Global Quality Specialist, Pharmacovigilance & Compliance

Freelio; Denmark; On-site; DKK 742,600 - 1,091,600; Full time

Job summary

Novo Nordisk is seeking a Global Patient Safety Quality Specialist based in Søborg, Denmark. You will support GPS processes, provide quality and compliance expertise for the global pharmacovigilance system, and drive improvements across R&D quality.

You will lead quality projects, act as QA for deviations and audits, review regulated documentation, and help shape the governance framework in GPS. This role offers an opportunity to influence quality standards across a global organisation.

Qualifications

• Master's degree in Life Sciences; PhD is an advantage.
• Minimum 6 years of experience in quality assurance or quality management processes.
• Strong experience within drug safety, pharmacovigilance and GxP standards.
• Excellent written and spoken English; ability to translate complexity into clear recommendations.

Responsibilities

• Provide quality and compliance expertise for GPS processes, including the global pharmacovigilance system.
• Lead quality projects and initiatives in R&D to ensure appropriate compliance.
• Act as QA for deviations, change requests, SOPs, inspections and audits.
• Oversee quality compliance within the GPS area.
• Review and approve documentation and records regulated by health authority requirements.

Skills

Quality assurance

Pharmacovigilance

Stakeholder management

English proficiency

Education

Master's Life Sciences

PhD preferred

Job description

Novo Nordisk is seeking a Global Patient Safety Quality Specialist based in Søborg, Denmark. You will support GPS processes, provide quality and compliance expertise for the global pharmacovigilance system, and drive improvements across R&D quality.

You will lead quality projects, act as QA for deviations and audits, review regulated documentation, and help shape the governance framework in GPS. This role offers an opportunity to influence quality standards across a global organisation.