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 innovative 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.
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Regulatory Affairs Internship at PulseMedica