Quality & Regulatory Affairs (QA/RA)

Quality Assurance Regulatory Affairs is responsible for ensuring our products and services are safe and effective and that Olympus follows all regulations in the countries where our products are sold.

Quality Assurance Regulatory Affairs is responsible for ensuring our products and services are safe and effective and that Olympus follows all regulations in the countries where our products are sold.

 

 

QA/RA supports Patient Focus by ensuring our products remain safe, effective, and follow the regulations in the regions in which we operate.    

QA/RA supports Patient Focus by ensuring our products remain safe, effective, and follow the regulations in the regions in which we operate.

Req ID Title Sort descending Location
9905 Global MDR Submissions Analyst III
9905 Global MDR Submissions Analyst III Center Valley, PA, US, 18034-0610
Center Valley, PA, US, 18034-0610
9906 Global MDR Submissions Analyst III
9906 Global MDR Submissions Analyst III Center Valley, PA, US, 18034-0610
Center Valley, PA, US, 18034-0610
9599 Global MDR Submission Analyst III
9599 Global MDR Submission Analyst III Center Valley, PA, US, 18034-0610
Center Valley, PA, US, 18034-0610
9962 Clinical Evaluation Report Manager
9962 Clinical Evaluation Report Manager Center Valley, PA, US, 18034-0610
Center Valley, PA, US, 18034-0610
9992 Analyst II, Global MDR Submissions
9992 Analyst II, Global MDR Submissions Westborough, MA, US, 01581
Westborough, MA, US, 01581
9650 Analista de Tecnovigilância II
9650 Analista de Tecnovigilância II Sao Paulo, SP, BR, 04552-906
Sao Paulo, SP, BR, 04552-906