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Global Regulatory Affairs Intern at CooperCompanies

Victor, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

29 Jun, 26

Salary

30.0

Posted On

31 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Scientific Principles, Experimental Design, Technical Documentation, Written Communication, Verbal Communication, Detail-Oriented, Organization, Collaboration, Analytical Skills, Critical-Thinking, Microsoft Office, Document Control, Quality Systems, Regulatory Affairs, Initiative

Industry

Medical Equipment Manufacturing

Description

At CooperVision, a division of CooperCompanies, we’re driven by a unifying purpose to help people to experience life’s beautiful moments. We are connected through our shared values - dedicated, innovative, friendly, partners, and do the right thing. As a leading global manufacturer of contact lenses, we are committed to helping improve the way people see each day. Through our diverse lens portfolio, we tackle the toughest vision challenges – including astigmatism, presbyopia, and childhood myopia. We offer the most complete collection of spherical, toric, and multifocal products available, enabling us to fit 99% of all contact wearers. Learn more at www.coopervision.com [https://www.coopervision.com]. Job Summary: The Global Regulatory Affairs (RA) intern will support the development of an improved structure and template for Technical File documentation aligned with current State‑of‑the‑Art regulatory expectations, working closely with Global RA Specialists and Senior Specialists. In addition to focusing on Technical File enhancements, the intern will gain exposure to medical device regulatory requirements, including labeling and promotional material.

Responsibilities

The intern will support the development of an improved structure and template for Technical File documentation aligned with current State-of-the-Art regulatory expectations, working closely with Global Regulatory Affairs Specialists. Additionally, the role involves gaining exposure to medical device regulatory requirements, including labeling and promotional material.