Clinical Product Surveillance Specialist

Job Summary JOB SUMMARY : Under general supervision, use knowledge of clinical workflow and product use in assessing incoming complaints and hazards. Assist in post-market reportability determination. Participate in clinical investigations for reported product incidents and submit adverse event reports. Provide clinical resource support to customers, sales reps and the product division for clinical issues. Identify hazardous situations from product design, product / material assessments, and customer complaints.Job Description MAJOR RESPONSIBILITIES : Identify and evaluate complaints which affect patient safety. Prepare and submit Medical Device Reports (MDRs) to the FDA. Process MDRs and coordinate international report filing with local health authorities. Ensure reportable complaints are processed and submitted. Collaborate with team members; act as a clinical resource to QA and product division. Review, evaluate and classify potential reportable customer safety complaints. Ensure customer communications are created and issued; review customer responses for technical accuracy related to Medline products. Conduct risk analysis and design development modifications for new and existing products; provide clinical insight, review, and risk controls leads. Analyze patient safety and risk data. Ensure compliance with applicable post-market regulations. Identify product safety issues; triage complaints for further investigation. Maintain procedures for MDR / Adverse Event Reporting for medical device, drug, FDA regulated products and international products. Assess HHE product recalls. Conduct trainings related to post-market surveillance, clinical use, product risk, and SOP requirements. Education & Work Experience - Bachelor's degree in medical science, health sciences or healthcare related field and at least 2 years of clinical, medical device risk management, or pharmaceutical risk management experience OR Healthcare provider certificate / licensure. Knowledge / Skills / Abilities - Demonstrated ability to analyze and report data in order to identify issues, trends, or exceptions to drive improvement of results and find solutions. - Communication skills to convey technical information to non-technical audiences. - Skills and ability to work with cross-functional teams and facilitate teams to identify and implement solutions to complex problems. - Time management skills such as prioritizing / organizing and tracking details and meeting deadlines of multiple projects with varying completion dates. - Ability to accomplish goals with little or no supervision, depending on oneself to complete objectives and determining when escalation of issues is necessary. PREFERRED JOB REQUIREMENTS - Bachelor’s Degree in Nursing. - Licensed, registered, or certified by a state or other governing body to administer health care. - Experience applying knowledge of FDA and international Health Authority reporting requirements. - Understanding of the clinical environment and product work flow. - Familiarity with the application of medical device as it relates to patient safety. Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization. The anticipated salary range for this position : $79,560.00 - $115,440.00 AnnualThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and / or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold. Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here . For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here . Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.