Quality Control Lab Support - Evening Shift (4/10)

Integrated Resources, Inc ( IRI ); Frederick (MD); On-site; USD 52,000 - 70,000; Full time

Job summary

Integrated Resources, Inc (IRI) is seeking a Quality Control Technician I for 100% onsite lab work in a fast-paced QC environment. The role supports sample management, testing, and disposition across QA, Analytical Development, Manufacturing, and Corporate QC teams.

The position requires a relevant degree with experience in a GMP/FDA-regulated setting, strong documentation practice, and capability to work swing shifts in a 3:00 PM–2:00 AM schedule.

Qualifications

• Bachelor’s Degree or AA with 2+ years in Quality Control or biopharmaceutical labs (FDA-regulated environment preferred).
• High School Diploma with 3+ years in Quality Control or biopharmaceutical labs (FDA-regulated environment preferred).

Responsibilities

• Receive and log incoming samples into LIMS; verify documentation.
• Process, aliquot, and prepare samples for release and stability testing.
• Label, store, and organize samples per procedures and storage requirements.
• Coordinate transfers to internal and external labs for testing.
• Maintain QC storage areas and perform routine cleaning and restocking.
• Support QC, QA, MM and Corporate QC teams with sampling, testing, and disposition.
• Manage QC-related shipping activities and review logs and records.
• Assist with deviation investigations as needed.
• Provide updates during daily/weekly meetings and participate in Lean Lab initiatives.

Skills

Attention to detail

Communication skills

Team collaboration

GMP awareness

Education

Bachelor’s Degree

Associate (AA) Degree

High School Diploma

Tools

Microsoft Office

Excel

Visio

Job description

Integrated Resources, Inc (IRI) is seeking a Quality Control Technician I for 100% onsite lab work in a fast-paced QC environment. The role supports sample management, testing, and disposition across QA, Analytical Development, Manufacturing, and Corporate QC teams.

The position requires a relevant degree with experience in a GMP/FDA-regulated setting, strong documentation practice, and capability to work swing shifts in a 3:00 PM–2:00 AM schedule.