- Medtronic (Lafayette, CO)
- …in a more connected, compassionate world. **A Day in the Life** As a Sr. MDR / Vigilance Specialist you will help to ensure Medtronic's mission to improve ... You will be responsible for the intake, documentation, Medical Device Reporting ( MDR ), and investigation of complaints for Surgical products. You will be required… more
- Abbott (Alameda, CA)
- …Group to gather appropriate information to determine whether a complaint requires an MDR and/or Vigilance report. Work with Complaint Investigation Group to ... 114,000 colleagues serve people in more than 160 countries. Specialist II Medical Events **Working at Abbott** At Abbott,...from a returned device investigation for submission of an MDR / Vigilance follow up report. Perform verification of… more
- Envista Holdings Corporation (Pomona, CA)
- …liaison with Ormco Regulatory Affairs as it relates to new product, MDR / vigilance reporting, product licensing/registrations and other regulatory or compliance ... This involves assuring quality standards (FDA, ISO, CMDCAS, MDD, MDR , MDSAP and Canadian Medical Device requirements) are with...FDA QSR (GMP), FDA OTC, ISO 13485, MDD, CMDCAS, MDR , MDSAP and Canadian Medical Device and other regulatory… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …@Olympus.com, it is likely not legitimate._ **Job Description** As a Medical Safety Specialist II (MSSII) you will have an integral role in the day-to-day ... detection. + Demonstrates knowledge and experience working with various regulations (HIPPA, EU- MDR , FDA 21 CFR Part 803, 806, 820), various standards (GCP, ISO… more
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