Description
Job Overview with Visa Sponsorship
Are you a regulatory affairs professional looking for an exciting career opportunity in Canada? We are offering a regulatory affairs job in Canada with visa sponsorship, providing you with the chance to contribute your expertise to the pharmaceutical, medical device, or biotechnology industries in one of the most diverse and regulated healthcare markets in the world.
Job Details:
- Employer Name: BC Hydro
- Position: Regulatory Affairs
- No of Vacancies: 1
- Salary: $45.00 hourly / 20 to 40 hours per week
- Employment Type: Full-time, Part-time
- Location: Canada
Education
- No degree certificate or diploma
Experience
- 3 years to less than 5 years
Job Responsibilities
As a regulatory affairs specialist in Canada, your responsibilities will include:
- Regulatory Compliance: Ensure products comply with Canadian regulatory requirements and international standards.
- Product Registration: Prepare and submit regulatory submissions for product approvals and maintain product licenses.
- Documentation Management: Manage and maintain regulatory documentation, including technical files, dossiers, and submissions.
- Labeling and Packaging: Review and approve product labeling and packaging to meet regulatory guidelines.
- Quality Assurance: Collaborate with quality assurance teams to ensure compliance with GMP (Good Manufacturing Practices) and other quality standards.
- Regulatory Strategy: Develop and implement regulatory strategies to support product development and market access.
Qualifications/Skills
To excel in this role, you should possess the following qualifications and skills:
- Bachelor's degree in a relevant field such as pharmacy, life sciences, or regulatory affairs.
- Strong knowledge of Canadian and international regulatory requirements.
- Excellent written and verbal communication skills.
- Attention to detail and ability to manage complex regulatory documents.
- Problem-solving and critical-thinking abilities.
- Proficiency in regulatory software and databases.
Education and Experience Requirements
- Education: Bachelor's degree in pharmacy, life sciences, regulatory affairs, or a related field is typically required. Advanced degrees or regulatory certifications are a plus.
- Experience: A minimum of [X years] of relevant experience in regulatory affairs within the healthcare industry is preferred.
Working Environments
You will work in the dynamic and highly regulated healthcare industry in Canada, which includes pharmaceutical, medical device, and biotechnology sectors. Canada's healthcare industry is known for its commitment to safety, innovation, and rigorous regulatory standards.
How to Apply
Apply on the company website
FAQ
1. Is visa sponsorship available for international applicants?
Yes, we offer visa sponsorship for eligible international applicants, facilitating legal work in Canada.
2. What is the typical work schedule for regulatory affairs professionals in Canada?
Work schedules may vary depending on the employer and specific projects. Typically, it follows standard business hours, but additional hours may be required to meet regulatory deadlines.
3. Are there opportunities for career advancement in regulatory affairs in Canada?
Yes, Canada's healthcare industry offers various opportunities for career growth, including senior regulatory roles, management positions, and specialization in specific therapeutic areas.
Conclusions
Join Canada's healthcare industry as a regulatory affairs specialist and play a vital role in ensuring product safety and compliance. With visa sponsorship and a commitment to regulatory excellence, you can become an essential part of the healthcare regulatory landscape in Canada. Apply now to contribute your expertise to the dynamic Canadian healthcare market.