Quality Control Process Technical Analyst

Company: Novo Nordisk
Location: Clayton
Posted on: July 10, 2025

Job Description:

About the Department At 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 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 Provides support to Quality Control (QC) by driving continuous improvement, optimization, and innovation as well as leading systematic problem solving and change requests. Works with members of the departmental leadership team to share best practices with NN departments/sites & external vendors. Based on assigned area of responsibility, may work with LIMS and/or QC initiatives. Relationships Reports to Manager, QC Support. Essential Functions Serve as QC Global LIMS Site SuperUser and QC Static Builder responsible for training and building of QC methods Responsible for driving continuous improvement, innovation, and optimization projects Responsible for driving change requests and assisting with large scale investigations (QMT) Lead & coach peer analysts and leaders in problem solving for small-scale process & quality issues Understand the processes of data evaluation and trending, to include reporting findings to leadership Represent QC on global level and interact/collaborate with other NN sites 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. 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 required corrected vision to 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. Qualifications Bachelor’s degree in science or technical field from an accredited university required or equivalent combination of education and experience required May consider an associate degree in science or technical field from an accredited university required with a minimum of seven (7) years QC experience Minimum of five (5) years of QC experience in a pharmaceutical or related (regulated) environment required Leadership/Supervisory experience preferred Demonstrated foundational understanding of processes, procedures & products associated with assigned areas required Perform detailed analysis of events & processes, develop appropriate responses to situational needs, & convey information/results to various organizational levels as appropriate required Demonstrated knowledge of adult learning methodologies & can use multiple methods to train & coach others within the department & organization preferred Knowledge & understanding regarding departmental processes & their high-level inter-relationships required (i.e. how they work together to establish a system) Excellent verbal & written communication skills, investigative writing skills, & computer skills (MS Word, Outlook, Excel, PowerPoint, & LIMS) required Demonstrates ability to manage multiple tasks/deadlines & prioritize properly based on process needs & events required 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.

Keywords: Novo Nordisk, Rocky Mount , Quality Control Process Technical Analyst, Science, Research & Development , Clayton, North Carolina