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Process Engineer

Facility:  Quality
Location: 

Clayton, NC, US

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 Diabetes Finished Products (DFP) 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 DFP, 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 DFP, 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

Improve system & equipment reliability for the core processes to meet all customer, business & regulatory requirements through the following activities:

  • People Focus
  • Process Focus
  • Equipment Focus
  • Standards “Gatekeeper”

 

Accountabilities

  • Support technical development of Maintenance Technicians
  • Improve the performance of one production line or system, using process improvement systems in place
  • Lead projects that affect one production line using process improvement systems in place, including project management
  • Support event response activities
  • Maintain standards for procedures & maintenance plans
  • Support DFP global collaboration initiatives

 

Required Education

BS in Engineering/related field or Equivalent.

 

Desired Experience

2-5+ years engineering experience in Maintenance, Design, Cleaning Validation, Clean in Place, Sterilize in Place, Sterilization, Autoclaves, Process Improvement; cLEAN® 1-Star preferred.

 

Technical/Process/Functional Knowledge

Knowledgeable in the following systems:  Instrument & Electrical, Mechanical, Control/SCADA/PLCs, Process Improvement Methodologies, Root Cause Analysis (RCA).

 

Organization/Planning

Proven expertise in planning/organization/execution of maintenance activities, following up on results, & revising the work plan for complex problems being resolved by cross functional teams.

 

Physical Requirements

  • Ability to work in confined spaces & near operating equipment
  • Ability to work in loud noise environments
  • Ability to travel internationally
  • Ability to work hours necessary to support production & maintenance activities

 

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.