Process Scientist – Analytical QC Equipment & Methods

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

Job summary

Novo Nordisk in Kalundborg is seeking a Process Scientist to support Specialized QC Utility, bridging analytical equipment management and analytical technology to ensure qualified, reliable tools for quality control and production.

You will qualify equipment (NIR, PSD, Karl Fischer, pH meters, balances, pipettes), support method development and validation, troubleshoot issues, manage lifecycle and SOP changes in GMP, and help implement new technologies across production.

Qualifications

• Relevant academic degree in chemistry, pharmaceutical sciences, chemical engineering or related discipline.
• GMP experience in a QA/QC environment and analytical lab experience.
• Experience with method development, validation and data evaluation.
• Familiarity with change control, deviation handling and SOP management.

Responsibilities

• Qualify and implement new analytical equipment (NIR, PSD, Karl Fischer, pH meters, balances, pipettes).
• Collaborate with process development and manufacturing development on methods from study design to reporting.
• Troubleshoot equipment-related issues and provide hands-on lab support.
• Conduct life-cycle management activities and assess performance trends.
• Manage change requests, deviations and SOP updates to GMP standards.
• Contribute to implementing new technologies across production areas.

Skills

GMP experience

QC instrumentation

IT literacy

Analytical data analysis

Communication

Teamwork

Education

Chemistry degree

Pharmaceutical sciences degree

Chemical engineering degree

Tools

LIMS

TIMS

Job description

Novo Nordisk in Kalundborg is seeking a Process Scientist to support Specialized QC Utility, bridging analytical equipment management and analytical technology to ensure qualified, reliable tools for quality control and production.

You will qualify equipment (NIR, PSD, Karl Fischer, pH meters, balances, pipettes), support method development and validation, troubleshoot issues, manage lifecycle and SOP changes in GMP, and help implement new technologies across production.