This individual will ensure that the stability group functions smoothly in support of the Lifecore Stability Program by performing routine lab support activities including, but not limited to, initiating stability studies, monitoring stability chamber functions, pulling and logging in stability samples, and disposing of excess or completed samples. They will review documentation; monitor stability chambers, identify and report equipment failures, perform routine cleaning, and change settings as needed; receive, label, and initiate new stability studies based on the study schedule;pull and log into the laboratory; enter and QA stability data; dispose of lab samples; coordinate receipt and storage of all stability samples; filecompleted data sets; perform annual inventory audit.
Requirements: High school diploma with a minimum of 2 years of experience working in a GMP or GLP regulated environment (pharmaceutical or medical device preferred). Experience with quality control activities in a laboratory settingpreferred. Basic understanding of computer word processing and spreadsheet software; proven ability take work direction and independently complete tasks on time. Proven ability to maintain a high attention to detail while working in a fast-paced environment.
4 1/2 or 5 day work week, Monday - Friday
Job Posted by ApplicantPro