Quality Control Lab Support Technician I – Onsite, 4/10

Spectraforce Technologies, Inc.; Frederick (MD); On-site; USD 25,000 - 39,000; Full time

Job summary

Spectraforce Technologies, Inc. is hiring a Quality Control Technician I for the Frederick, MD lab, onsite for a 12‑month assignment. The role centers on sample management, logging in LIMS, shipping, and routine QC support in a GMP environment.

You’ll collaborate with QA, MM, and Corporate QC, handle documentation, and adhere to safety and regulatory guidelines while supporting continuous improvement initiatives in a fast-paced biotech setting.

Qualifications

• Bachelor's Degree or AA with 2+ years QC/biopharma lab experience
• High School Degree with 3+ years QC/biopharma lab experience
• FDA-regulated lab experience preferred

Responsibilities

• Receive incoming samples, verify documentation, and log sample information into LIMS
• Process sample receipt and preparation for release/stability testing
• Label, store, and organize samples per procedures and storage requirements
• Coordinate sample transfers to internal and external labs
• Perform routine cleaning, maintenance, and restocking of sample storage areas
• Collaborate with MM, QA, and other QC functions including Corporate QC
• Manage and complete all shipping activities within QC
• Review records like chain of custody, processing logs, and QC docs
• Assist with deviation and investigation activities as needed
• Provide updates during daily/weekly meetings
• Participate in Lean Lab and Operational Excellence initiatives
• Comply with safety, quality, and regulatory guidelines
• Perform other duties as assigned

Skills

GMP in QC lab

Attention to detail

Cross-functional collaboration

Interpersonal skills

Laboratory ELT/QA interaction

Education

Bachelor's Degree

AA Degree + 2+ years QC experience

High School Degree + 3+ years QC experience

Tools

Microsoft Office

Excel

Visio

Job description

Spectraforce Technologies, Inc. is hiring a Quality Control Technician I for the Frederick, MD lab, onsite for a 12‑month assignment. The role centers on sample management, logging in LIMS, shipping, and routine QC support in a GMP environment.

You’ll collaborate with QA, MM, and Corporate QC, handle documentation, and adhere to safety and regulatory guidelines while supporting continuous improvement initiatives in a fast-paced biotech setting.