- Locations: California, Texas, Florida, New York, Illinois
- Related Keywords: Complaints, Device, Medical Device Complaints, QA Medical Device Complaints
- Manufacturing Engineer
- MRINetwork (Philadelphia, PA)
- Great opportunity with a medical device company! Job Title: Complaint Specialist Salary up to 75K with bonus Overview:...summary addressing the alleged product complaint. Responsible for processing and closing complaints in a timely manner. Act as a CHU liaison with other...
- Manager, Regulatory Affairs
- BioTech Company (Boston, MA)
- ...Regulatory Affairs Manager position is for individuals with direct regulatory affairs experience for biotechnology-derived projects/products, primarily supporting complaints & adverse events and submission of clinical trial applications to regulatory agencies. This position acts as a...
- Global Complaints Manager - Medical Device Industry
- Human Captial Consultants (Braintree, MA)
- Global Complaints Manager Responsibilities: . Responsible for compliance of facilities to requirements...complaint compliance including: 1. PIR documentation, investigation & response 2. Device defects investigation and response 3. Services issues investigation and support...
- Senior Product Surveillance Analyst
- St. Jude Medical (Minnetonka, MN)
- ...seeking an electrophysiology (EP) Nurse for our Senior Product Surveillance Analyst. This Analyst will receive, review and investigate medical device complaints and maintain quality documents as required to ensure compliance with various regulatory agencies. Impact this role will have:...
- Clinical Research Manager
- Medtronic (Santa Rosa, CA)
- ...department to coordinate field staff and clinical site activities with study needs. Compile, review, and conclude device complaints . Provide management level representation during audits. Performs personnel related supervisory duties (eg, performance assessments, development of...
- Sr Clinical Research Spec
- Medtronic (Santa Rosa, CA)
- ...staff with all aspects of their responsibilities. . Supervise and review adverse event information. . Compile, review, and conclude device complaints . . Manage study closure activities. Additional Management Requirements . Strong knowledge of clinical research study design. . Working...
- Sr Clinical Research Spec
- Medtronic CardioVascular (Santa Rosa, CA)
- ...staff with all aspects of their responsibilities. * Supervise and review adverse event information. * Compile, review, and conclude device complaints . * Manage study closure activities. Additional Management Requirements: * Strong knowledge of clinical research study design. * Working...
- Principal CRS - Safety Management - CoreValve
- Medtronic (Minneapolis, MN)
- ...in follow-up and resolution of site issues noted by field and in-house Medtronicstaff. -Compile, review, and appropriately submit device complaints . -Assist data management group with review of clinical data/information and oversight of data correction. -Assist in preparation of...
- Clinical Research Manager
- Medtronic CardioVascular (Santa Rosa, CA)
- ...department to coordinate field staff and clinical site activities with study needs. Compile, review, and conclude device complaints . Provide management level representation during audits. Performs personnel related supervisory duties (eg, performance assessments, development of...
- Complaints Evaluator
- Unknown (Oakland, CA)
- ...cases.Candidate ProfileBe proficient with the complaint evaluation process and be able to review and assess customer complaints associated with medical device producs using software applications. Perform evaluation of complaints ensuring timely closure. Document evaluation clearly...
- Intern: MBA
- Medtronic (Santa Rosa, CA)
- ...with Clinical Operations department to coordinate field staff and clinical site activities with study needs. . Compile, review, and conclude device complaints . . Assist data management group with review of clinical data/information and provide oversight of data correction. . Work with...
- Sr Clinical Research Spec
- Medtronic (Minneapolis, MN)
- ...in follow-up and resolution of site issues noted by field and in-house Medtronic staff. -Compile, review, and appropriately submit device complaints (ie MDR reporting). -Assist data management group with review of clinical data/information and oversight of data correction. -Assist in...
- Senior Marketing Manager
- Medical Device Company (San Diego, CA)
- ...and reimbursement strategies, educating and training field sales, handling complaints , and supporting the global sales organization in meeting financial...AND EXPERIENCE: * 7+ years experience in a medical device company focused on vascular or structural heart disease *...
- Medical Device Manager - QM
- Business Services Company (Redmond, WA)
- ...FDA QSR, EU MDD, Canadian CMDR, and Australian TGA. Process complaints assigned to R&D for investigation per quality system regulations....in Engineering or Science 10+ years of experience with medical device regulatory and quality systems 10+ years of experience with...