Medtronic

Associate Regulatory Affairs Specialist

Medtronic

Minneapolis, MN, USA
Full-TimeDepends on ExperienceMid-LevelBachelors
Job Description

As an Associate Regulatory Affairs Specialist at Medtronic, you will be part of a dynamic and dedicated team responsible for the regulatory compliance of our products. We are looking for a highly organized and detail-oriented individual to support the regulatory team in achieving our goals. The ideal candidate for this position will have excellent communication and problem-solving skills, as well as a strong understanding of the regulatory processes. To be successful in this role, you will need a Bachelor’s degree in a related field, a minimum of two years of regulatory experience in the medical device industry, and an understanding of the regulatory requirements in the countries we operate in. If you have a passion for compliance and are ready to take on the challenge of ensuring our products meet the highest standards, we want to hear from you!

Responsibilities:

  1. Ensure our products are compliant with regulatory requirements in the countries they are sold in.
  2. Maintain up-to-date knowledge of regulatory changes in the medical device industry.
  3. Develop and implement strategies to stay in compliance with international regulations.
  4. Work closely with the regulatory team to ensure timely filing of applications and submissions.
  5. Monitor the progress of regulatory submissions and follow up on any questions or concerns.
  6. Prepare reports and summaries for regulatory reviews.
  7. Investigate and troubleshoot any regulatory-related problems.
  8. Act as a liaison between Medtronic and regulatory bodies.
  9. Provide guidance and support to other members of the team.
  10. Develop and maintain strong relationships with external partners.
Where is this job?
This job is located at Minneapolis, MN, USA
Job Qualifications
  • Analytical And Problem Solving Skills

  • Proficiency In Microsoft Office Suite

  • Good Communication And Organizational Skills

  • Strong Scientific Background

  • Knowledge Of Relevant Regulations/Guidelines

  • Ability To Multitask And Prioritize Work

  • Ability To Work Independently And In A Team

  • Knowledge Of Medical Device Product Development

Required Skills
  • Documentation

  • Quality Assurance

  • Process Improvement

  • Project Management

  • Data Analysis

  • Communication

  • Negotiation

  • Auditing

  • Tracking

  • Technical Writing

  • Reporting

  • Compliance

  • Product review

  • Risk assessment

  • Regulatory

Soft Skills
  • Communication

  • Emotional Intelligence

  • Problem Solving

  • Time management

  • Interpersonal Skills

  • creativity

  • Organization

  • flexibility

  • Critical thinking

  • Teamwork

Compensation

According to JobzMall, the average salary range for a Associate Regulatory Affairs Specialist in Minneapolis, MN, USA is $55,000 to $90,000 annually. This salary range is an estimate and will vary depending on the individual's experience, qualifications, and employer.

Additional Information
Medtronic is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedSeptember 26th, 2023
Apply BeforeMay 22nd, 2025
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About Medtronic

Medtronic plc is the world's largest medical device company that generates the majority of its sales and profits from the US healthcare system and is headquartered on the island of Ireland.

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