Director, Regulatory Affairs

Job Description
POSITION OVERVIEW
For the LVMH Beauty scope of brands, joining the Regulatory Affairs & External Relations team to lead the operational regulatory affairs team on cosmetics and OTC drugs. This role will be the contact to various governmental agencies in the USA and Canada. This position will be an expert for operationalizing new laws and regulations pertaining to cosmetics and OTC drugs for the USA and Canada. They will also be the lead on scientific topics at the US and Canadian trade associations
Ideal candidate is a self-starter, process creator and executor,  natural problem solver, highly creative and flexible to bring solutions in a complex regulatory environment.
Leading a team
Position is full time
Position is hybrid, in person
Position may require up to 20% domestic and/or international travel
PRINCIPAL DUTIES AND RESPONSIBILITIES
For LVMH Beauty scope of brands…
Fluent knowledge on the cosmetic and OTC drug business, and regulatory implications in gaining and maintaining market access in the USA and Canada.
Identifying and actioning opportunities on operational regulatory affairs topics to drive our Beauty business on cosmetic and OTC drug regulations.
Demonstrate broad business thinking, routinely monitors, and keeps current on competitive market trends, competitor and health authority activity to identify opportunities and risk to assigned business areas.
Working with Strategy and Advocacy regulatory team to evaluate operational impact specific to LVMH Beauty Maison’s for the regulatory evolution in the USA and Canada on notifications, registrations or labeling and sharing information within the Group. Creating a proposal and ensuring its followed.
Lead on operational questions linked to regulations of cosmetics and OTC drugs.
Strong leadership and ability to drive process internally on how to prepare, submit, maintain records, and produce KPI’s for USA and Canada for the following:prior to product launch (MoCRA, CNF, CA Safe Cosmetic Act, children’s products etc.)
annual notification if needed (VOC, packaging/extended producer responsibility, CARB, and any other states)
OTC establishment registration, drug listing, blanket no change with FDA
DIN/NHP registration with Health Canada
Lead and deliver on individual key projects within timelines and in compliance with new and existing regulations and requirements.
Strong people leadership skills to hone regulatory abilities and strategic growth within the team. Ability to coach and harness meaningful talent development.
Provide clear direction to teams on operational impacts of regulations pertaining to cosmetics and OTC drugs.
SUPERVISION RECEIVED
Reports to Vice President, Regulatory Affairs & External Relations
SUPERVISION EXERCISED
(4.5) Individual contributors