Regulatory Affairs Specialist

1 week ago

Markham, Ontario, Canada Kenvue Full time
Regulatory Affairs Intern

Kenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will play a key role in supporting the preparation and submission of regulatory documents, responding to regulatory queries, and maintaining regulatory databases.

Key Responsibilities:
  • Prepare submissions to regulatory bodies, including NHP PLAs, DIN submissions, and Class II medical device applications.
  • Respond to regulatory body queries and provide timely and accurate information.
  • File annual renewal packages to Health Canada and perform assessments to determine regulatory requirements for new projects.
  • Review and approve packaging artwork and advertising materials to ensure compliance with regulatory requirements.
  • Complete environmental ingredient surveys under CEPA and assist in audit preparation.
  • Monitor departmental mailboxes and track communications and commitments to Health Canada.
Qualifications:
  • Enrolled in a post-graduate Regulatory Affairs Certification Program or an undergraduate Science Degree.
  • Excellent communication and interpersonal skills, with the ability to work independently and as part of a team.
  • Strong problem-solving and analytical skills, with the ability to manage multiple priorities and meet deadlines.
What We Offer:
  • Learning and development opportunities to enhance your skills and knowledge.
  • Employee resource groups to support your personal and professional growth.

Kenvue offers a dynamic and supportive work environment, with opportunities for growth and development. If you are a motivated and detail-oriented individual with a passion for regulatory affairs, we encourage you to apply for this exciting opportunity.

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