Post Market Surveillance Specialist

Why Merit?

At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop 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

Maintains and implements process improvements for the Field Assurance Team. Assists with other post market surveillance activities as required.

Applicants must be based in our South Jordan, UT location and able to work on‑site.

ESSENTIAL FUNCTIONS PERFORMED

1.    

Performs complaint investigations and determines root cause. 

2.    

Reviews complaints to ensure compliance and accuracy.

3.    

Interacts with various levels of management, international regulatory affairs/quality assurance, and global regulatory bodies on the adverse event reporting process.

4.    

Maintains and implements improvement projects and provides training when needed.

5.    

Maintains appropriate records for the Global Quality Assurance adverse event reporting system as defined in relevant procedures. 

6.    

Prepares for, participates in and assists with FDA facility inspections, Notified Body Audits, Post Market Surveillance activities and other governmental inspections as directed.

7.    

Performs other duties and tasks, as needed.         

ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS 

    Lifting -- Not to exceed 50 lbs. – local practice may apply.Writing

    SittingStanding

    BendingVisual acuity

    Color perceptionDepth perception

    ReadingField of vision/peripheral

SUMMARY OF MINIMUM QUALIFICATIONS

    Education and/or experience equivalent to a Bachelor’s Degree and three years of related experience in a Quality/Regulatory related field.Knowledge of U.S. FDA regulations (21 CFR 803), the Medical Devices Directive (93/42/EEC, as amended), the European Medical Device Regulation 2017/745 (MDR), ISO 13485 Quality System Standards, and Canadian Medical Device Regulations.

    Experience with medical device global adverse event reporting required, such as MDR, MPR, and Vigilance, TGA, etc.Self-motivated, self-directing, strong attention to detail and excellent time management skills.

    Strong interpersonal skills and the ability to communicate well – verbally and in writing – with others.Project management experience.

    Demonstrated computer skills preferably spreadsheets, word processing, database, internet research and other applicable software programs.

PREFERRED QUALIFICATIONS

American Society for Quality (ASQ) Certifications - Certified Quality Auditor (CQA) 

    Regulatory Affairs Certification – RAC (Global).Experience with electronic submissions.

COMPETENCIES

    Global medical device adverse event reporting, such as MDR, MPR, TGA, and VigilanceComputer skills/internet research

    Interpersonal/communication skillsQuality system development/training    

COMMENTS

Infectious Control Risk Category II:

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 II states employment and procedures that may require exposure.

As an eligible Merit employee, you can expect the following:

* Multiple Shifts and Hours to choose from: Days, Swing (Eve), 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.