GLP QA Specialist — Non-Clinical Quality Assurance

Novo Nordisk A/S; Søborg; Remote; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk A/S in Søborg seeks a GLP QA Professional to ensure GLP standards in non-clinical research. You will oversee studies, evaluate internal and external work, and translate findings into practical quality recommendations that keep research reliable and moving forward.

You will partner with CROs and internal teams to maintain the QMS, lead inspections, and support audits while communicating clearly in English. Some travel may be required for audits and GLP activities.

Qualifications

• Experience as a laboratory technician and relevant qualification, or a master’s degree in science, pharmacy, medicine or a similar field.
• Experience within GLP, for example from quality assurance, GLP-regulated work, non-clinical research or laboratory activities.
• Knowledge of Quality Management Systems (QMS) and the ability to interpret and communicate regulatory and procedural requirements.
• Strong analytical and organisational skills, with attention to detail and the ability to work systematically and independently.
• Strong collaboration and stakeholder management skills, including the ability to build constructive relationships with internal colleagues and external Contract Research Organisations (CROs).
• Proficiency in written and spoken English, and confidence in communicating observations, recommendations and quality matters.

Responsibilities

• Perform quality oversight and compliance verification of GLP-regulated activities, including review of study plans, reports, relevant SOPs and documentation from internal areas and external CROs.
• Plan and conduct study-based and process-based internal inspections, including Good Clinical Laboratory Practice (GCLP) activities where relevant.
• Support stakeholders on GLP requirements and general quality matters, including review of GLP action plans from internal and external audits.
• Contribute to maintaining and improving the department’s QMS, including harmonisation, digitalisation and simplification initiatives.
• Communicate observations, regulatory requirements and practical quality recommendations clearly to internal and external stakeholders, and take part in relevant projects, audits and regulatory inspections.

Skills

Quality mindset

Analytical skills

Organisational skills

English proficiency

Stakeholder management

Independent worker

Education

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

Laboratory technician experience or relevant qualification

Job description

Novo Nordisk A/S in Søborg seeks a GLP QA Professional to ensure GLP standards in non-clinical research. You will oversee studies, evaluate internal and external work, and translate findings into practical quality recommendations that keep research reliable and moving forward.

You will partner with CROs and internal teams to maintain the QMS, lead inspections, and support audits while communicating clearly in English. Some travel may be required for audits and GLP activities.