Regulatory Content Writer: Automate & Elevate Pharma Docs

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

Benefits offered by this job

Incentives and benefits

Career development opportunities

Job summary

Novo Nordisk is seeking a Regulatory Content Writer in Søborg, Denmark. You will drive automated authoring for regulatory documents using NovoScribe, plan content timelines, and ensure coherence, precision, and scientific rigour across documents. You will maintain the text library and push process improvements while staying updated on regulatory topics.

The role emphasizes collaboration with cross-functional teams and continuous development within a global healthcare company.

Qualifications

• MSc in Life Sciences, Pharmacy, Biology, Biochemistry, Medicine or related field.
• Excellent written English with ability to convey complex scientific information clearly.
• Ability to improve processes and promote better practices.
• Strong stakeholder management, collaboration and project coordination skills.
• Analytical, detail-oriented, curious and proactive.
• Willingness to challenge established ways and contribute to continuous improvement.

Responsibilities

• Drive development of regulatory documents following guidelines and SOPs.
• Plan content creation and set timelines for production and review.
• Evaluate documents for coherence, precision, scientific rigour and messaging.
• Maintain and expand the text library and contribute to database improvements.
• Improve best practices and innovate working methods.
• Keep updated on regulatory, scientific and medical topics relevant to drug development.

Education

MSc degree in Life Sciences or related scientific discipline

Excellent written English

Process improvement mindset

Stakeholder management & coordination

Analytical rigor and attention to detail

Proactive mindset and adaptability

Tools

NovoScribe

Job description

Novo Nordisk is seeking a Regulatory Content Writer in Søborg, Denmark. You will drive automated authoring for regulatory documents using NovoScribe, plan content timelines, and ensure coherence, precision, and scientific rigour across documents. You will maintain the text library and push process improvements while staying updated on regulatory topics.

The role emphasizes collaboration with cross-functional teams and continuous development within a global healthcare company.