Parfums Christian Dior

Director, Regulatory Affairs

Parfums Christian Dior East Brunswick, NJ

Parfums Christian Dior

Director, Regulatory Affairs

Parfums Christian Dior East Brunswick, NJ

Position

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

Profile

Qualifications & Skills Required

  • Skills
    • Proven leader of driving, negotiating, and executing process
    • Ability to interpret applicable regulations
    • Ability to think and execute creative solutions to complex regulatory issues
    • Ability to think strategically and deliver practical solutions
    • Detail oriented, strong organizational skills, multi-tasking ability, process driven, highly collaborative
    • Ability to meet internal and governmental deadlines
    • High accuracy and reliability on assigned tasks
    • Ability to work to foster a team environment while being able to prioritize work
  • Qualifications
    • Professional experience in Chemistry, Chemical Engineering, Legal or related science
    • 10 years of Cosmetic Regulatory Affairs experience
    • 5 years of demonstrated people-management experience
    • Strong computer skills (PowerPoint and MS Excel)
    • Fluent knowledge of USA and Canada cosmetic regulations
    • Fluent knowledge of USA and Canada drug regulations
    • Fluency or working knowledge of French is a plus
NOTE: This job description is intended to cover the core accountabilities of the position and is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.

LVMH Beauty brands are a M/F, Disabled and Vet EEO/AA Employer.

Additional Information

Hybrid 3x/week at our East Brunswick, NJ office.

LVMH Inc. uses the published salary range as a guideline to provide our employees with market competitive pay while allowing for flexibility to recognize and reward various levels of expertise, performance and tenure.

While the published salary range is a good faith reflection of the targeted salary level for the position, LVMH Inc. reserves the right to pay outside of the published salary range of $160,000.00 - $200,000.00.

This job description is intended to cover the core accountabilities of the position and is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.

All your information will be kept confidential according to EEO guidelines.
  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Job function

    Legal and Finance
  • Industries

    Personal Care Product Manufacturing

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