Launch your career at PulseMedica as a Regulatory Affairs Intern. Gain hands-on experience in medical device regulations, product development, and project coordination in a hybrid work environment. This internship is perfect for students in Health Sciences or Biomedical Engineering.
You'll be engaged in regulatory activities, technical documentation, and collaborate with multidisciplinary teams on cutting-edge ophthalmic technologies. This role is ideal for those looking to deepen their knowledge in regulatory affairs, clinical research, and healthcare innovation. Key Responsibilities:
- Research regulations and standards for market entry
- Conduct literature reviews to support regulatory submissions
- Maintain compliance trackers for regulatory requirements
- Organize technical documentation with engineering teams
- Assist in preparing scientific papers and presentations
Requirements:
- Currently enrolled in or graduated from relevant programs
- Interest in clinical research and healthcare innovation
- Strong technical writing and organizational skills
- Detail-oriented and willing to learn
- Must be legally entitled to work in Canada
Empower your career while contributing to groundbreaking advancements in eye care at PulseMedica.