). SAP Quality Module (plus skill). Experience working in a medical devices or life sciences space. Experience with ISO... 13485 (specific to life sciences/med devices industry)....
Responsibilities: Demonstrated practical understanding of SAS programming concepts and techniques appropriate to the pharmaceutical industry. Demonstrated satisfactory ability to apply SAS programming knowledge and work independently to ...
Responsibilities: Process and equipment qualification (IQ/OQ/PQ). Development of test methods for Design V&V, Process Validation, and Production. Validation of test methods. Execution of Engineering Builds, Gauge R&R Studies, Attrib...
Responsibilities: Initiate, update, and optimally close all product safety, medical device/IVD complaints. Lead all CAPA program activities including taking ownership of CAPA program and driving changes where appropriate. Establish an...