Hiring.Camp

Senior Regulatory Affairs Specialist

Medtronic

·

Today

Location
CHE-VD Tolochenaz Molliau, Switzerland
Workplace
Onsite
Type
Full-time
Department
Legal
Seniority
Senior
Experience
4+ years
Education
Bachelor
Source
Workday

Description

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life


Responsibilities may include the following and other duties may be assigned.

  • Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and inspections.
  • Leads or compiles all materials required in submissions, license renewal and annual registrations.
  • Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance.
  • Monitors and improves tracking / control systems.
  • Keeps abreast of regulatory procedures and changes.
  • May direct interaction with regulatory agencies on defined matters.
  • Recommends strategies for earliest possible approvals of clinical trials applications.

Required Knowledge and Experience: 


  • Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, Regulatory Affairs, Quality, Clinical, or a related technical discipline.
  • 4+ years of professional experience with a bachelor's degree, or 2+ years with an advanced degree.
  • Experience working in a regulated environment (medical device, pharmaceutical, biotechnology, healthcare, manufacturing, clinical, or similar).
  • Experience interpreting technical information, assessing risks, and making recommendations.
  • Demonstrated ability to work independently and manage multiple priorities.
  • Strong written and verbal communication skills.
  • Experience collaborating with cross-functional teams and influencing stakeholders

#LI-Onsite

 

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

 

 

Recruitment Fraud Alert 

We are aware of phishing scams targeting job seekers. Please keep the following in mind: 


Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. 


Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. 


If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. 


If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected]

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
 

 

Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik:  Switzerland: 115,200.00 CHF - 172,800.00 CHF | 

 

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

Skills

Clinical TrialsCompliance

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Senior Regulatory Affairs Specialist at Medtronic | Hiring.Camp