Job Title: Director – Quality Control
Location: Clayton, North Carolina, United States
Job Category: Quality
For more than 100 years, Novo Nordisk has been a global leader in diabetes care. Our mission is to improve the quality of life for millions of people worldwide. At our North Carolina sites, we operate three pharmaceutical manufacturing facilities, including the Product Supply Aseptic Manufacturing (PS AM) facility in Clayton. This 457,000-square-foot aseptic “fill and finish” site produces innovative injectable treatments for diabetes and obesity.
At Novo Nordisk, employees join a global network of manufacturing professionals passionate about making a difference.
Competitive salary and annual performance bonus
Generous paid time off including 14 holidays
Health, dental, and vision insurance effective from day one
Guaranteed 8% 401(k) contribution with optional company match
Family-focused benefits including 14 weeks paid parental leave and 6 weeks family medical leave
Free access to Novo Nordisk-marketed pharmaceutical products
Tuition assistance, life & disability insurance, and employee referral awards
Career growth opportunities with mentorship and development resources
The Director of Quality Control leads the Quality Control organization to support the production of Novo Nordisk products and devices through testing programs that meet or exceed business, regulatory, and customer requirements. The role includes overall responsibility for Chemistry, Microbiology, Physical Testing, Raw Material testing, laboratory equipment, personnel, facilities, and budgets. This position also supports analysis of samples for NNPILP production sites and contract manufacturers.
Reports To:
Corp Vice President (CVP) & Site Head – Product Supply Aseptic Manufacturing (PSAM)
Coordination with CVP API, VP Oral Finished Product (OFP), and CVP ManDev
Leadership & Strategy
Lead strategic and tactical activities for Quality Control across NNPILP sites
Set direction, track progress, and provide feedback to managers and directors
Foster innovation, collaboration, and continuous improvement in QC processes
Participate in setting plant goals, objectives, policies, and continuous improvement projects
Operational Oversight
Oversee daily QC operations and ensure a healthy, engaged work environment
Ensure accuracy and scientific soundness of laboratory data
Maintain GMP compliance of QC laboratories and processes
Oversee Laboratory Information Management Systems (LIMS) and process improvements
Ensure timely laboratory results to meet batch release KPIs
Manage lab equipment, facilities, method revalidations, and transfers
Compliance & Investigations
Contribute to site GMP compliance
Lead critical investigations (e.g., failures/CAPAs) with thorough root cause analysis and preventive actions
Ensure weekly process confirmations for compliance with local and global standards
Financial & Business Management
Develop long- and short-term business strategies and oversee implementation
Prepare and allocate budgets, identify cost-saving opportunities, and drive revenue growth
Monitor industry trends, competitors, and best practices
People Development
Supervise managers and directors, ensuring Individual Development Plans (IDPs) are in place
Provide coaching, feedback, and mentorship to enable career growth and succession planning
Ensure adherence to Novo Nordisk policies, procedures, and the Novo Nordisk Way
Bachelor’s degree in Chemistry, Microbiology, or relevant field; Master’s preferred
Minimum 12 years of pharmaceutical quality experience, preferably with laboratory experience in sterile products
Minimum 10 years of leadership experience, with at least 5 years managing managers in a manufacturing environment
Knowledge of GMPs, USP/EP/JP compendia, and API production
Experience with method validation and/or transfer preferred
Proven ability to handle complex issues, present technical information, and drive business impact
Ability to work in an open office environment with potential distractions
Travel up to 10% of the time
Novo Nordisk is an equal opportunity employer. We provide inclusive recruitment processes and ensure equality of opportunity for all applicants, regardless of race, ethnicity, religion, sex, gender identity, sexual orientation, disability, veteran status, or other protected characteristics.
We are a modern healthcare company focused on solutions to defeat serious chronic diseases, promote long-term health, and push the boundaries of science to improve millions of lives globally.
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