About the Department

At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. 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 legacy Injectable Finished Products (IFP) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. At IFP, you’ll join a global network of manufacturing professionals who are passionate about what they do.

What we offer you:

• Leading pay and annual performance bonus for all positions
• All employees enjoy generous paid time off including 14 paid holidays
• Health Insurance, Dental Insurance, Vision Insurance – effective day one
• Guaranteed 8% 401K contribution plus individual company match option
• Family Focused Benefits including 12 weeks paid parental & 6 weeks paid family medical leave
• Free access to Novo Nordisk-marketed pharmaceutical products
• Tuition Assistance – reimbursement up to $10,000 annually
• Life & Disability Insurance
• Employee Referral Awards

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.

Position Purpose

Enable & inspire NNPII to "live cLEAN®" by driving continuous improvement (CI) mindset throughout the site; providing cLEAN® tools, training, & expertise; leading CI projects & initiatives; & partnering with the organization at all levels.

Accountabilities

• Assist site leaders to develop CI plans; identify, prioritize, & initiate CI opportunities; follow-through on CI activities
• Provide coaching for site leaders & team members to develop the cLEAN® mindset
• Provide SPS support through coaching and facilitating
• Develop, lead, &/or facilitate CI kaizen workshops, problem solving workshops
• Communicate across site to share best practices, success stories, ideas; collaborate across DFP & PS sites as appropriate
• Assist in formal training in NNPII cLEAN® Academy STAR® program
• Provide coaching & mentoring for 1-Star & 2-Star project leaders across site; develop coaching skills
• Manage/Lead focused cross-functional CI projects
• Apply PDCA/DMAIC methodologies to achieve significant, measurable improvement in business, support, & production processes
• Provide direction, coaching, & mentoring for project team members
• Manage/Lead cLEAN® site initiatives
• Develop & lead change management plans for CI initiatives; develop control plans intended to sustain improvement gains
• Provide expertise to site in a variety of other areas (as appropriate): statistical & data analysis, MS office products, project management, change management, etc.

Required Qualifications

• BS/BA engineering, science, statistics, business, or other related field (MS/MA preferred); or equivalent experience + education
• Demonstrated competency (knowledge) in 8 Wastes, Yamazumi, SMED, H.O.C., Pull Systems, Takt Time, LEAN Layout, Standardized Work, & 5S:
  • Demonstrated ability to lead others in application (proficiency) in 50% of the above or equivalent
  • Demonstrated ability to transfer knowledge to others (mastery) in 25% of the above
• Demonstrated coaching, communication, change management, & leadership skills
• Demonstrated flexibility, adaptability, agility, credibility, & change management skills

Desired Qualifications

• 5+ years of experience in manufacturing, maintenance, quality assurance, engineering, supply chain, process improvement
• 3+ years of direct work experience in LEAN &/or Six Sigma
• Demonstrated expertise in pharmaceutical or related industry
• Certification & demonstrated experience/results as cLEAN® 3-Star &/or Six Sigma Black Belt
• Strong computer skills, including experience in MS Office, MS Project, AutoCAD, statistical analysis software, or other related software packages
• Proven expertise in planning/organizing, managing execution, checking results, & revising complex, cross functional projects
• Proven leadership skills

Physical & Other Requirements

• Ability to lift up to 40 lbs. with assistance
• Ability to work in confined spaces & near operating equipment
• Ability to work in loud noise environments
• Ability to work hours necessary to support production & maintenance activities

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.