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Assoc. Dir., Engineering(m/w/x)
Technical interface for ADC drug substance manufacturing and tech transfers within an external partner network. Minimum 5 years of bioconjugation or ADC DS manufacturing experience required. Flexible hybrid work model with 30 days vacation.
Requirements
- Understanding of regulatory requirements and partnerships
- 10 years manufacturing experience
- 5 years Bioconjugation/ADC DS manufacturing experience
- Experience leading technical transfers and manufacturing
- Proven people management and coaching experience
- Authentic and inclusive people leadership
- Ability to build collaborative internal relations
- Strong professional and interpersonal communication skills
- Ability to multi-task under deadlines
- Flexibility, independence, and organizational skills
- Knowledge of Bioconjugation Chemistry and Validation
- Analytical problem-solving and risk assessment skills
- Excellent command of English
- Lean Manufacturing or Six Sigma experience
- Project management experience
- Knowledge of worldwide regulatory requirements
- Italian and/or German language skills
- Expertise in Automation Systems and Scale-Up
Tasks
- Act as the primary technical interface with external partners
- Lead tech transfers and commercial manufacturing for ADC drug substance
- Manage a high-performing team of technical operations engineers
- Provide technical guidance and verify standards for external partners
- Assess technology viability in proposed process configurations
- Identify partner risks and develop mitigation plans
- Evaluate external partners for network inclusion with cross-functional teams
- Execute technical due diligence assessments at partner sites
- Execute validation strategies for new and existing products
- Resolve production issues and optimize process capacity
- Manage complex investigations across impacted manufacturing sites
- Review partner process changes, deviations, and master batch records
- Minimize effort duplication between partner and internal systems
- Drive continuous process verification and performance monitoring
- Develop efficient ways to meet regulatory requirements with partners
Work Experience
Education
Languages
Tools & Technologies
Benefits
Flexible Working
- •Hybrid work arrangement
- •Flexible work arrangements
- MSD Animal Health GmbHFull-timeOn-siteManagementfrom 82,400 / yearLuzern
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Assoc. Dir., Engineering(m/w/x)
Technical interface for ADC drug substance manufacturing and tech transfers within an external partner network. Minimum 5 years of bioconjugation or ADC DS manufacturing experience required. Flexible hybrid work model with 30 days vacation.
Requirements
- Understanding of regulatory requirements and partnerships
- 10 years manufacturing experience
- 5 years Bioconjugation/ADC DS manufacturing experience
- Experience leading technical transfers and manufacturing
- Proven people management and coaching experience
- Authentic and inclusive people leadership
- Ability to build collaborative internal relations
- Strong professional and interpersonal communication skills
- Ability to multi-task under deadlines
- Flexibility, independence, and organizational skills
- Knowledge of Bioconjugation Chemistry and Validation
- Analytical problem-solving and risk assessment skills
- Excellent command of English
- Lean Manufacturing or Six Sigma experience
- Project management experience
- Knowledge of worldwide regulatory requirements
- Italian and/or German language skills
- Expertise in Automation Systems and Scale-Up
Tasks
- Act as the primary technical interface with external partners
- Lead tech transfers and commercial manufacturing for ADC drug substance
- Manage a high-performing team of technical operations engineers
- Provide technical guidance and verify standards for external partners
- Assess technology viability in proposed process configurations
- Identify partner risks and develop mitigation plans
- Evaluate external partners for network inclusion with cross-functional teams
- Execute technical due diligence assessments at partner sites
- Execute validation strategies for new and existing products
- Resolve production issues and optimize process capacity
- Manage complex investigations across impacted manufacturing sites
- Review partner process changes, deviations, and master batch records
- Minimize effort duplication between partner and internal systems
- Drive continuous process verification and performance monitoring
- Develop efficient ways to meet regulatory requirements with partners
Work Experience
Education
Languages
Tools & Technologies
Benefits
Flexible Working
- •Hybrid work arrangement
- •Flexible work arrangements
About the Company
Merck & Co., Inc.
Industry
Pharmaceuticals
Description
Das Unternehmen agiert als weltweit zuverlässiger Hersteller und Lieferant von Biopharmazeutika und beliefert Kunden und Patienten mit qualitativ hochwertigen Produkten.
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