Pharma QA Specialist: AI-Powered Quality & Compliance

Novo Nordisk A/S

Kalundborg

Remote

DKK 570,000 - 838,000

Full time

26 hours ago
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Job summary

Novo Nordisk A/S in Kalundborg is seeking an experienced QA professional to provide proactive, risk-based QA oversight across daily production. You will review batch documentation, deviations, change requests and SOPs while supporting audits and continuous improvement initiatives.

The role requires a strong quality mindset, two-plus years in QA or production in pharma, and excellent collaboration and communication skills in English.

Qualifications

  • Hold a relevant academic degree in pharmacy, veterinary medicine or related natural science.
  • Experience in the pharmaceutical industry with at least 2 years in QA or production.
  • Strong quality mindset with a risk-based approach.
  • Willingness to simplify, optimize and continuously improve.
  • Curious about digital tools and responsible AI in quality processes.
  • Adaptable and able to maintain quality when priorities change.
  • Proactive learner and developer.
  • Inclusive team player with strong collaboration and communication.
  • Proficient in written and spoken English.

Responsibilities

  • Provide proactive, risk-based QA oversight of processes and documentation for daily production.
  • Review and approve deviations, change requests, trend reports and SOPs.
  • Provide visible QA support on the shop floor.
  • Support timely resolution of quality-related issues.
  • Identify trends, risks and opportunities for improvement.
  • Simplify and optimize processes while maintaining compliance and product quality.
  • Support internal audits and inspections by health authorities, including presenting QA data.

Skills

Quality mindset
English proficiency
Team collaboration

Education

Pharmacy / veterinary medicine / natural science degree

Job description

Novo Nordisk A/S in Kalundborg is seeking an experienced QA professional to provide proactive, risk-based QA oversight across daily production. You will review batch documentation, deviations, change requests and SOPs while supporting audits and continuous improvement initiatives.

The role requires a strong quality mindset, two-plus years in QA or production in pharma, and excellent collaboration and communication skills in English.

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