Through Innovation, Creativity and Excellence, Trudell Medical International (TMI) employees help people around the globe breathe easier. Our unwavering commitment is evidenced in the products we create, the innovations we generate and the standards of excellence we deliver.
 
TMI employees harness the power of our innovative spirit to relentlessly pursue creative new opportunities and secure sustainable growth.  Advanced product design, research in aerosol science, and cleanroom manufacturing of medical devices provide fulfilling work environments for our multidisciplinary team of professionals.
 
We’re actively searching for our next Regulatory Affairs team member for the position of:
   
As a member of our Regulatory Affairs team you will provide accurate, relevant, and timely information internally and externally, to maintain product regulatory compliance, and to support approval of regulatory submissions for global product markets.
 

• Have you earned a college diploma or university degree in health or biological sciences, or equivalent field, along with a certificate in Regulatory Affairs?

 

• Have you gained two years regulatory experience in a medical device environment?

 

• Do you possess excellent oral and written communication skills, and have experience with technical writing?

 

• Do you have strong interpersonal skills with the ability to communicate effectively with internal personnel and external parties?

 

• Are you detail oriented?

 

• Do you have knowledge of the requirements of an ISO 13485 quality program?

 

• Have you gained knowledge of the regulations governing medical devices in Canada, US and Europe?