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Quality Control Laboratory Technician

ACL Digital

Job Description

Job Title: Quality Control Technician I - QC Lab Support

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Duration: 12+ months

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Location: Frederick, MD

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Pay Rate: $22/hr on w2

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100% onsite (lab environment)

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Swing Shifts: 4/10 (4 days x 10 hours/day)

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Wed - Sat. 3:00pm - 2:00am

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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.

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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.

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· Perform other duties as assigned.

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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

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· High School Degree and 3+ years’ experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory.

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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

Vacancy posted 22 days ago
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