GLP QA professional

Cari; Søborg; Remote; DKK 570,000 - 838,000; Full time

Job summary

Novo in Søborg is seeking a GLP QA Professional to ensure non-clinical research meets Good Laboratory Practice standards. You will oversee studies, inspect internal and external work, and translate findings into practical recommendations that keep research reliable and moving.

You will strengthen the department’s QMS, harmonise processes, and collaborate with internal colleagues and external CROs. Some travel may be required for audits and inspections.

Qualifications

• Experience in GLP or GLP-regulated work
• Strong knowledge of QMS and regulatory requirements
• Excellent analytical and organisational skills
• Fluent in English, able to communicate findings clearly

Responsibilities

• Perform quality oversight and compliance verification of GLP-regulated activities
• Plan and conduct study-based and process-based internal inspections
• Support stakeholders on GLP requirements and action plans from audits
• Contribute to maintaining and improving the department’s QMS and digitalisation initiatives
• Communicate observations and recommendations to stakeholders

Skills

GLP knowledge

Quality management

Analytical

Organisational skills

Education

Master's degree in science/ pharmacy/ medicine

Job description

Your impact begins here. As GLP QA Professional, you will help ensure non-clinical research at Novo is carried out to Good Laboratory Practice (GLP) standards. You will oversee studies, inspect internal and external work, and turn what you see into clear, practical recommendations that keep research reliable and moving. You will shape how quality is built into non-clinical processes, strengthening the foundation for treatments for people living with serious chronic diseases.

What you’ll bring

• 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.

Desirable, but not essential:

• Experience from industrial drug development.

What you’ll do

• 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.

Who you’ll work with

You will join Non-Clinical Quality, a diverse team of 15 skilled colleagues in Søborg. It is one of two sister departments within Process Management, Non-Clinical, IT & AI Quality, part of R&D Quality. In R&D, curiosity, data, collaboration and operational excellence come together to advance scientific ideas towards clinical testing, and Non-Clinical Quality helps make sure the processes behind that work are fit for purpose.

The team provides QMS expertise to a global organisation and works closely with stakeholders across the value chain. You will have many interfaces: research and laboratory colleagues in internal areas, external CROs and other collaboration partners, and teams across the organisation working on improvement projects.

You will work in an international environment where clear communication helps you build trust, create clarity around requirements and keep work moving. Some travel may be required for audits and other GLP QA activities.

What you can expect here

You will build your GLP expertise and take on increasing responsibility, with room to influence how quality is embedded in non-clinical research processes. Alongside day-to-day oversight, you will contribute to cross-organisational improvement projects and share ideas that improve methods, systems and processes.

You will be supported to perform at your best, trusted to work independently and encouraged to make your voice heard. You will grow through practical experience, close collaboration with colleagues and continuous learning.

Salary

For this role, the Annual Base Salary ranges from 570,200.00 to 838,100.00 DKK, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate's skills, competencies, knowledge and relevant experience.

Incentives and Benefits

The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

We are an equal opportunities employer and are committed to an inclusive recruitment process and equality of opportunity for all applicants.

Learn more about our Reward Philosophy here

Deadline: 13 November 2026.