction (PCR)-based methodologies.
• Proficiency in basic laboratory skills (solution preparation, pipetting with single and multichannel pipettes, and robotic liquid handlers).
• Familiarity with MS Word, MS Excel, and Laboratory Inventory Management Systems.
• Excellent problem-solving skills and effective verbal and written communication skills.
• Ability to work collaboratively, exercise good judgment, and maintain clear records.

The work is performed onsite in a laboratory environment with some shift work required. The role involves medium work of lifting up to 50 pounds and carrying objects weighing up to 25 pounds. The schedule may be either Monday to Friday or Tuesday to Saturday, with flexibility for weekends preferred.

This is a Contract position based out of North Brunswick, NJ.

The pay range for this position is $25.00 - $25.00/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 North Brunswick,NJ.

This position is anticipated to close on Mar 18, 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 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 actalentaccommodation@actalentservices.com for other accommodation options.