Job Title - Quality Control Technician I (QC Lab Support)
Work Arrangement: Fredrick, MD 21704, 100% Onsite (Laboratory Environment)
Shift & Schedule:
- Day Shift: 4 days O 10 hours
- Sunday - Wednesday | 7:00 AM - 6:00 PM
Duration: 12 Months
Role Overview
The Quality Control Technician I - QC Lab Support is responsible for executing activities related to
sample management, sample shipment, and laboratory support within the QC function. This role requires close cross-functional collaboration with
Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), Corporate QC, and other QC teams to ensure compliant and efficient laboratory operations.
Key Responsibilities
- Receive incoming samples, verify documentation, and log sample information into LIMS.
- Support sample receipt, processing, and aliquoting for release, stability testing, and retain samples.
- Label, store, organize, and maintain samples according to established procedures and storage requirements.
- Coordinate sample transfers to internal and external testing laboratories.
- Perform routine cleaning, maintenance, and restocking of sample storage areas.
- Collaborate with MM, QA, and QC functions, including Corporate QC, to support sampling, testing, and disposition activities.
- Manage and complete shipping activities within QC functions.
- Review and complete documentation, including chain-of-custody forms, processing logs, logbooks, and other QC records.
- Assist with deviations and investigations as needed.
- Provide updates during daily and weekly meetings.
- Participate in Lean Lab and other Operational Excellence initiatives.
- Ensure compliance with all safety, quality, and regulatory guidelines.
- Perform additional duties as assigned.
Basic Qualifications
- Bachelor's Degree, OR
- Associate's Degree with 2+ years of experience in Quality Control or biopharma laboratories (FDA-regulated preferred), OR
- High School Diploma with 3+ years of experience in Quality Control or biopharma laboratories (FDA-regulated preferred).
Preferred Qualifications
- Strong knowledge of GMP application in a QC laboratory environment.
- Exceptional attention to detail and ability to manage multiple priorities.
- Proficiency in Microsoft Office, Excel, Visio, and related applications.
- Excellent interpersonal, verbal, and written communication skills in a collaborative environment.
- Comfortable working in a fast-paced, small company environment with shifting priorities.
- Flexible with schedule and willing to work overtime as needed.
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Spectraforce Technologies
Jan 10, 2026