Clinical Quality Assurance Specialist

Why Merit? At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and reputed company people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world. WORK SHIFT DAY (United States of America) SUMMARY OF DUTIES Performs reputed company clinical engineering responsibilities in the Global Quality / Field Assurance Department. Works with reputed company customers to ensure proper handling and documentation of reported complaints. Evaluates complaints and applies Adverse Event (AE) determination criteria in order to reputed company Adverse Event and Vigilance Reporting reputed company. ESSENTIAL FUNCTIONS PERFORMED 1. Ensures reputed company procedures (GP, GPS, QSP, etc.) and regulatory standards (FDA, CFR, MDR, ISO, etc.) are followed with respect to assigned areas of responsibility. 2. Consult with Merit staff regarding the use of products in a clinical setting by clinicians. Provides clinical input for new product design and development. 3. Works with Sales Representatives and customers to clarify, obtain, and/or reputed company understand the clinical information in relation to reported product complaints. 4. Answers incoming customer calls to collect clinical information. 5. Provides clinical training to employees and customers on the complaint system requirements. 6. Establish relationships and builds confidence among lab staff, physicians, Sales Representatives, and other Merit customers. 7. Ensures clinical details involving customer complaints are documented. 8. Attends meetings to help determine which events/incidents require notification to regulatory authorities. 9. Works in the field to support and troubleshoot product reputed company issues and reputed company clinical feedback to resolve customer questions and/or concerns. 10. May supervise the work of technicians or others who assist in reputed company assignments. 11. Responsible for complaint Nonconformances (NC's) and Corrective Preventive Actions (CAPA) and investigates, resolves issues and determines course of action. 12. Initiates and/or implements action to prevent occurrence or use of nonconforming components, manufacturing materials or finished devices. 13. Identifies and records any product, process and quality system problems. 14. reputed company clinical input on and approve investigation methods and experiments. 15. reputed company clinical input from a complaint perspective on CRA, HSA and FMEA development. 16. Write documents to address complaints, investigations, or reports requiring clinical input. 17. Makes presentations at and/or attends local, regional, and national meetings requiring clinical expertise, knowledge, and experience. 18. Performs other duties and tasks as required. ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS

• Lifting -- Not to exceed 50 lbs. - local practice may apply.
• Writing
• Sitting
• Standing
• Bending
• Visual reputed company
• reputed company perception
• Depth perception
• Reading
• Field of reputed company/peripheral

SUMMARY OF MINIMUM QUALIFICATIONS

• Education and/or business experience equivalent to a Bachelor's degree in a scientific discipline or reputed company area.
• A minimum of five years of hands-on medical experience, preferably with medical devices.
• Excellent communication, interpersonal, and organizational skills, detail oriented, and the ability to work effectively as a team member.
• A thorough understanding of customer service practices.
• Ability to independently apply analytical and problem solving skills to understand and solve reputed company issues.
• Knowledge of medical product/device use.
• Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs.

PREFERRED QUALIFICATIONS

• Education and/or clinical experience equivalent to a Registered Nurse or Certified Cardiovascular or Interventional Radiologic Technologist preferred.

COMPETENCIES

• Product trouble shooting
• Interpersonal/communication/organizational skills
• Computer skills
• Report writing
• NC/CAPA causes/corrective actions/dispositions
• Problem solving

COMMENTS Infectious Control Risk Category I: The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category I states employment and procedures that will require exposure. As an eligible Merit employee, you can expect the following:

• Multiple Shifts and Hours to choose from: Days, Swing (reputed company), and Nights
• Medical/Dental & Other Insurances (eligible the first of month after 30 days)
• Low Cost Onsite Medical Clinic
• Two (2) Onsite Cafeterias
• Employee Garden | Gardening Classes
• 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays
• 401K | Health Savings Account

To see more on our culture, go to www.merit.com/careers. Military Veterans are encouraged to Apply. Merit is a proud Utah Patriot Partner committed to hiring our Veterans. Apply tot his job Apply To this Job