Laboratory Technician - Sample Management

VARITE is looking for a qualified Quality Control Technician I - QC Lab Support in Frederick, MD.

An American biotechnology company that develops cancer immunotherapy products with a primary focus on genetically engineered autologous CAR T cell therapy – a cell-based therapy which relies on chimeric antigen receptors and T cells.

Established in 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non‑technical staff augmentation and talent acquisition services.

Quality Control Technician I – QC Lab Support

Frederick, MD (Onsite – lab environment)

12 months (possible extension)

$20.00/hr to $21.58/hr on W2

Only USC or GC

4 days × 10 hours per day;
Sun‑Wed. 7:00 am – 6:00 pm (1 opening)

The team operates 7 days a week, with an extended, overlapping shift structure.

• Execute tasks associated with sample management, shipment of samples, and other lab support QC functions, while interacting cross‑functionally with personnel from other QC groups, Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), and corporate teams.

• Receive incoming samples, verify documentation, and log sample information into LIMS.
• Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
• Label, store, and organize samples according to established procedures and storage requirements.
• Coordinate sample transfers to internal and external testing labs.
• Perform routine cleaning, maintenance, and restocking of sample storage areas.
• Collaborate with MM, QA, and other QC functions, including Corporate QC, to support requirements around sampling, testing, and disposition.
• Manage and complete all shipping activities within QC functions.
• Complete routine review of records, such as sample chain‑of‑custody forms, processing logs, logbooks, and other documentation generated within QC Lab Support.
• Assist with deviation and investigation activities as needed.
• Provide updates during daily and weekly meetings.
• Participate in Lean Lab and other operational excellence initiatives.
• Comply with all safety, quality, and regulatory guidelines.
• Perform other duties as assigned.

• Bachelor’s Degree or
• AA Degree and 2+ years’ experience working in Quality Control or biopharma laboratories preferably in an FDA‑regulated laboratory
• High School Degree and 3+ years’ experience working in Quality Control or biopharma laboratories preferably in an FDA‑regulated laboratory.

• Strong knowledge in applying GMP in QC lab.
• Exceptional attention to detail and ability to keep track of multiple ongoing projects.
• Proficient in Microsoft Office, Excel, Visio, and other related applications.
• Excellent interpersonal, verbal and written communication skills which are essential in this collaborative work environment.
• Comfortable in a fast‑paced small company environment and able to adjust workload based on changing priorities.
• Ability to be flexible with schedule, and work overtime as needed.

• Health Insurance:
  Medical, dental, and vision coverage.
• Retirement Plans:
  Participation in a company‑sponsored retirement savings plan.
• Legal Service Plans:
  Offering access to attorneys for legal advice and representation.

VARITE is committed to creating a diverse environment and is proud to be an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.