Regulatory Affairs Specialist

3 settimane fa


Agordo, Veneto, Italia EssilorLuxottica Group A tempo pieno

About the Role

The EssilorLuxottica Group is seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our Group Quality Regulatory Team, you will work closely with cross-functional teams to develop and fulfill regulatory documentations and evidences.

Key Responsibilities:

  • Prepare and submit regulatory documents for product approval, ensuring compliance with regulations.
  • Provide guidance on product development and testing, ensuring safety and efficacy.
  • Monitor industry trends and regulatory changes, ensuring the company remains compliant.
  • Review labeling and promotional materials for accuracy and compliance.
  • Prepare reports for regulatory authorities.

Requirements

To be successful in this role, you will need:

  • A Bachelor's Degree in a scientific field, such as Biochemistry, Chemistry, Engineering, Pharmacy, or Molecular Biology.
  • At least 5 years of experience in a similar role, with a strong history of regulatory submissions for domestic and international markets.
  • Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP).

About Us

At EssilorLuxottica, we are a global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. We bring together the complementary expertise of two industry pioneers to create a vertically integrated business that addresses the world's evolving vision needs.

We are a company that values creativity, entrepreneurship, and individuality. Our people are dedicated to enabling people to 'see more and be more' through our innovative designs and lens technologies.



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