Sr Associate Quality Complaints

Location: Thousand Oaks, CA
Date Posted: 06-08-2017
Day to Day Responsibilities:     
Coordinate external product complaint investigations. Interface with various Amgen sites and business partners to ensure process compliance. Complete and approve product complaints requiring further investigation. Reconcile reported product complaints to ensure entry in IRPC. Archive documents related to product complaints.

Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation and documentation according to company guidelines. Be self motivated, attentive to details and able to prioritize and meet deadlines. Basic statistical mathematical skills including the ability to trend data. Basic project management skills. Independently understand, follow and implement instructions. Strong word processing, database and spreadsheet application skills. Strong organizational skills with the ability to manage multiple projects or assignments.

"This posting is for Contingent Worker, not an FTE"
this job portal is powered by CATS