- Locations: California, Massachusetts, Pennsylvania, New Jersey, Illinois
- Related Keywords: Complaint, Device, Medical Device Complaint
- Project Manager, Clinical Studies
- Executive Recruiting Firm (NY)
- Clinical Project Manager, Medical Device Clinical Trials (Job ID 186 PJM) Collaborate with regulatory affairs,...Class III products. Using your medical education and training complete complaint investigations and manage safety data. Primary Responsibilities Manages adverse event...
- Regulatory Affairs Manager
- Medical Company (Boston, MA)
- ...program Review advertising and promotion materials, and those of competitors Manage the adverse event program, reviewing customer complaint investigation results; assessing and investigating potential adverse events and incident reports.. Manage recall and removal activities; assess...
- Group Director, Regulatory Affairs
- Global Medical Device Company (Memphis, TN)
- ...emerging regulations, standards, guidance, and best practices for medical devices; labeling and marketing material compliance and translations; device complaint handling, adverse event reporting, remedial action, and related regulatory reporting; directing and overseeing the work of...
- Healthcare Customer Service Representative II
- TMS Health (Boca Raton, FL)
- ...program changes, and specifications on assigned brands. 6. Identify and handle actual and potential non-serious Adverse Event (AE) reports and/or Device complaint . 7. Assess each reported AE/ Device Complaint as serious or non-serious per regulations. 8. Monitor consumer...
- QA Engineer
- Unknown (Aloha, OR)
- ...in Medical Device Industry.Project Description:Product Support and Complaint Handling Engineer/ SpecialistDaily Responsibilities:Support Medical Device Complaint handling processInitial evaluation of product issue reportsMaintain complaint filesCoordinate complaint ...
- Manager, Medical Devices Product Monitoring (St. Louis / Cincinnati)
- Tyco Healthcare (Hazelwood, MO)
- ...with external and internal customers. Essential Functions: 1. Responsible for the day to day functioning of PM relative to medical device product complaint handling and the providing of medical information for medical devices. 2. Ensure compliance of PM with corporate level procedures...
- Quality Assurance Engineer - Medical Devices
- Yoh (Bellevue, WA)
- ...procedures compliant to device quality system regulations and standards, and drug manufacturing regulations. Coordinate and track device complaint investigations Conduct internal and external (supplier) quality audits Travel up to 20% Other duties as assigned Contacts: Primary...
- Global Product Safety & Complaint Analyst
- Kelly Scientific Resources (Lake Forest, IL)
- ...call center experience with internal/external customers highly desired Must have demonstrated experience in drug safety/product complaint (drug or medical device ) environment for a pharmaceutical or biotech company Extremely professional with strong people skills, communication skills...
- Product Surveillance Technician
- ZIMMER (Warsaw, IN)
- ...JD Edwards, DCS, QC View, Livelink, Zimpack. - Must be able to navigate these systems to retrieve product specifications, inspection requirements, device history records, and complaint history records. - Excellent written and oral communication skills required, as the position requires...
- Clinical Research Monitor(CRA)
- Medtronic (Atlanta, GA)
- ...cath lab staff at clinical sites. . Participate in regular teleconferences, staff meetings, etc. . Assists with compilation of device complaint documentation. . Serves as liaison between Medtronic personnel and site personnel. Provides site feedback or input to appropriate departments....
- Clinical Research Monitor(CRA)
- Medtronic (Philadelphia, PA)
- ...cath lab staff at clinical sites. ? Participate in regular teleconferences, staff meetings, etc. ? Assists with compilation of device complaint documentation. ? Serves as liaison between Medtronic personnel and site personnel. Provides site feedback or input to appropriate departments....
- Clinical Research Monitor (CRA)
- Medtronic CardioVascular (Houston, TX)
- ...cath lab staff at clinical sites. * Participate in regular teleconferences, staff meetings, etc. * Assists with compilation of device complaint documentation. * Serves as liaison between Medtronic personnel and site personnel. Provides site feedback or input to appropriate departments....
- Product Surveillance Technician
- ZIMMER (Warsaw, IN)
- ...JD Edwards, DCS, QC View, Livelink, Zimpack. - Must be able to navigate these systems to retrieve product specifications, inspection requirements, device history records, and complaint history records. - Excellent written and oral communication skills required, as the position requires...
- QA Engineer
- Unknown (Aloha, OR)
- ...in Medical Device Industry.Project Description:Product Support and Complaint Handling Engineer/ SpecialistDaily Responsibilities:Support Medical Device Complaint handling processInitial evaluation of product issue reportsMaintain complaint filesCoordinate complaint ...