Quality Control Analyst II - SDF

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



Perform & review analysis of in-process, release & stability samples in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines.



Relationships



Reports to Senior Manager, QC – OFP.



Essential Functions



Accuracy & Scientific Soundness of Lab Data



Environmental Compliance



GMP Compliance of Laboratory



Maintain testing proficiency for methods



Timeliness of Lab Results & Investigations



Analysis of Samples



Author Deviations



Coaching other analysts



Data Trending & Tracking



Ensure departmental documents are current & standardized



Laboratory Equipment Validation & System support



Laboratory IT System support



Perform deviation & change control activities



Supports Deviations



Systematic Problem Solving



Follow all safety and 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. Ability to do close precision work with their hands. Must be able to remain in a stationary position (sitting and standing) 50% of the time. May require corrected vision to 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.



Minimum Qualifications



Minimum of a Bachelor’s degree in Chemistry or relevant field of study from an accredited university required or an equivalent combination of education and experience



May consider an Associate’s degree in chemistry or relevant field of study from an accredited university with a minimum of three (3) years of experience in a clinical or industrial/pharmaceutical laboratory



May consider a High School Diploma or GED with a minimum of five (5) years of experience in a clinical or industrial/pharmaceutical laboratory



Minimum of three (3) years of experience in a clinical or industrial/pharmaceutical laboratory required



Must demonstrate attention to detail required



Preferred Qualifications



Ability to author scientific & technical reports preferred



Able to perform routine testing per SOP & GMP standards preferred



Change control, deviation, trending a plus



Knowledgeable in GMP & laboratory techniques preferred



Serve as a subject matter expert on QC processes a plus



Strong communication skills (verbal & written) preferred



Troubleshooting for laboratory equipment a plus



Validation & technical transfer experience a plus



Skills or knowledge in the following discipline: Chemistry Analysis of tablets including UPLC and Dissolution 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.