Post-Market Surveillance Consultant

Andover - Massachusetts - United States - Life Sciences & Health Care - Medical devices - Regulatory - Academic Master

We’re hiring a Post-Market Surveillance Consultant for our client, a global healthcare/medical device company, to join their team. This is a contract concluding in August 2020.

Feel free to contact

Maria Camanag, Account manager

Apply now

About this role

Responsibilities

  • Handle the receipt, processing, monitoring, and reporting of product defect complaints,
  • Make MDR determination, investigate document the all activities creating the summaries of the investigation.
  • Documented product complaints into the database for trending and analysis and ensured the complaint process was completed in accordance with corporate procedures, follow the complaint file all the way until completion.
  • Developing professional expertise, applies company policies and procedures to resolve a variety of issues.
  • Interfaces with Customer Service and customers/patients to gather additional information required for complaint initiation/investigations: including the retrieval of product samples and or durable equipment retrieval for evaluation.
  • Ensure that complaints from multiple sources are tracked.
  • Determines product and incident complaint codes based on the master symptom code severity list. Applies knowledge of device regulatory requirements in order to support the Post Market Clinical Surveillance reporting process
  • Evaluates complaints for reporting, partners with other departments to resolve product problems and provides feedback to customers as needed.
  • Assists with review of the timely coding of completed investigations, closure of all complaint files, and ensures that all pertinent information is contained consistently and uniformly within the file prior to closure.
  • Performs queries to provide complaint data and ad hoc trend analysis on reported product problems/complaints.
  • Reviews and complies with the all applicable company policies and procedures, local, state, and federal laws and regulations.
  • CAPA support in response to audit readiness findings and in preparation for audits.
  • Coordinate initiative to close out overdue Field Change Orders with global markets.
  • Provide team members with training on a variety of assignments.
  • Prepare presentations for weekly management/steering committee meetings.

About you

Requirements

  • 15 years professional experience in the applicable role.
  • Education: Bachelor's/Master's degree or equivalent.
  • Expert and technical lead with proven experience.

What we offer

Why work with Brunel? We are proud to offer exciting career opportunities from over 100 offices globally in 42 countries. Advancing your career takes time and effort – let us match you to your ideal position.

About us

Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 40 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.

Summary

  • Vacancy number: PUB254917
  • Location: Andover
  • Market: Life Sciences & Health Care
  • hours per week: 40
  • Branch: Medical devices
  • Education level: Academic Master
  • Area of Expertise: Regulatory
  • Closing date: Monday, April 6, 2020
Apply now

Feel free to contact

MC

Maria Camanag

Account manager Brunel Canada Toronto

+1 416 244 2402

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