Novo Nordisk Hiring for Associate Supply Chain Engineer Job at Clayton, NC Full Time

About the Department

At Novo Nordisk, we want to make a difference. For nearly 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 Clayton, NC, we now operate two adjacent pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains.

Our Clayton, NC Injectable Finished Products (IFP) facility is a 457,000 square foot aseptic “fill and finish” site that is responsible for producing innovative, injectable diabetes and obesity treatments. When you work at IFP, you’ll join a global network of manufacturing professionals focused on several key, final production processes, including sterile formulation, filling, inspection, device assembly and packaging.

At IFP, our employees are passionate about what they do, knowing their work makes a difference to millions of people who rely on our products every day. After all, producing medicines is a special responsibility.

Join Team Novo Nordisk and help us make what matters.

Position Purpose

This strategic role combines aspects of both supply chain & process improvement. Responsible for optimizing the NNPILP Supply Chain through support of data analysis, problem solving & execution of changes including technical improvement projects focused in Planning, Warehousing, Procurement, & Shipping.

Accountabilities

• Support data analysis, problem solving & execution of changes in Planning, Warehousing, Procurement, & Shipping
• Support transformation program strategies & projects in collaboration with Supply Chain management
  • Review, adjust & update the programs according to the progress made on the established governance of the program to ensure: Sharing, monitoring, & control of the program
  • Propose risk mitigation actions
  • Monitoring of the necessary resources needed for execution
• Support continuous improvement projects, drive SPS to closure & identify any anomalies that have arisen & identify corrective actions
• Carry out necessary investigations to optimize/ make operations more reliable
• Provide engineering design support for Supply Chain facility/equipment changes & additions
• Overseas operational training needs & performs training to ensure standards are met
• Responsible for investigation & solution of quality problems in department such as: unscheduled events, deviations, etc.
• Other accountabilities, as assigned

Required Qualifications

BA/BS degree in Engineering or Supply Chain or equivalent combination of education & experience.

Desired Qualifications

• Minimum of two (2) years of manufacturing, supply chain or logistics experience, preferably in a pharmaceutical environment
• Project Management experience
• Experience/exposure to Lean/Six Sigma methodologies & achieving sustainable process improvements
• Knowledge of supply chain systems such as SAP or equivalent
• Knowledge of robotics & automation
• Knowledge of US, EU regulations & guidelines, & application of GMP’s
• Ability to communicate technical information clearly in writing & presentations
• Planning, organizing, managing execution, checking results, & revising work plans
• Strong communication skills across multiple organizational levels

Physical & Other Requirements

• Occasionally moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions
• Constantly operates a computer & other office equipment using hands
• Must be ability to remain in a stationary position 50% of the time
• Handles transport of hazardous materials
• Occasionally performs critical job functions in extremely cold work environments
• Ability to work in loud noise environments with hearing protection
• Ability to travel internationally, as requested (up to 10%)
• Ability to work in an open office environment with the possibility of frequent distraction
• Ability to work the hours necessary to support a 24/7 continuous manufacturing operation
• Ability to adjust work schedule to work with colleagues in other international time zones

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.

Novo Nordisk requires all new hires to be fully vaccinated against COVID-19 prior to the first date of employment. As required by applicable law, Novo Nordisk will consider requests for reasonable accommodation.

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.