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Job Title: Quality Control Technician I - QC Lab Support (Sample Management/ LIMS)
100% onsite (lab environment)
SWING Shifts: 4/10 (4 days x 10 hours/day)
SUN-WEDS 3:00pm-2:00am (1 opening)
WEDS-SAT 3:00pm-2:00am (1 opening)
DAY Shifts: 4/10 (4 days x 10 hours/day)
SUN-WEDS 7:00am-6:00pm (1 opening)
WEDS-SAT 7:00am-6:00pm (1 opening)
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.
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