Our client, a leading pharmaceutical company, is hiring a Sample Management consultant on a contract basis.
Work Location
Devens, MA/Onsite
Summary:
Sample Management Associate
This role is 100% Onsite
Work Schedule: Monday – Friday, 2PM – 10PM
*Weekends and holidays are required as the business needs*
Responsibilities:
1. 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.
2. Executes routine procedures owned by the Sample Management functional area.
3. 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.
4. Daily contact with her/his supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions.
5. Preparing outgoing orders by QC testing labs
6. Receiving incoming shipments of samples
7. Data gathering for investigations
8. Inventorying reference standards and critical reagents
Experience Required:
1. Knowledge of basic electronic systems (email, MS Office, etc.)
2. Knowledge of basic laboratory techniques such as working in a BSC, pipetting, aseptic technique; basic laboratory safety practices preferred.
3. Familiarity with controlled temperature storage, sample inventory, and sample shipment and receipt.
4. Attention to detail and demonstrated organizational skills.
5. Demonstrated manual dexterity.
Education requirements:
High school Diploma