Regulatory Affairs Specialist - Montréal, Canada - vitaltracer
3 weeks ago
Description
Work Term:
Permanent
- Work Language: English
- Hours: 38 to 44 hours per week
- Education: Master's degree
- Experience: 5 years or more
- Bioengineering and biomedical engineering
- Mechanical engineering
Tasks:
- Analyze and provide advice on the managerial methods and organization of an establishment
- Develop quality management and quality assurance standards
- Propose improvements to methods, systems and procedures
- Plan and control budget and expenditures
Supervision:
- 1 to 2 people
Regulatory investigation:
- Regulatory affairs
Computer and technology knowledge:
- Microsoft Visio
- MS Word
- MS Excel
- MS PowerPoint
- MS Outlook
- MS Office
Industrial processes and biological studies:
- Product development
Type of inspection and investigation:
- Medical devices
Area of work experience:
- Medical instruments and devices
- Research and development
Medical specialization:
- Biomedical engineering
Area of specialization:
- Risk management
- Internal audit
Personal suitability:
- Efficient interpersonal skills
- Flexibility
- Team player
- Time management
Screening questions:
- Are you currently legally able to work in Canada?
- Are you willing to relocate for this position?
- Do you currently reside in proximity to the advertised location?
- Do you have previous experience in this field of employment?
- Do you have the aboveindicated required certifications?
- Do you have the necessary equipment for remote work (i.e. internet, home office, etc.)?
- What is the highest level of study you have completed?
- What is your current field of study?
- What is your current level of study?
Health benefits:
- Health care plan
Financial benefits:
- As per collective agreement
Long term benefits:
- Longterm care insurance
Other benefits:
- Learning/training paid by employer
- Team building opportunities
- Parking available
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