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:

High school Diploma