GLP QA Specialist: Non-Clinical Quality & Compliance

Novo Nordisk; Gladsaxe Kommune; On-site; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk in Søborg, Denmark, is seeking a GLP QA Professional to ensure non-clinical research meets GLP standards. You will oversee studies, review internal and external work, and translate findings into practical quality recommendations.

You will join Non-Clinical Quality, a 15-person team, and collaborate across CROs and internal partners to strengthen the QMS and drive compliant, reliable research processes.

Qualifications

• Experience in GLP, quality assurance or non-clinical research.
• Ability to interpret regulatory and procedural requirements.
• Strong analytical and organisational skills with attention to detail.
• Excellent written and spoken English.

Responsibilities

• Quality oversight and compliance verification of GLP-regulated activities.
• Plan and conduct internal inspections, including GCLP where relevant.
• Support stakeholders on GLP requirements and audit findings.
• Contribute to maintaining and improving the QMS.
• Communicate observations and recommendations clearly to stakeholders.

Skills

Quality mindset

Analytical skills

Independent worker

Stakeholder management

English communication

Education

Master’s degree in science, pharmacy, medicine or similar

Experience as a laboratory technician

Tools

QMS knowledge

Job description

Novo Nordisk in Søborg, Denmark, is seeking a GLP QA Professional to ensure non-clinical research meets GLP standards. You will oversee studies, review internal and external work, and translate findings into practical quality recommendations.

You will join Non-Clinical Quality, a 15-person team, and collaborate across CROs and internal partners to strengthen the QMS and drive compliant, reliable research processes.