Manufacturing Operator I - Future 2nd Shift

About the Department

For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. 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 NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Emerging Technologies - Oral Finished Products facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. OFP maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies.

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 12 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
• Monday - Thursday 10hr shift schedule 

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

Efficiently, effectively & safely clean, setup & operate manufacturing equipment to achieve production goals, while adhering to applicable cGMPs & SOPs.  Note: Future 2nd shift position.  The operator will work day shift from 6a-4:30pm until production is moved to 2nd shift in 2025. 

Relationships

Shift Manager.

Essential Functions

• Setup, operate, monitor & control equipment, systems & processes
• Clean & sanitize manufacturing, filling & packaging rooms & equipment per SOPs
• Execute production schedule to achieve production goals
• Handle labeling & components correctly; transferring, counting, FIFO, returns, etc
• Participate actively in & support event response
• Review & author SOPs & other documents as required
• Identify, report & resolve quality issues
• Execute &/or 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 expertise (with the appropriate experience & skill level)
• Record/review production data in BPR & associated forms
• Follow all safety & environmental requirements in the performance of duties
• Other accountabilities, as assigned

Physical 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 color 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.

Qualifications

• High School Diploma or GED required
• Associate’s degree preferred
• Minimum of one (1) year of experience in a manufacturing industry preferred or may consider a completed BioWorks/BioBlend Certificate, military experience or a current contingent worker with three (3) months of demonstrated performance in the role/relevant area in lieu of work experience
• FDA regulated industry & solid dose manufacturing experience preferred
• Ability to read, write & understand complicated product documentation & standard operating procedures with attention to detail required
• Computer literacy including use of Microsoft Office suite programs required
• Some basic mechanical skills preferred
• Must be able to work day shift hours until 2nd shift starts in 2025

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.

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.