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Corporate Vice President - Emerging Technologies Solid Dosage Forms

Employer
Novo Nordisk
Location
Durham, NC
Start date
Mar 11, 2025
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Job Details

About the Department

For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world.

 

In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Emerging Technologies -Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. SDF maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies.

 

At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.

 

The Position

Lead and manage Emerging Technologies (ET) / Solid Dosage Forms (SDF) production site in Durham, NC, USA to meet or exceed product supply short- and long-term objectives for production, quality, and financial results according to regulatory requirements, the Triple Bottom Line, and the Novo Nordisk Way of Management. This position will provide the operational and strategic leadership, having the responsibility for directing and overseeing the development, planning, implementation, and maintenance of manufacturing and quality methods, processes, facilities and operations for products and technologies within ET. Overseeing production planning, schedules, materials, equipment, and labor resource requirements as relate to the production and distribution of relevant products.

 

A prominent level of innovation and collaboration with internal and external stakeholders is expected to continuously improve processes and achieve improved operational efficiency for the production and release of products manufactured. Ability to drive and succeed with current business while leading change with a growth mindset.

 

Additionally, responsible for managing external relations with local and state government and other public sector groups, to ensure that the best interests of the organization are represented in the course of public decision-making and that the organization has an excellent reputation and engagement in the community.

 

Relationships

Senior Vice President.

 

Essential Functions

  • Establish and drive vision and strategic operational plan for ET/SDF and NNPILP in alignment with strategic objectives of the company
  • Champions strategic development of site business plans and initiates and leads related Investment / Capital Improvement Projects initiatives
  • Risk management with high focus on minimizing risks for staff, operational and project objectives
  • Oversees site to maximize utilization of employees, equipment, and materials within quality standards
  • Conduct strategic planning, set objectives, and develop performance measures to evaluate and drive site performance in accordance with NN product supply production system
  • Plan, develops and manages annual expense and capital budgets
  • Ability to interact with executive levels, presenting information and proposals to top management, BOD and public forums
  • Internal communication is critical with Denmark headquarters to ensure a clear understanding of product supply objectives worldwide and how these objectives translate into goals and timetables
  • Drives a culture of operational excellence utilizing cLean to increase speed/efficiencies and to reduce waste (costs) and process variation. Manages value improvement programs to maintain superior customer service, reduce costs, and improve quality of our products
  • Recommends operations policies and programs. Approves plant policies consistent with corporate requirements
  • Interacts with other NN groups to support global product requirements
  • Supports other departments to meet the quality and business objectives of NN
  • Responsible for the maintenance and good housekeeping of machinery, equipment, and facilities in accordance with the QSR/cGMP and all global regulatory requirements
  • Foster a culture, ensuring site practices comply with established procedures and meet all local, state or country regulations dealing with environmental, health and safety requirements. Promotes a safe and compliant work environment
  • Assures all activities comply with established company policies and perform all duties in compliance with global regulatory requirements
  • Drive social responsibility and engagement to establish Novo Nordisk as a trusted partner in the community
  • Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations, and industry codes
  • Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others
  • Recruit, hire and develop world class workforce and leadership team to meet all objectives
  • Follow all safety and environmental requirements in the performance of duties
  • Perform other duties as assigned
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    Physical Requirements

    Ability to travel 20-30% of the time, to include international and domestic trips. Ability to work in an open office environment with the possibility of frequent distraction.

     

    Development of People

    Supervisory

    Ensure that reporting personnel have individual development plans (IDP), with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.

     

    Ensure that the IDP forms include completed learning and aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.

     

    Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way.

     

    Qualifications

  • Bachelor’s degree in engineering, science, supply chain management or other relevant field of study from an accredited university required; Master’s degree preferred
  • Minimum of ten (10) years’ experience in a senior management role in biotech and/or pharmaceutical manufacturing environment required, to include exhibition of both strong general management and strategic planning skills
  • Proven process improvement and problem-solving skills, including knowledge of process improvement tools & systems (e.g. LEAN and Six Sigma methodologies) required
  • Working knowledge of FDA regulations relevant to the organization required
  • Proficient with MS Office software required
  • Outstanding written, verbal and public speaking skills in English required
  • Proven expertise in mentoring/development, process confirmation, change management, planning/organizing, managing execution are required
  • Demonstrated ability to review complex organizational plans and provide any required or necessary direction/guidance to ensure success is required
  • Proven negotiation and influencing skills. Commitment to critical internal communication with headquarters in Denmark, to ensure a clear understanding of product supply objectives worldwide and how these objectives translate into OFP-US goals and timetables. Ability to provide regular, clear reporting of results and progress
  • Demonstrated support of vital external communication with the public sector for the exchange of information, to ensure that the best interests of the business, present and future, are accounted for in the course of public decision making
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    We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

     

    At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

     

    Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

     

    If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

    Company

    Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 54,400 people in 80 countries and markets its products in around 170 countries. For more information visit novonordisk.com.

    Our US Research & Development hub, located in the Greater Boston area, brings together the best talent to drive life science innovation. Located in Lexington, Watertown and Cambridge, our teams reflect the full scope of R&D, from early research through late-stage clinical development. We are building for the future by creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. By combining the speed and agility of biotech with the quality, resources, and stability of a large pharmaceutical company, our US R&D hub will benefit from the best of both worlds to develop new medicines that meet the needs of patients.

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    Company info
    Website
    Phone
    617-612-6200
    Location
    75 Hayden Avenue
    Lexington
    MA
    02421
    United States

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