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Job Title:  Regulatory Affairs Intern

Req ID:  29750
Job Category:  Regulatory Affairs

Eden Prairie, MN, US, 55344


At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

Position Summary

The Regulatory Affairs Intern will be responsible for supporting the Key Surgical/STERIS Regulatory Manager by reviewing and preparing international regulatory documentation, in preparation for changing regulatory requirements in the United Kingdom. The Intern is responsible for keeping abreast of and providing regular reporting the Key Surgical/STERIS Regulatory Manager regarding important regulatory developments that impact customers, compliance, or to Key Surgical/STERIS’s business directly. 

What you will do

  • Identify regulatory requirements for legacy Key Surgical/STERIS products in preparation for the MHRA - UK Conformant Assessment (UKCA).
  • Gather and compile technical documentation and supporting information to complete the UKCA audit and application.
  • Use this information to prepare Technical Documentation and necessary submission material in a complete and thorough format for Key Surgical/STERIS product families.
  • Work cross-functionally with Key Surgical teams to lead the UKCA Project.

Education Degree

  • Bachelor's Degree

What you need to be successful

  • Candidates must have a Bachelor's degree or be actively seeking completion of a Bachelor's degree
  • Previous medical device education or regulatory experience desirable
  • Basic understanding of the medical device industry, including Quality Management Systems, and international regulatory fundamentals.


STERIS is a leading provider of products and services that meet the needs of growth areas within Healthcare: procedures, devices, vaccines and biologics.  We exist to fulfill our MISSION TO HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD. STERIS is a $3B, publicly traded (NYSE: STE) company with approximately 16,000 associates and Customers in more than 100 countries.

If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.

STERIS is an Equal Opportunity Employer.  We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law.  We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location’s HR Office during normal business hours.

Req ID:  29750
Job Category:  Regulatory Affairs

Eden Prairie, MN, US, 55344

Nearest Major Market: Minneapolis

Job Segment: Intern, Medical, Quality Manager, Inspector, Medical Device, Entry Level, Healthcare, Quality