Melville, New York, US
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Manager, Product Registration

Country : USA USA

State : New York

County : Suffolk County

Town : Melville

Category : Marketing

Contract type : Permanent

Availability : Full time

Job description

The Manager will lead a team directly responsible for developing global product registration dossiers in collaboration with local affiliates and cross functional partners across the enterprise.

Team responsibilities include supporting the initial regulatory submission as well as ongoing maintenance and amendment of registrations, development of strategies to bring new products and ingredients to market. To keep pace with the changing regulatory world the team is tasked with integrating new regulations and requirements into product dossiers and communicating new or updated requirements to cross functional partners.

The manager will assess the skills necessary to deliver against project objectives and create training and development plans to ensure the function has the skills necessary to deliver against corporate objectives.

Manage shifting team priorities.
  • Enable others to achieve project goals; provide direction and remove barriers.
  • Prepare and communicate impact assessment of changes in regulation or interpretation to appropriate function(s).
  • Provide regular follow-up with each market to ensure accuracy and sufficiency of data and documentation.
  • Provide oversight and quality review of dossiers (data, documents), identify opportunities for improvement.
  • Develop and share and meaningful updates on registration KPIs with stakeholders
  • Job: Research & Development

    Primary Location: US-NY-Melville

    Job Type: Standard

    Schedule: Full-time

    Shift: 1st (Day) Shift

    Job Number: 2214908

    We are an equal opportunity employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply. It is Company's policy not to discriminate against any employee or applicant for employment on the basis of race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. The Company will endeavor to provide a reasonable accommodation consistent with the law to otherwise qualified employees and prospective employees with a disability and to employees and prospective employees with needs related to their religious observance or practices. Should you wish to apply for this position or any other position with the Company and you believe you require assistance to complete an application or participate in an interview, please contact [email protected]



    • Excellent project management and multi-tasking skills.

    • Strong organizational and analytical skills with attention to detail.

    • Excellent problem solving, organizational, prioritization and time management skills.

    • Team player, able to build, foster and nurture relationships with members of cross-functional teams.

    • Excellent communication and interpersonal skills.

    • Able to communicate complex regulations for non-technical business partners

    • Able to develop and evaluate alternate registration strategies

    • Fully proficient and experienced with Windows Office, Excel and Outlook and computer applications.

    • Demonstrated team building and personnel development skills

    • Minimum Bachelor of Science or Bachelor of Arts with focus on biology, chemistry, biochemistry or toxicology
      Relevant Cosmetics industry experience considered

    • 3-5 years experience

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