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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
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Ergonomic Workplace
- Workplace accommodation
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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
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Ergonomic Workplace
- Workplace accommodation
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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?
- Lilly Deutschland GmbH
Sterility Assurance Advisor – Technical Services/Manufacturing Science (TS/MS)(m/w/x)
Full-timeOn-siteSeniorAlzey - 350 Lilly Deutschland GmbH
Sterility Assurance Advisor- Technical Services/Manufacturing Science (TS/MS)(m/w/x)
Full-timeOn-siteSeniorAlzey - 350 Lilly Deutschland GmbH
Scientist – TSMS Device Assembly and Packaging(m/w/x)
Full-timeOn-siteSeniorAlzey - Lilly
Senior Principal Scientist – Sterility Assurance - Technical Services/Manufacturing Science(m/w/x)
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