Duration: 12+ months
Available Shifts:
SUN-WED: 7:00am-6:00pm
WED-SAT: 7:00am-6:00pm
SUN-WED: 3:00pm-2:00am
WED-SAT: 3:00pm-2:00am
Overview:
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:
Basic Qualifications:
Preferred Qualifications:
Available Shifts:
SUN-WED: 7:00am-6:00pm
WED-SAT: 7:00am-6:00pm
SUN-WED: 3:00pm-2:00am
WED-SAT: 3:00pm-2:00am
Overview:
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:
- 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.
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