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Business Transformation Manager - Nutrition Science and Regulatory Affairs

Pharmavite
West Hills, United Statesfull_timeVerifiedPosted 30 May 2024
💰 $215,353/yr($143,603/yr$215,353/yr)

About the role

HELP US BRING THE GIFT OF HEALTH TO LIFE.

Working at Pharmavite is an experience like no other. With a focus on complete nutrition for all, each endeavor is urgent and every day counts. You'll have the opportunity to work on the #1 selling national vitamin and supplement brand, Nature Made, as well as an exciting portfolio of other products that are shaping the future of the healthy living industry. Consumer-driven innovation, high quality products and a promising portfolio, all driven by a team with a shared sense of purpose -- that's Pharmavite. Join us to bring the gift of health to life.

**Relocation Benefits Available** **No Sponsorship Available**

The Business Transformation Manager Nutrition Science and Regulatory Affairs serves as a generalist providing nutrition science and regulatory support to the business transformation team to ensure scientific due diligence, regulatory compliance, and deliver key goals and strategies. They have a breadth of nutrition science knowledge and knowledge of regulations pertaining to dietary supplements that can be leveraged across product portfolios and ingredient categories (botanicals, vitamins, minerals, and other areas of nutrition). The BT manager identifies opportunities to build process efficiencies, optimize formulas, claims, raw material sourcing, and packaging. Develop & ensure scientific evidence supports product safety and efficacy through scientific due diligence. Lead the identification and investigation of new ingredients and technologies for new products and other business initiatives that support business strategies and objectives. They will develop a small team that works fluidly with the business to deliver results. Reports to Director of Nutrition Science. 

Key Responsibilities 

Critical contributions this role is counted on to deliver include: 

  • Serve as science and regulatory subject matter expert on business transformation team and deliver timely results. 

  • Contribute new ideas to the business transformation team that drives product, portfolio, and process improvements through technical insights. 

  • Provide scientific analysis/interpretation, due diligence, and technical fortitude for product formulations, labeling and advertising claims, consumer, and trade promotions. 

  • Assessment of ingredients, formulas, claims, labeling (labels, advertising, website, ecommerce, social media, etc.) to ensure compliance with domestic and international regulations and Pharmavite policies.   

  • Develop & manage a small team of scientists that actively and consistently contributes new ideas to drive consumer health through scientific and technical insights. 

  • Collaborates with Nutrition Science and Regulatory Affairs teams to monitor emerging issues, analyze implications of changing science and regulations, and provides guidance to the business transformation team. 

Critical Success Factors 

You’ll be most successful in this role if you have: 

  • Excellent oral and written communication skills, including confidence with public speaking and engagement with presenting to employees, customers, and scientific peers. 

  • Ability to apply strong knowledge of physiology and nutrition science to meet consumer needs. 

  • Demonstrated skills in critical analysis of scientific results, and translation of scientific results to claims. 

  • Demonstrated skills in collaborating cross-functionally, prioritization, time management, and project management from planning to delivery of results. 

  • Ability to continually integrate new learnings with existing knowledge. 

  • Ability to convey technical issues and productively interact with non-scientists.

Capabilities & Skills Required 

In order to take on these challenges, you’ll need to have: 

  • A Master’s degree plus a minimum of 7 years of experience in scientific studies evaluation for product claim development, clinical trial design, development, and execution is required.   

  • A PhD, MD, DO, or PharmD degree plus a minimum of 4 years of experience in scientific studies evaluation for product claim development, clinical trial design, development, and execution is required.   

  • Preferred, 3 or more years of US regulatory experience with an emphasis in dietary supplements. 

  • Previous experience with cross-functional collaboration with key internal stakeholders is required. 


OUR OFFER

Here, career paths aren't predefined, and bureaucratic limitations don't exist -- you have the opportunity to grow, learn from industry pioneers, and develop the way you want to. Pharmavite is investing more in the development of our team -- to help us deliver on our purpose and help you achieve your

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Pharmavite

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