More jobs:
Quality Control Technician I, QC Lab Support (Sample Management / LIMS
Job in
Jefferson, Frederick County, Maryland, 21755, USA
Listed on 2026-08-06
Listing for:
Pyramid Inc.
Full Time
position Listed on 2026-08-06
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, Production QC/QA, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Location: Jefferson
Quality Control Technician I, QC Lab Support (Sample Management / LIMS)
Immediate need for a talented Quality Control Technician I, QC Lab Support (Sample Management / LIMS). This is a 06+ months contract opportunity with long-term potential and is located in Fredrick, MD (Onsite).
Pay Range: $20 - $21/hour. Traveler benefits as per agency package. (Benefits vary by vendor and assignment.)
Key Responsibilities:- Receive incoming samples, verify documentation, and accurately log sample data into LIMS.
- Support sample receipt, processing, aliquoting, and organization for release testing, stability testing, and retains.
- Label, store, and maintain samples according to established procedures and storage requirements.
- Coordinate sample transfers to internal and external testing laboratories.
- Manage shipping activities within QC functions.
- Perform routine cleaning, maintenance, organization, and restocking of sample storage areas.
- Review QC laboratory records including chain of custody forms, processing logs, logbooks, and related documentation.
- Assist with deviation and investigation activities as needed.
- Provide updates during daily and weekly meetings.
- Participate in Lean Lab and Operational Excellence initiatives.
- Follow all safety, quality, GMP, and regulatory requirements.
- Perform other duties as assigned.
Experience:
- Bachelor's degree; or
- Associate degree plus 2+ years of experience in Quality Control or biopharma laboratories in an FDA-regulated environment; or
- High school diploma plus 3+ years of experience in Quality Control or biopharma laboratories in an FDA-regulated environment.
- Strong understanding of GMP in a QC laboratory setting.
- Excellent attention to detail and ability to manage multiple priorities.
- Proficiency with Microsoft Office, Excel, Visio, and related applications.
- Strong interpersonal, verbal, and written communication skills.
- Ability to work in a fast-paced, small-company environment and adjust to changing priorities.
- Flexibility to work overtime as needed.
- Sample management or QC lab support experience.
- Experience in a biopharmaceutical, pharmaceutical, or FDA-regulated laboratory.
- Familiarity with LIMS and sample tracking/documentation.
- Understanding of chain of custody and laboratory records.
- Strong organizational and communication skills.
- Cross-functional collaboration experience in a regulated environment.
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