Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have improved the lives of hundreds of thousands of patients by using innovative technology that is wearable, waterproof, and lifestyle accommodating.

We are looking for highly motivated, performance driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

Position Overview

Review, analyze, and compose responses to regulatory agencies regarding medical device reportable events and collaborate both within post market surveillance and across other functions, including customer care, quality, clinical and regulatory to help ensure compliance with reporting requirements and good documentation practices.

This position reports to the Director EMEA Vigilance and QARA

Responsibilities

Act as the local vigilance contact with the Spanish competent authority

Act as the representative for the regions under their responsibility

Support activities for global vigilance reporting such as

Process, prepare, write and submit RFAI requests from Competent Authorities

Maintain the Vigilance Mailbox and monitor emails

Support cases reportability assessment when needed by completing due diligence on additional information requests with the complaint reporter

Critically interpret results of trending reports, failure investigations/engineering reports and determines how to present the data most effectively in a succinct manner.

Attend/support meetings with the competent authorities

Liaise with external partners (ex. Distributors) regarding vigilance and quality matters

Process due diligence requests

Process investigation results requests

Collaborate with other functions to compile compliance documentation for post market.

Follow processes and operational policies in selecting methods and techniques for obtaining solutions.

Support regional markets with activities related to product being introduced or currently on the market

Provide support as needed for internal and external audits/inspections

Complete administrative verification on product to be distributed on the EU markets as needed

Act as local Regulatory point of contact in Spain

Complete regulatory review and validation of material intended for use with third parties in Spain

Education And Experience

Minimum Requirements:

Relevant experience in professional writing in a medical technology, life sciences, or healthcare setting

Complaint processing experience

Knowledge of the EU MDR 745/2017 and country specific vigilance related regulations,

BA/BS degree

Effective verbal and technical writing skills. Ability to communicate at multiple levels of an organization.

Ability to organize and judge priorities.

Ability to assimilate and interpret scientific content, and translate information for appropriate audience in a succinct manner

Strong attention to detail with excellent grammatical, editorial, and proofreading skills

Spanish native speaking person, must be fluent in speaking and writing in English

Preferred Skills And Competencies

Willingness to pursue additional learning and build qualifications in professional field, as required.

Experience leading/managing improvement projects.