Quality Control Technician
Listed on 2026-08-10
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Production QC/QA
Quality Control Technician I
Location:
Frederick, MD Swing
Shifts:
4/10 (4 days x 10 hours/day) Wed - Sat. 3:00-PM
-2:00-AM (2 openings) Contract Duration: 12 Months Pay Range: $18.00 - $21.58 USD hourly on W2
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.
Responsibilities (include but are not limited to):- 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 OR
· 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 communications 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
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