Archiving of data in the RIMS system

Performs Routine Review of Lab test data including On-the-Floor Review, and Off-the-Floor Review for low complexity test methods.

Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements

Understand, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements

Accepts responsibility to complete assigned tasks as committed. Works with other to maintain a positive atmosphere to accomplish business objectives

Supports the review team with administrative tasks such as logbook management and scanning/filing of data.

Participates in training of other employees, but focused on demonstration and not management of training delivery

Bachelor’s Degree OR High School Diploma with 3-5 + years of combined experience in manufacturing, QA, QC in pharmaceutical or biologics industry