LanceSoft Inc
Job Title : Quality Control Technician I - QC Lab Support
Location : Frederick, MD
Contract Duration : 12 Months
Day Shifts : 4/10 (4 days x 10 hours/day)
Shift : Sunday - Wednesday. 7:00-AM - 6:00-PM
Pay Range : $28.00 - $31.00 USD hourly on W2
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
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Location : Frederick, MD
Contract Duration : 12 Months
Day Shifts : 4/10 (4 days x 10 hours/day)
Shift : Sunday - Wednesday. 7:00-AM - 6:00-PM
Pay Range : $28.00 - $31.00 USD hourly on W2
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
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