About The DepartmentAt 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 YouLeading 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
Ensure the safe & effective operation of a work cell while maintaining a high level of focus on Quality. This person has three key roles; Ensure the process performs per plan, confirm standards & solve problems.
Relationships
Reports to Shift Manager.
Essential FunctionsExecute the production plan by leading the operation, monitoring & controlling of equipment, systems, & processes within the work cell
Enforce all safety & environmental requirements in the performance of duties
Help facilitate a productive, engaging, & safe working environment
Setup next Shift for success
Coordinate Maintenance activities, scheduled by Maintenance Planning, supported by Technical Area Specialist
Lead team in Event Response/RCA with assistance from the Process Engineer & Supervisor
Schedule work cell resources, to include breaks, lunches, & other activities
Address any safety, quality, staffing or personnel issues & escalate to the supervisor if necessary
Monitor performance & the completion of training to assure the competency level of work cell team members. Ensure team members are trained to the standard
Responsible for cGMP documentation
Provide performance review input for work cell team members as required by Shift Manager
Spend 20% - 50% of time operating as an operator in the process
Other Accountabilities As AssignedPhysical Requirements
Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Routinely operates & inspects manufacturing equipment using hands. Strap & unstrap pallets using hands. Must be able to be on your feet for up to a 12-hour shift. May require corrected vision to 20/20 or 20/25 based on role. May require colour vision based on role. Occasionally ascends/descends a ladder. May be required to work at elevated heights. Occasionally works around odorous &/or hazardous materials. May be required to wear latex gloves. May perform critical job functions in extremely cold work environments depending on site. May position oneself within confined spaces for inspection if required of the role. Ability to work in loud noise environments with hearing protection. May be required to secure a motorized vehicle license & operate a motorized vehicle based on the role.
QualificationsHigh school graduate or equivalent required, Associate's Degree in related field required
BioWork graduate preferred
Minimum of 2 years experience in a manufacturing industry, FDA regulated required
Qualified to perform operator activities on work cell equipment required
Ability to read, write & understand complicated product documentation & standard operating procedures with attention to detail. Computer literacy preferred
Experience with planning & organizing, managing execution, checking results, & revising the work plan to meet daily work plan targets a plus
Demonstrates a systematic approach to problem solving & troubleshooting. Supports & actively participates in event response activities for the process. Documents problems & works to bring them rapidly to solution 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.
