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Associate Director, Reliability and Product Improvement(m/w/x)
Technical leadership for marketed combination products in biotherapeutics. 10+ years in parenteral or device manufacturing required. Well-being support, team management experience.
Requirements
- Bachelor's in engineering (mechanical or chemical preferred)
- Minimum 10 years of experience in parenteral or device manufacturing in pharmaceutical space
- Leadership experience in team management or supervision
- Experience with manufacturing processes, validation practices, and cGMP guidelines
- Knowledge of process automation and equipment reliability
- Ability to collaborate with internal teams, CMs, and contractors
Tasks
- Provide technical leadership for marketed combination products
- Collaborate with DDSP and Quality Assurance for product improvements
- Implement process optimization and CDMO evaluation
- Manage tech transfers and supplier-related changes
- Update risk management practices
- Identify and standardize best practices for combination products
- Interface with project teams and external organizations
- Scope and vet design improvement projects
- Ensure compliance with ISO 13485, ISO 14971, 21 CFR Part 4, QMSR, and 211
- Follow relevant ICH guidelines
- Partner with manufacturing, CDMOs, and quality for design improvements
- Drive process optimizations and supplier changes through change control
- Represent the function in cross-functional program teams
- Participate in design reviews and regulatory interactions
- Provide expert input on device reliability for Health Authority submissions
- Support regulatory audits and inspections
- Maintain knowledge of evolving combination product regulations
- Monitor and improve the product complaint process
- Educate new product development leads on best practices
- Utilize technical project management skills
- Plan resources and work
- Manage risks and prioritize tasks
- Resolve conflicts and manage changes
- Report project progress
- Ensure safety, quality, and reliability of commercialized products
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Mental Health Support
- Well-being support
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Associate Director, Reliability and Product Improvement(m/w/x)
Technical leadership for marketed combination products in biotherapeutics. 10+ years in parenteral or device manufacturing required. Well-being support, team management experience.
Requirements
- Bachelor's in engineering (mechanical or chemical preferred)
- Minimum 10 years of experience in parenteral or device manufacturing in pharmaceutical space
- Leadership experience in team management or supervision
- Experience with manufacturing processes, validation practices, and cGMP guidelines
- Knowledge of process automation and equipment reliability
- Ability to collaborate with internal teams, CMs, and contractors
Tasks
- Provide technical leadership for marketed combination products
- Collaborate with DDSP and Quality Assurance for product improvements
- Implement process optimization and CDMO evaluation
- Manage tech transfers and supplier-related changes
- Update risk management practices
- Identify and standardize best practices for combination products
- Interface with project teams and external organizations
- Scope and vet design improvement projects
- Ensure compliance with ISO 13485, ISO 14971, 21 CFR Part 4, QMSR, and 211
- Follow relevant ICH guidelines
- Partner with manufacturing, CDMOs, and quality for design improvements
- Drive process optimizations and supplier changes through change control
- Represent the function in cross-functional program teams
- Participate in design reviews and regulatory interactions
- Provide expert input on device reliability for Health Authority submissions
- Support regulatory audits and inspections
- Maintain knowledge of evolving combination product regulations
- Monitor and improve the product complaint process
- Educate new product development leads on best practices
- Utilize technical project management skills
- Plan resources and work
- Manage risks and prioritize tasks
- Resolve conflicts and manage changes
- Report project progress
- Ensure safety, quality, and reliability of commercialized products
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Mental Health Support
- Well-being support
About the Company
CSL Behring AG (CH)
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein weltweit führendes Biotech-Unternehmen, das lebensrettende Therapien für Menschen mit schweren und seltenen Krankheiten entwickelt und vertreibt.
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