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Lab Tech

Job in Frederick, Frederick County, Maryland, 21701, USA
Listing for: The Fountain Group
Full Time position
Listed on 2026-07-28
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 21.9 USD Hourly USD 21.90 HOUR
Job Description & How to Apply Below
Position: Lab Tech - I*

The Fountain Group is currently seeking a Quality Control Technician I for a prominent client of ours. This position is located in Frederick, MD . Details for the position are as follows:

Job Title:

Quality Control Technician I - QC Lab Support

Location:

100% Onsite (Lab Environment)

Pay Rate:

$21.90/hr (W2)

Duration:

1 Year (Ongoing Temp)

Job Description
  • Receive, verify, and log incoming samples into LIMS.
  • Process, aliquot, label, store, and organize samples for release, stability testing, and retains.
  • Coordinate sample transfers to internal and external testing laboratories.
  • Perform sample shipping activities and maintain chain of custody documentation.
  • Maintain sample storage areas through routine cleaning, maintenance, and inventory support.
  • Review QC Lab Support records, processing logs, and documentation.
  • Support deviation investigations and Operational Excellence (Lean Lab) initiatives.
  • Collaborate with QC, QA, Manufacturing, Analytical Development, Material Management, and Corporate QC to support testing and sample management.
  • Ensure compliance with GMP, safety, and regulatory requirements.
Education
  • Bachelor's degree OR
  • Associate's degree with 2+ years of Quality Control or biopharmaceutical laboratory experience OR
  • High School diploma with 3+ years of Quality Control or biopharmaceutical laboratory experience in an FDA-regulated environment.
Required Skills
  • Quality Control laboratory experience
  • Sample management and sample processing
  • LIMS (Laboratory Information Management System)
  • Sample aliquoting and storage
  • Sample shipment and chain of custody
  • GMP in QC laboratory
  • FDA-regulated laboratory experience
  • QC documentation and record review
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