Quality Control Technician Jobs in USA, MD, Frederick | Rose International Job

Education:

• High School Required Skills:

• 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 Skills:

• 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

Summary:

• 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.
• Perform other duties as assigned.
• Only those lawfully authorized to work in the designated country associated with the position will be considered.
• Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.