Novo Nordisk Manufacturing Process Technician I - Night Shift in Clayton, North Carolina
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.
Operate FlexPen Assembly/Packaging manufacturing equipment in order to achieve production goals.
Set up, operate, monitor & control equipment, systems & processes associated with FlexPen Assembly/Packaging lines
Execution of production schedule to achieve production goals
Maintain aseptic areas & perform sanitizations & environmental monitoring
Actively participate in & support event response
Review & author Standard Operating Procedures (SOP’s) & other documents, as required
Assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance
Train fellow employees in areas of expertise & aggressively learn systems & equipment outside of own area of expertise
Record/review production data in BPR’s & associated forms
Follow all safety & environmental requirements in the performance of duties
Other accountabilities, as assigned
High school diploma or equivalent required (AAS degree in related field preferred)
Minimum of one (1) year experience in manufacturing industry, Food & Drug Administration (FDA) regulated preferred
Ability to read, write & understand complicated product documentation & standard operating procedures with attention to detail
Proven expertise in planning/organizing, managing execution, checking results & revising work plans
Physical & Other Requirements
Ability to move equipment and/or supplies weighing up to 50 pounds within the facility using various body positions
Routinely operates & inspects manufacturing equipment using hands
Ability to be on feet for up to a 12-hour shift
Corrected vision to 20/30
Occasionally ascends/descends a ladder to service equipment; ability to work atop elevated positions
Occasionally works around odorous and/or hazardous materials. May be required to wear latex gloves
Occasionally positions self within confined spaces for inspection, repair & maintenance of equipment
Ability to work in loud noise environments with hearing protection
Ability to attain clean room gowning certification & work with hazardous materials including sanitants
Frequent bending, stooping & prolonged working overhead
Ability to work the hours necessary to support a 24/7 continuous manufacturing operation
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.