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Associate Manager, International Regulatory VMS

Reckitt

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Parsippany, NJ
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Job Description

As posted by the hiring company

Job Overview:

Want to play a vital role at Reckitt in driving Vitamin, Mineral, and Supplement innovations, leading international strategies, and building regulatory intelligence across our global network? You will have the opportunity to make an impact Globally.

International Regulatory Strategy Associate Manager, VMS Health

Parsippany, NJ (will also consider Salt Lake City, UT)

Competitive Salary & excellent benefits package

• Responsible for developing multi-market regulatory strategies in alignment with our international commercial strategies.

• Act as regulatory project manager of new product formulations and submissions, working with the International Regulatory Strategy Manager to drive regulatory expertise and understanding throughout the project lifecycle, deliver against targets, and actively communicate risks and progress.

• You’ll play a critical role in our ambitious growth plans, ensuring the achievement of on-time submissions, managing an international network of regulatory colleagues, and building expertise and capabilities in a changing regulatory environment across the world.

• Will be responsible for working on creating and delivering core dossiers/technical files in partnership with broad cross-functional stakeholders.

• Drive action plans to support successful project delivery.

• Track and interpret complex, ever-changing legislation and give feedback on Regulatory Intelligence records.

You’ll succeed because...

You’re intellectually curious and love working in a matrixed environment across different regions and global functional teams. You’re a regulatory professional with technical agility, a strong work ethic and communication skills, and knowledge of regulatory dossiers in the food and supplement space.

You’ll love it because...

You love challenging the norm, have strong problem-solving skills and attention to detail, and enjoy paving new pathways for the VMS Health business. Will be responsible for creating and delivering the core product technical file relating to Health VMS products, working with the technical file authors to ensure consistency and a ‘right first-time’ approach. Our dynamic and ownership-driven culture will help bring the best out of you every day.

Qualifications

  • 2 years in Regulatory experience (Ideally in the Supplement (VMS) space)
  • International/global experience (i.e., creating dossiers for registrations, liaising with international markets, etc.)
  • Ability to interpret regulations
  • Experience with building regulatory strategies
  • Ability to thrive in a fast-paced environment
  • Familiarity with registration processes (as this is a global role) preferred

Equality

All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.