Overview
Quality Control Sample Management Specialist Jobs in Frederick, MD at Integrated Resources, Inc ( IRI )
Title: Quality Control Sample Management Specialist
Company: Integrated Resources, Inc ( IRI )
Location: Frederick, MD
Role: 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.
Basic Qualifications:
· 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.
Preferred Qualifications:
· 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-paces small company environment and able to adjust workload based on changing priorities.
· Ability to be flexible with schedule, and work overtime as needed
Reports to: Manager, Quality Control Lab Support
The team will operate 7 days a week, with an extended, overlapping shift structure.
