Manufacturing Operator II

Novo Nordisk • Durham, NC • 4h ago

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 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 -Solid Dosage Forms US 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. SDF 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 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

Operate manufacturing equipment to achieve production goals. Support training for junior team members & demonstrate subject matter expertise in assigned area.

Relationships

Reports to 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

Perform machine changeovers as needed

Handle labeling & components correctly; transferring, counting, FIFO, returns, etc

Actively participate in & support event response

Review & author SOPs, job instructions & 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 area of expertise. (With the appropriate experience & skill level.)

Record/review production data in BPR & associated forms

Participate in process improvement projects to enhance productivity and efficiency

Follow all safety & environmental requirements in the performance of duties

Other duties 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 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.

Minimum Qualifications

High School Diploma or Equivalent required

Minimum of one (1) year of experience in manufacturing environment required

Demonstrated ability to train new hires on processes & technical requirements (SOPs) required

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

Preferred Qualifications

Associate's Degree or BioWorks Certification preferred

Minimum of one (1) year of experience in pharmaceutical solid dose manufacturing or other FDA regulated industry preferred

Demonstrated experience in executing equipment troubleshooting, including restoration of lost function maintenance preferred

Proven expertise in planning/organizing, managing execution, checking results & revising the work plan in accordance with the daily work plan a plus

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.

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