What are the responsibilities and job description for the cLEAN Partner I position at BioSpace?
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 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 Product Supply Aseptic Manufacturing (PS AM) 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 PS AM, 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 14 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.
Relationships
Reports to Manager
Essential Functions
Assist senior team members to develop Continuous Improvement plans; identify, prioritize, & initiate CI opportunities; follow-through on Continuous Improvement activities
Provide coaching to develop the cLEAN® mindset
Aid in SPS through facilitating & coaching
Support &facilitate CI kaizen workshops, problem solving workshops
Communicate across sites to share best practices, success stories, ideas; collaborate across NNPILP API US, IFP, IFP FFEx & PS sites as appropriate
Assist in formal training in cLEAN® programs across sites
Provide coaching & mentoring for 1-Star project leaders across site; develop coaching skills
Manage/lead focused cross-functional CI projects
Apply PDCA methodologies to achieve significant, measurable improvement in business, support, & production processes
Provide direction, coaching, & mentoring for site team members
Participate in execution of cLEAN® site initiatives
Support change management plans for CI initiatives; develop control plans intended to sustain improvement gains
Follow all safety & environmental requirements in the performance of duties
Other accountabilities, as assigned
Physical Requirements
May move equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. May be required to be on your feet for up to a 12-hour shift. May required corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. May require the ability to work in loud noise environments with hearing protections.
Development Of People Not Applicable
Qualifications
Bachelor’s degree in Engineering, Science, Statistics, Business, or a relevant field of study from an accredited university required
Two (2) years of experience in manufacturing, maintenance, quality assurance, engineering, supply chain, process improvement required
Demonstrated expertise in pharmaceutical or related industry preferred
Certification & demonstrated experience/results as Six Sigma Green Belt is a plus
Demonstrated competency in Lean tools & Lean Principles (Ex.8 Wastes, Yamazumi, SMED, Value Stream Mapping, LEAN Layout, Standardized Work, & 5S) preferred
Demonstrated coaching, communication, change management, & leadership skills preferred
Strong computer skills, including experience in MS Office, Power BI, statistical analysis software, or other related software packages preferred
Demonstrated flexibility, adaptability, agility, credibility, & change management skills preferred
Proven expertise in planning/organizing, managing execution, checking results, & revising complex, cross functional projects preferred
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
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.
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 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 Product Supply Aseptic Manufacturing (PS AM) 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 PS AM, 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 14 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.
Relationships
Reports to Manager
Essential Functions
Assist senior team members to develop Continuous Improvement plans; identify, prioritize, & initiate CI opportunities; follow-through on Continuous Improvement activities
Provide coaching to develop the cLEAN® mindset
Aid in SPS through facilitating & coaching
Support &facilitate CI kaizen workshops, problem solving workshops
Communicate across sites to share best practices, success stories, ideas; collaborate across NNPILP API US, IFP, IFP FFEx & PS sites as appropriate
Assist in formal training in cLEAN® programs across sites
Provide coaching & mentoring for 1-Star project leaders across site; develop coaching skills
Manage/lead focused cross-functional CI projects
Apply PDCA methodologies to achieve significant, measurable improvement in business, support, & production processes
Provide direction, coaching, & mentoring for site team members
Participate in execution of cLEAN® site initiatives
Support change management plans for CI initiatives; develop control plans intended to sustain improvement gains
Follow all safety & environmental requirements in the performance of duties
Other accountabilities, as assigned
Physical Requirements
May move equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. May be required to be on your feet for up to a 12-hour shift. May required corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. May require the ability to work in loud noise environments with hearing protections.
Development Of People Not Applicable
Qualifications
Bachelor’s degree in Engineering, Science, Statistics, Business, or a relevant field of study from an accredited university required
Two (2) years of experience in manufacturing, maintenance, quality assurance, engineering, supply chain, process improvement required
Demonstrated expertise in pharmaceutical or related industry preferred
Certification & demonstrated experience/results as Six Sigma Green Belt is a plus
Demonstrated competency in Lean tools & Lean Principles (Ex.8 Wastes, Yamazumi, SMED, Value Stream Mapping, LEAN Layout, Standardized Work, & 5S) preferred
Demonstrated coaching, communication, change management, & leadership skills preferred
Strong computer skills, including experience in MS Office, Power BI, statistical analysis software, or other related software packages preferred
Demonstrated flexibility, adaptability, agility, credibility, & change management skills preferred
Proven expertise in planning/organizing, managing execution, checking results, & revising complex, cross functional projects preferred
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
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.