Quality - Sample Management

Sample Management Associate This role is 100% Onsite at the Devens location Work Schedule: Monday - Friday, 2PM - 10PM Weekends are required as the business needs Responsibilities Perform routine processing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment. Executes routine procedures owned by the Sample Management functional area. Will work in teams and have continual interaction with members of his/her team as well as other sub-teams within QC and QSS, in order to exchange information regarding sample management as it relates to meeting department goals and objectives. Daily contact with her/his supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions. Preparing outgoing orders by QC testing labs Receiving incoming shipments of samples Data gathering for investigations Inventorying reference standards and critical reagents Experience Required Knowledge of basic electronic systems (email, MS Office, etc.) Knowledge of basic laboratory techniques such as working in a BSC, pipetting, aseptic technique; basic laboratory safety practices preferred. Familiarity with controlled temperature storage, sample inventory, and sample shipment and receipt. Attention to detail and demonstrated organizational skills. Demonstrated manual dexterity. Education requirements Highschool Diploma J-18808-Ljbffr