Job Title – Quality Control Technician I (QC Lab Support)
Work Arrangement: Fredrick, MD 21704, 100% Onsite (Laboratory Environment)
Shift & Schedule:

• Day Shift: 4 days × 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.

  
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 31.67/hr.