Senior Method Development Scientist - Process Analytics

Healthcare Businesswomen’s Association; Schaftenau; Hybrid; EUR 61.000 - 96.000; Vollzeit

Zusammenfassung

Novartis in Schaftenau, Austria is seeking an Expert in the Method Development Team in Process Analytical Sciences (PAS) to lead physical chemical method development, optimization, and robustness testing in late-phase drug development.

The role combines laboratory development with documentation in a hybrid環vironment. It requires MSc with 2+ years in (bio)pharma or PhD with 1 year, strong analytical skills and digital proficiency.

Qualifikationen

• MSc with 2+ years in (bio)pharma industry (or PhD with 1 year).
• Experience in Analytical Development and DS/DP process development.
• Strong collaboration and communication skills.
• Proficiency in English; German beneficial.
• Proficiency with digital technologies.

Aufgaben

• Plan, perform and document physical chemical method development (e.g., HPLC/CE).
• Utilize chromatographic or statistical software to increase efficiency.
• Transfer analytical methods to internal teams and CROs.
• Collaborate with PAS labs, AE, and cross-functional teams for analytical workflows.
• Design and execute DoE-based analytical approaches for DS/DP ensuring QbD alignment.
• Interpret results and lead root cause investigations and issue resolution.
• Author reports and support regulatory submissions; participate in audits.
• Present results, contribute to publications, and support patents.
• Promote digitalization and data-driven quality improvements.

Kenntnisse

Analytical Development

Data & Digital Tools

Collaboration & teamwork

English proficiency

German beneficial

Ausbildung

MSc in pharmaceutical science or related field

Tools

HPLC

CE

DoE software

Jobbeschreibung

Novartis in Schaftenau, Austria is seeking an Expert in the Method Development Team in Process Analytical Sciences (PAS) to lead physical chemical method development, optimization, and robustness testing in late-phase drug development.

The role combines laboratory development with documentation in a hybrid環vironment. It requires MSc with 2+ years in (bio)pharma or PhD with 1 year, strong analytical skills and digital proficiency.