Experience in Quality Systems (Veeva or Track Wise).
Day to Day Responsibilities:
General Quality Assurance activities related to support of the Quality Risk Management Global Process Owner; including maintaining metrics and documentation, providing guidance, interruption of GMP procedures.
General support of all QRM activities to ensure compliance throughout the network.
Must have the ability to interpret and apply Good Manufacturing Practices (GMP); quality assurance or manufacturing experience in the pharmaceutical or medical device industry and knowledge of Quality Risk Management principles applied in a pharmaceutical/drug/device/combo product environment.
Red Flags:
Candidates that have no quality experience
No Bachelors
No PHD
PAY RATE : $37-$43/hr on W2
"This posting is for Contingent Worker, not an FTE"