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 workplace. 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 creative 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
Robust 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.