Regulatory Affairs Specialist - 12 month contract

KNOWLEDGE/EDUCATION

• BSc. in one of the biological or chemical sciences.

JOB EXPERIENCE

• Minimum of 5 years relevant experience in Regulatory Affairs in the medical devices industry. 

QUALIFICATIONS

• Excellent knowledge of the Food and Drugs Act and Regulations.
• Experience in the preparation and filing of medical devices and drugs submission.
• Excellent knowledge of the Natural Health products Regulations.
• Team player with very strong interpersonal skills.
• Strong problem solving and organizational skills and able to work with minimum supervision. 
• Detail oriented, accurate, and results driver.
• Ability to manage multiple priorities in a fast-paced environment.
• Must be computer literate using Microsoft software (i.e. Word, Excel, PDF, etc.).  Knowledge of JDE and/or SAP is an asset.
• Excellent verbal and written communication skills.
• Must be bilingual.

DISCLAIMER

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this job.  It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job.

Medtronic of Canada strives through our vision to build a culture of inclusiveness through our commitment to employment equity and diversity. Discrimination is prohibited on any grounds protected under the Canadian Human Rights Act. Employment applications are encouraged from all members of our community. Upon request, candidates with disabilities will be accommodated during the recruitment process.