Tech Ops and Quality - Quality Assurance Associate I
LanceSoft - Chicopee, Massachusetts, us, 01021
Work at LanceSoft
Overview
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Overview
Job Title: Quality Control Technician I - QC Lab Support 100% onsite (lab environment) Pay Rate: $28.00/hr 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)
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): • 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 • 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.