Regulatory Affairs Intern

Embark on an exciting journey at Pulse Medica! Are you interested in learning how innovative medical technologies progress from development to clinical use and, ultimately, commercialization? As a Regulatory Affairs Intern, you'll gain hands‑on experience supporting regulatory activities, product development processes, technical documentation, and cross‑functional projects that help bring cutting‑edge ophthalmic technologies to patients.

Working alongside experts in regulatory affairs, quality, clinical affairs, and engineering, you'll contribute to meaningful projects while developing practical skills in a fast‑paced medical device environment.

Pulse Medica is redefining the landscape of ophthalmic technology by developing breakthrough imaging and laser technologies for ophthalmic disease. Recognized as a Great Place to Work for 4 consecutive years, we've built a culture where innovation thrives and multidisciplinary teams solve complex challenges  technology blends real‑time computer vision, deep learning, and 3D imaging with high‑precision laser systems to create new treatment solutions to prevent vision loss.

By uniting cutting‑edge research with scalable engineering, Pulse Medica is creating treatment solutions that position the company to be at the forefront of the next generation in eye care.

As a Regulatory Affairs Intern, you will support regulatory, product development, and project coordination activities across a variety of initiatives. You will gain exposure to medical device regulations, technical documentation, product development processes, and scientific communications while working closely with multidisciplinary teams.

This position is ideal for students interested in regulatory affairs, clinical research, medical devices, biomedical innovation, or health sciences who are looking to gain practical industry experience.

• Research regulations, guidance documents, and standards relevant to investigational use and future market entry.
• Conduct literature reviews and background research to support regulatory planning and submissions.
• Summarize requirements and maintain regulatory requirements and standards compliance trackers.
• Assist with preparing and compiling regulatory submissions, amendments, responses, and supporting documentation.
• Gather information from engineering, quality, clinical, preclinical, and external partners to support regulatory activities.
• Maintain organized submission files, regulatory correspondence, approvals, and records of regulatory decisions.

• Work with Systems Engineering and other subject matter experts to organize technical documentation, including device descriptions, labeling, instructions for use, and performance evidence.
• Support design control, risk management, and change control processes by tracking required documentation, decisions, and action items.
• Gather information regarding proposed product or process changes and support associated documentation reviews.
• Assist with drafting and updating SOPs, work instructions, templates, and other development‑related documents.

• Help maintain project timelines, milestones, deliverables, and action logs for assigned activities.
• Follow up on outstanding inputs, provide project updates, and flag delays or issues requiring attention.
• Prepare meeting notes and track action items through completion.

• Support the preparation of scientific papers, abstracts, conference presentations, posters, and other technical communications by gathering source information, reviewing content for consistency, and coordinating feedback from subject matter experts.

• Cur…