Dein persönlicher KI-Karriere-Agent
.Product Steward(m/w/x)
Ensuring end-to-end process knowledge for pharmaceutical manufacturing, using statistical data trending for continuous improvement. Master’s degree in Chemical Engineering or related field required. On-site work, 5-person team.
Anforderungen
- Master’s degree in Chemical Engineering, Chemistry or related scientific field
- Minimum 3 years experience in drug substance manufacturing or process support
- Knowledge of Good Manufacturing Practice and regulatory requirements
- Solid understanding of manufacturing processes, process validation and change control
- Experience with data analysis, applied statistics, and interpretation of process data
- Proven ability to work across functions and collaborate with diverse teams
- Proficiency in German and English (written and spoken)
- Experience in oligonucleotide manufacturing or development
- Applied Statistics
- Change Control
- Data Analytics and Digital
- GDP Knowledge
- gmp knowledge
- HSE Knowledge
- Manufacturing Process
- Manufacturing Production
- Manufacturing Technologies
- Operational Excellence
- Process and Cleaning Validation
- Process Control
- Quality Compliance
- Regulatory Compliance
- Resilience and Risk Management
- Technical Leadership
- Technology Transfer
Aufgaben
- Drive pharmaceutical manufacturing process performance and reliability
- Ensure end-to-end process knowledge across the product lifecycle
- Monitor process performance using statistical data trending
- Analyze critical variables to ensure process compliance
- Maintain products in a validated state through process verification
- Lead root cause investigations and implement corrective actions
- Support preventive actions and continuous process improvement
- Evaluate product performance and identify risks
- Initiate and lead optimization projects
- Collaborate cross-functionally for effective knowledge sharing
- Assess technical changes and define validation scope
- Support regulatory and process compliance activities
- Provide technical expertise for new product launches
- Author supporting documentation for new product phases
- Support product transfers with appropriate documentation
- Assist receiving sites during product transfers
Berufserfahrung
- 3 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- Good Manufacturing Practice
- Applied Statistics
- Data Analysis
- Process Validation
- Change Control
- Oligonucleotide Manufacturing
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.Product Steward(m/w/x)
Ensuring end-to-end process knowledge for pharmaceutical manufacturing, using statistical data trending for continuous improvement. Master’s degree in Chemical Engineering or related field required. On-site work, 5-person team.
Anforderungen
- Master’s degree in Chemical Engineering, Chemistry or related scientific field
- Minimum 3 years experience in drug substance manufacturing or process support
- Knowledge of Good Manufacturing Practice and regulatory requirements
- Solid understanding of manufacturing processes, process validation and change control
- Experience with data analysis, applied statistics, and interpretation of process data
- Proven ability to work across functions and collaborate with diverse teams
- Proficiency in German and English (written and spoken)
- Experience in oligonucleotide manufacturing or development
- Applied Statistics
- Change Control
- Data Analytics and Digital
- GDP Knowledge
- gmp knowledge
- HSE Knowledge
- Manufacturing Process
- Manufacturing Production
- Manufacturing Technologies
- Operational Excellence
- Process and Cleaning Validation
- Process Control
- Quality Compliance
- Regulatory Compliance
- Resilience and Risk Management
- Technical Leadership
- Technology Transfer
Aufgaben
- Drive pharmaceutical manufacturing process performance and reliability
- Ensure end-to-end process knowledge across the product lifecycle
- Monitor process performance using statistical data trending
- Analyze critical variables to ensure process compliance
- Maintain products in a validated state through process verification
- Lead root cause investigations and implement corrective actions
- Support preventive actions and continuous process improvement
- Evaluate product performance and identify risks
- Initiate and lead optimization projects
- Collaborate cross-functionally for effective knowledge sharing
- Assess technical changes and define validation scope
- Support regulatory and process compliance activities
- Provide technical expertise for new product launches
- Author supporting documentation for new product phases
- Support product transfers with appropriate documentation
- Assist receiving sites during product transfers
Berufserfahrung
- 3 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- Good Manufacturing Practice
- Applied Statistics
- Data Analysis
- Process Validation
- Change Control
- Oligonucleotide Manufacturing
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Novartis Pharma Schweizerhalle AG
Branche
Pharmaceuticals
Beschreibung
The company is committed to helping people with disease and their families through innovative science and a supportive community.
Noch nicht perfekt?
- Roche
Global MSAT Senior Product & Process Steward(m/w/x)
Vollzeitnur vor OrtSeniorBasel - 1201 F. Hoffmann-La Roche AG
Senior DP (Drug Product) Product Steward - Global MSAT(m/w/x)
Vollzeitnur vor OrtSeniorBasel - Roche
GMP Prozess Experte kommerzielle Pharmaproduktion(m/w/x)
Vollzeitnur vor OrtBerufserfahrenKaiseraugst - 1201 F. Hoffmann-La Roche AG
Global MSAT DS Senior Process Steward(m/w/x)
Vollzeitnur vor OrtSeniorBasel - 1201 F. Hoffmann-La Roche AG
Principal DP (Drug Product) Product Steward - Global MSAT(m/w/x)
Vollzeitnur vor OrtSeniorBasel