Development Scientist

Novo Nordisk

. Design and manage stability studies, including preparation of protocols, reports, and regulatory documentation .

Posted 9/22/2026full-timeBagsværd • DenmarkMid-LevelSenior💰 DKK 651,000 - DKK 956,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in designing and managing stability studies, including regulatory documentation and data analysis, while effectively communicating scientific recommendations. Proven ability to drive continuous improvement initiatives and optimize processes within a GMP-regulated pharmaceutical environment.

Highest-signal resume keywords

MSc Or PhD In Pharmacy, Biochemistry, Chemical Engineering5+ Years Experience In Pharmaceutical IndustryStability Studies ManagementGMP-Regulated Environment ExperienceRegulatory Documentation Contribution

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Stability Data AnalysisProtocol PreparationReport WritingRegulatory SubmissionProcess Optimization

Soft Skills

Strong Communication SkillsAbility To Manage Multiple PrioritiesOwnership

Industry Keywords

Stability StudiesGMP CompliancePharmaceutical IndustryLife-Cycle ManagementHealth Authority Engagement

About the role

Key responsibilities & impact

Design and manage stability studies, including preparation of protocols, reports, and regulatory documentation
Analyse stability data, identify trends, and provide scientific recommendations to support decision-making
Support production and integrate stability considerations into manufacturing activities
Contribute to investigations, deviations, and regulatory submissions related to stability
Drive continuous improvement initiatives and identify opportunities to optimise processes
Assess the necessity and evaluate the outcomes of stability studies
Support stability activities for life-cycle management products and products transitioning from development to production

Requirements

What you’ll need

An MSc degree or higher (for example a PhD) within Pharmacy, Biochemistry, Chemical Engineering, or another relevant scientific discipline with expertise in stability
Minimum 5 years of relevant experience within the pharmaceutical industry
Experience working in a GMP-regulated environment
Previous experience with stability studies, stability data evaluation, or related scientific activities
Strong communication skills
Professional proficiency in English
Danish language skills are an advantage but not a requirement
Ability to identify opportunities, drive optimisation initiatives, and deliver results
Experience engaging with health authorities and contributing to regulatory documentation is an advantage
Ability to manage multiple priorities and take ownership

Benefits

Comp & perks

Short-term and/or long-term incentives
Other employee benefits based on position level, location, functional area and relevant market benchmarks
Opportunities to learn and develop
Collaboration, knowledge sharing, and continuous development