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

　　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.

　　The Position

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

　　Relationships

　　Reports to Manager.

　　Essential Functions

　　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

　　Develop, lead, &/or facilitate CI kaizen workshops, problem solving workshops, failure investigations

　　Communicate across site to share best practices, success stories, ideas; collaborate across DAPI-US, DFP & PS as appropriate

　　Provide formal training in cLEAN® programs across the site

　　Provide coaching & mentoring for 1-Star, 2-Star & 3-Star project leaders across site

　　Manage/lead complex cross-functional CI projects

　　Apply PDCA/DMAIC/DICOB methodologies to achieve significant, measurable improvement in business, support, & production processes

　　Support in directing, coaching, & mentoring for site 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.

　　Follow all safety & environmental requirements in the performance of duties

　　Other accountabilities, as assigned

　　Physical Requirements

　　Ability to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time. (% can change on a case by case basis based on the role.

　　Qualifications

　　Bachelor’s degree in Engineering, Science, Statistics, Business, or a relevant field of study from an accredited university required

　　Minimum of five (5) years of experience in manufacturing, maintenance, quality assurance, engineering, supply chain, process improvement required

　　Certification & demonstrated experience/results as cLEAN®2-Star &/or Six Sigma Green Belt required; certification in cLEAN® 3-Star &/or Six Sigma Black Belt preferred

　　Demonstrated expertise in Six Sigma,cLEAN®, & change management preferred

　　Demonstrated coaching, communication, change management, & leadership skills preferred

　　Strong computer skills, including experience in MS Office, MS Project, AutoCAD, statistical analysis software, or other related software packages preferred

　　Demonstrated flexibility, adaptability, agility, credibility, & change management skills required

　　Proven expertise in planning/organizing, managing execution, checking results, & revising complex, cross functional projects preferred

　　Proven leadership skills preferred

　　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.