Job Title: Quality Control Technician I - QC Lab Support
Location
Frederick MD
Duration: 12 Months
Job Title: Quality Control Technician I - QC Lab Support
100% onsite (lab environment)
Swing Shifts: 4/10 (4 days x 10 hours/day)
Wed - Sat. 3:00pm-2:00am
Duration: ongoing temp
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)
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Receive incoming samples, verify documentation, and log sample information into LIMS.
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Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
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Label, store, and organize samples according to established procedures and storage requirements.
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Coordinate sample transfers to internal and external testing labs.
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Perform routine cleaning, maintenance, and restocking of sample storage areas.
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Collaborate with MM, QA, and other QC functions—including Corporate QC—to support requirements around sampling, testing, and disposition.
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Manage and complete all shipping activities within QC functions.
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Complete routine review of records, such as sample chain of custody forms, processing logs, logbooks, and other documentation generated within QC Lab Support.
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Assist with deviation and investigation activities as needed.
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Provide updates during daily and weekly meetings.
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Participate in Lean Lab and other Operational Excellence initiatives.
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Comply with all safety, quality, and regulatory guidelines.
· Perform other duties as assigned.
Basic Qualifications
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Bachelor’s Degree OR
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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
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Strong knowledge in applying GMP in QC lab.
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Exceptional attention to detail and ability to keep track of multiple ongoing projects
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Proficient in Microsoft Office, Excel, Visio, and other related applications
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Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment
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Comfortable in a fast-paces small company environment and able to adjust workload based on changing priorities.
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Ability to be flexible with schedule, and work overtime as needed
