NEW JOB OPENING
LAB TECH
IN Frederick, MD, USA!

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



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.

• **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.**