Supports multiple banner ads per page, from any ad serving software. Flexible banner sizes
1+ months

Principal Regulatory Affairs Specialist

Mounds View, MN 55112
Apply Now
Applying for this job will take you to an external site
Principal Regulatory Affairs Specialist


Mounds View, Minnesota, United States

Requisition #:


Post Date:

Mar 16, 2021


Join a diverse team of innovators who bring their worldview, their unique backgrounds, and their individual life experiences to work every day. Its no accident we work hard to cultivate a workforce that reflects our patients and partners. We believe its the only way to drive healthcare forward and remain a global leader in medical technology and solutions

**_Careers that Change Lives_**

The **PrincipalRegulatory Affairs Specialis** t is responsible for developing regulatory strategies, preparing U.S. and international submissions and obtaining and maintaining approval for products and therapies to markets worldwide.Additionally, the Principal Regulatory Affairs Specialist is responsible for assessment of device changes for regulatory implications and for performing regulatory activities in support of implementing these device changes.

**Preferred Location: Mounds View, MN; Open for Remote**

**A Day in the Life / Responsibilities:**

+ Define the regulatory strategy and manage regulatory submission activities for complex product development activities and product maintenance for existing approved products.

+ Team with business unit Regulatory Affairs Specialists (RAS) and international regulatory staffs to provide regulatory support for new products/therapies and changes to existing products. Work with RAS, engineers and technical experts to resolve potential regulatory issues and questions from regulatory agencies.

+ Prepare regulatory (e.g., FDA/Notified Body) submissions for new products and product changes, as required, to ensure timely approvals for clinical studies and market release. Review significant product submissions with manager and negotiate submission issues with agency personnel.

+ Provide support to currently marketed products as necessary. This includes reviewing labeling, promotional material, product changes and documentation for changes requiring government approval.

+ Interact directly with FDA/Notified Body and indirectly with international regulatory agencies on most projects/products at reviewer level. All significant issues will be reviewed with the manager.

+ Support regulatory compliance activities, including manufacturing site registration, audits, etc., as needed.

+ Maintain proficiency in worldwide regulatory requirements; establish and maintain good relationships with agency personnel.

+ Provide business and product information to international regulatory staffs to enable development of strategies and requirements and communicate that information to business teams.

+ Provide feedback and on-going support to product development teams for regulatory issues and questions.

+ Ensure personal understanding of all quality policy/system items that are personally applicable.

+ Follow all work/quality procedures to ensure quality system compliance and high-quality work.

**Must Have (Minimum Requirements):**

+ Bachelors degree required with a minimum of 7years of experience in regulatory affairs in the medical device industry,or advanced degree with a minimum of 5years of experience in regulatory affairs in the medical device industry.

**Nice to Have (Preferred Qualifications):**

+ Advanced degree in a scientific discipline (engineering, physical/biological or health sciences).

+ Experiencewith 510(k)/IDE/PMA device product submissions and other worldwide submissions and clearances.

+ Experience performing advertising and promotion reviews for medical devices.

+ Experience with FDA and international regulatory agency requirements

+ Effective interpersonal skills.

+ Effective team member.

+ Ability to comprehend principles of engineering, physiology and medical device use. Good analytical thinking skills.

+ Ability to effectively manage multiple projects and priorities.

+ Proficient computer skills.

+ Project management skills.

+ Excellent oral and written skills.

+ Excellent analytical thinking skills.

**About Medtronic**

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.

Physical Job Requirements

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


Posted: 2020-12-24 Expires: 2021-04-25
Supports multiple banner ads per page, from any ad serving software. Flexible banner sizes

Job Rated Report

Resume Writing Advice

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Principal Regulatory Affairs Specialist

Mounds View, MN 55112

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast