QC Technician I

Position: QC Technician ILocation: Frederick, MD 21704Duration: 12 MonthsJob Type: Temporary Assignment Work Type: OnsiteSun - Wed. 7:00 am-6:00 pmDAY Shifts: 4/10 (4 days x 10 hours/day)Pay Rate: $ 19.00-21.00/hr.Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.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 ORAA Degree and 2+ years’ experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory ORHigh 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 projectsProficient in Microsoft Office, Excel, Visio, and other related applicationsExcellent interpersonal, verbal and written communications skills which are essential in this collaborative work environmentComfortable 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 neededReports to: Manager, Quality Control Lab SupportThe team will operate 7 days a week, with an extended, overlapping shift structure.TekWissen® Group is an equal opportunity employer supporting workforce diversity.