Senior MSAT Scientist

Novo Nordisk

Senior MSAT Scientist supporting commercial pharmaceutical manufacturing at Novo Nordisk. Collaborating with teams to ensure product quality and compliance throughout the product lifecycle.

Posted 7/22/2026full-timeHøje-Taastrup • 🇩🇰 DenmarkSenior💰 DKK 651,000 - DKK 956,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in product stability studies, regulatory submissions, and technical documentation within a GMP-regulated environment. Strong ability to analyze scientific data, mentor colleagues, and improve product quality through effective collaboration.

Highest-signal resume keywords

Product Stability StudiesGMP-Regulated EnvironmentTechnical WritingRoot Cause AnalysisScientific Problem-Solving

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Scientific Data InterpretationTechnical Documentation DevelopmentRoot Cause AnalysisQuality Issue InvestigationRegulatory Submission Support

Soft Skills

Excellent Communication SkillsCollaborationMentoring

Industry Keywords

Pharmaceutical SciencesBiotechnologyChemical EngineeringGMPHealth Authorities

About the role

Key responsibilities & impact

Lead product stability studies and interpret scientific data throughout the product lifecycle.
Monitor product stability trends and investigate out-of-trend or unexpected results.
Provide scientific product quality support to Manufacturing during deviations and investigations.
Perform root cause analysis and recommend scientifically sound solutions.
Support regulatory submissions and lifecycle management activities.
Develop and review technical documentation, protocols and scientific reports.
Work closely with Manufacturing, QC, QA and CMC to resolve complex technical issues.
Contribute to regulatory inspections and interactions with Health Authorities.
Mentor junior colleagues and share scientific knowledge across the team.
Identify opportunities to improve processes, product quality and ways of working.

Requirements

What you’ll need

Bachelor's or Master's degree (or equivalent) in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, Chemical Engineering or another relevant scientific discipline.
Experience working within a GMP-regulated pharmaceutical, biotechnology or other highly regulated manufacturing environment.
Strong scientific problem-solving skills.
Experience investigating technical or quality-related issues.
Excellent written and verbal communication skills in English.
Strong technical writing and documentation skills.
Ability to work independently while collaborating effectively with multiple stakeholders.

Benefits

Comp & perks

short- and/or long-term incentives
additional employee benefits