Senior Director, OTC Innovation
Mooresville, NC 
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Posted 18 days ago
Job Description
Description

We believe being healthy should not require tradeoffs. SCN BestCo is a leading innovator, developer and manufacturer of Vitamin, Mineral & Supplement (VMS), Over-the-Counter (OTC) and prebiotics/probiotics in enjoyable forms such as gummies, lozenges and chews. With over 50 years of excellence, our team leads the way in changing how consumers make healthier choices. With unique food science expertise and proprietary processes, we've pioneered many firsts. Our passion to create new to the world products has guided and continues to be core to our mission of making health and wellness more enjoyable. Come join us and become a part of our winning formula!

The Senior Director, OTC Innovation leads a technical team focused on expanding the application of confectionary based forms to the Over the Counter (OTC) space, partnering with commercial leadership and large consumer packaged goods (CPG) customers to win in this rapidly expanding space. This senior leader leads the combined research & development (R&D) and analytical laboratory teams to define and deliver a portfolio of monograph / New Drug Application (NDA) products, optimize the innovation process, and develop a high-performance organization.

Essential Duties and Responsibilities

  • Partner with the Commercial team to define the strategy and pipeline to deliver a high value OTC portfolio and effectively engage key customers; defining key design criteria and delivering the technical program that meets them.
  • Define and deliver technology solutions.
  • Combine pharmaceutical and confectionary science to create breakthrough OTC products.
  • Lead the product and analytical development process from ideation to commercialization, working closely with sales, marketing, and operations teams to bring new products to the market and develop customers to meet growth objectives.
  • Collaborate with Value Stream Leaders to successfully scale-up and commercialize products, and drive manufacturing efficiencies while maintaining key design criteria.
  • Actively manage the portfolio/projects, capturing development activities, managing key risks, addressing any resource gaps, and driving key decisions with the team and executive leadership.
  • Optimize and manage the product development process to drive further efficiency and compliance.
  • Define and implement new best-in-class tools, techniques, and approaches that improve technical efficiency.
  • Actively participate with cross-site R&D leadership team to help build a high-performance cross-site culture that fully leverages and develops talent, including supporting the optimization of the company's approach to innovation and improved capabilities.
  • Develop a best-in-class technical organization that combines excellence in drug product development with confectionary science.
  • Cultivate a productive, collaborative environment across different product teams and functional teams.
  • Provide site and company leadership by participating and driving key company initiatives through the Site Leadership Team (SLT).
  • Set a clear vision for the organization and create a winning team to deliver against business goals.
  • Coach, mentor, and educate the organization on New Drug Application and other processes to build capability and ensure the organization is fit for purpose.
  • Define and manage the resources needed to deliver the technical program, including the budget, organizational structure, and infrastructure.
  • Review and analyze proposals submitted to determine if benefits derived and possible applications justify expenditures.
  • Actively develop supplier relationships and leverage consulting firms where necessary to access new capabilities.
  • Negotiate contracts with third parties as needed to access additional capabilities.
  • Travel (up to 30%) to engage with suppliers and development partners as needed, with some international travel possible.

People Leader Responsibilities

The Senior Director, OTC Innovation carries out People Leader responsibilities in accordance with the Company's policies and applicable laws. Responsibilities include:

  • Recruit, hire, train, develop, and mentor department staff, evaluate staff performance, and develop goals and objectives to create an empowered high-performance team and cultivate top talent.
  • Actively develop organizational and individual employee capabilities, creating a culture of continuous improvement to deliver best-in-class results.

Required Qualifications

Education and Experience:

  • Bachelor's degree in a science discipline relevant to pharmaceutical product development (e.g., chemistry, chemical engineering, pharmaceutical sciences, etc.)
  • 15 years' experience in Research & Development with extensive experience developing and commercializing both oral monograph and NDA drug products.
  • 10 years' progressive professional leadership and management experience.
  • Comprehensive experience of OTC product development across 505.B.2/NDAs & monograph drugs in US.

Knowledge, Skills, & Abilities (KSAs):

  • Entrepreneurial spirit and sense of ownership to maximize the value of their business.
  • Ability to effectively engage and drive action with senior leaders internally and externally, including senior customer leaders, executives, and board members across technical areas and the business.
  • Ability to represent the company and products with major FMCG/Pharma/retail customers, to be able to speak their language, communicate and influence.
  • Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents.
  • Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community.
  • Business acumen and agility to apply pharmaceutical insights and approaches to confectionary forms, to quickly adapt to new challenges, and address them.
  • Demonstrated ability to maximize the impact of the team in both technical and cross functional workstreams.
  • Proven ability to coach, mentor and educate the organization on New Drug Application process, to build capability, and ensure the organization is fit for purpose.
  • Ability to integrate multiple technical and business needs to define clear objectives, success criteria, and action steps for programs.
  • Ability to analyze complex data to determine gaps/inefficiencies in processes and drive improvements.
  • Proficiency in Microsoft Office including Excel and Outlook.
  • Demonstrated practical problem solving and trouble shooting skills. Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, musical notes, etc.,) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables.
  • Ability to comprehend and apply principles of advanced calculus, modern algebra, and advanced statistical theory. Ability to work with concepts such as limits, rings, quadratic and differential equations, and proofs of theorems.

Preferred Qualifications

Education and Experience:

  • Master's or PhD in a science discipline relevant to pharmaceutical product development.
  • Experience in food science/ confectionary based product development.
  • Experience in contract manufacturing and branded products.
  • Experience leading analytical method development.
  • Advanced proficiency in Microsoft Office, enterprise resource planning (ERP), and/or customer relationship management (CRM) software.


Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)

 

Job Summary
Company
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
15+ years
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