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Regulatory Affairs Associate
 

Kelly Services just received an opening for a Regulatory Affairs Associate in Markham, Ontario.  This is a one-year assignment, 37.5 hours per week. 

 

Responsibilities include:

  • Build and maintain collaborative working relationships with local/global business partners by ensuring effective and timely communication of regulatory issues, project status and timelines.
  • Execute appropriate regulatory submission for product lifecycle management for medical devices currently marketed in Canada.
  • Management of multiple regulatory projects by ensuring accurate tracking and documentation of activities.
  • Accurate documentation and record keeping of all assigned regulatory activities.

 

Requirements:

  • BS in life sciences is required; advanced degree (MSc or PhD) an asset.
  • Sound knowledge of Food and Drugs Act and Medical Device Regulations and relevant policies and guidelines is required.
  • Excellent verbal and written communication skills.
  • Strong project management and time management skills.
  • Detail-oriented and ability to multi-task.
  • Excellent analytical problem-solving skills.
  • Proficient with Microsoft Office tools.

 

Preferences:

  • Completion of Post Graduate training in Regulatory Affairs - RAC (Regulatory Affairs Certification) preferred.
  • Regulatory affairs experience in preparation of medical device submissions is preferred.
  • Experience in managing regulatory submission activities is preferred.

 

If you are interested, please send me a recent MS Word resume.  We are limited to two submissions at this time so please don’t delay!

Job Ref: CA768JGR000039
Submitted: 10-10-2019 01:00 PM
Location: Ontario - Markham and area
 


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