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Vice President, Quality Control

12 years
Not Disclosed
10 Sept. 11, 2025
Job Description
Job Type: Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Director – Quality Control
Location: Clayton, North Carolina, United States
Job Category: Quality


About Novo Nordisk

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.


What We Offer

  • 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


Position Overview

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


Key Responsibilities

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


Qualifications

  • 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


Physical Requirements

  • Ability to work in an open office environment with potential distractions

  • Travel up to 10% of the time


Our Commitment

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.