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Site Molecule Steward(m/w/x)
Technical leadership for parenteral drug product manufacturing, implementing site control strategies at a global healthcare leader. Bachelor's degree in science or engineering and parenteral product manufacturing experience required. Workplace accommodation provided.
Requirements
- Bachelor's degree in science or engineering
- Experience supporting parenteral product manufacturing
- Strong communication skills
- Ability to prioritize and multi-task
- Collaboration with cross-functional teams
Tasks
- Act as the technical subject matter expert for drug product manufacturing
- Provide technical leadership for TS/MS projects
- Own the implementation of site control strategies
- Collaborate with parenteral network peers in QA, QC, and Engineering
- Coordinate regularly with drug substance counterparts
- Align technical strategies with quality and regulatory guidance
- Investigate product performance with a curious and analytical mindset
- Coach site staff to build technical capabilities
- Direct responses to deviations and production challenges
- Assess the impact of manufacturing change controls
- Represent the TS/MS function during regulatory interactions
- Monitor and implement external corporate technical trends
- Transfer technical knowledge across all organizational levels
- Influence cross-functional teams to meet business objectives
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Ergonomic Workplace
- Workplace accommodation
Not a perfect match?
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Site Molecule Steward(m/w/x)
Technical leadership for parenteral drug product manufacturing, implementing site control strategies at a global healthcare leader. Bachelor's degree in science or engineering and parenteral product manufacturing experience required. Workplace accommodation provided.
Requirements
- Bachelor's degree in science or engineering
- Experience supporting parenteral product manufacturing
- Strong communication skills
- Ability to prioritize and multi-task
- Collaboration with cross-functional teams
Tasks
- Act as the technical subject matter expert for drug product manufacturing
- Provide technical leadership for TS/MS projects
- Own the implementation of site control strategies
- Collaborate with parenteral network peers in QA, QC, and Engineering
- Coordinate regularly with drug substance counterparts
- Align technical strategies with quality and regulatory guidance
- Investigate product performance with a curious and analytical mindset
- Coach site staff to build technical capabilities
- Direct responses to deviations and production challenges
- Assess the impact of manufacturing change controls
- Represent the TS/MS function during regulatory interactions
- Monitor and implement external corporate technical trends
- Transfer technical knowledge across all organizational levels
- Influence cross-functional teams to meet business objectives
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Ergonomic Workplace
- Workplace accommodation
About the Company
Lilly Deutschland GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer im Gesundheitswesen mit Fokus auf die Entwicklung lebensverändernder Medikamente.
Not a perfect match?
- 350 Lilly Deutschland GmbH
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Scientist – TSMS Device Assembly and Packaging(m/w/x)
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Full-timeOn-siteSeniorAlzey - 350 Lilly Deutschland GmbH
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