Quality Control Process Technical Analyst

Novo NordiskClayton, NC
Onsite

About The Position

You will be joining Fill & Finish Expansions (FFEx), which is responsible for all major expansion activities within aseptic production, solid dosage forms, finished products, fill & finish warehousing, and QC across all production areas in Product Supply. The area is anchored in Product Supply, Quality & IT, which globally employ approx. 20,000 of Novo Nordisk’s 50,000 employees. FFEx is a newly established and growing area with the responsibility to design, plan, and build all new aseptic filling capacity across Novo Nordisk to serve the needs of millions of patients. We do it by rethinking our production facilities with the use of modern technology, as we are setting the standards for the aseptic production of the future. Facilities designed today which we will still be proud of 20 years from now. FF Expansions has a global approach, where you will be working with multiple sites and cultures across the world.

Requirements

  • Bachelor’s degree in science or technical field from an accredited university required or equivalent combination of education and experience required
  • Minimum of five (5) years of QC experience in a pharmaceutical or related (regulated) environment required
  • 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
  • Knowledge & understanding regarding departmental processes & their high-level inter-relationships required (i.e. how they work together to establish a system) required
  • 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

Nice To Haves

  • May consider an Associate Degree in science or technical field from an accredited university required with a minimum of seven (7) years QC experience
  • Leadership/Supervisory experience preferred
  • Demonstrated knowledge of adult learning methodologies & can use multiple methods to train & coach others within the department & organization preferred

Responsibilities

  • 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

Benefits

  • 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
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