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Assoc. Director, Quality Management, Contract Manufacturing(m/w/x)
Description
As an Associate Director of Quality Management, you will lead a quality team focused on contract manufacturing, ensuring compliance and driving continuous improvement while collaborating with various departments to enhance supplier capabilities.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Valid Swiss work visa or existing work authorization
- •10 years of senior experience in regulated industries
- •Strong leadership, project management, and cross-regional coordination skills
- •Bachelor’s degree in a technical field; Master’s degree a plus
- •10+ years of experience in electromechanical instrumentation manufacturing
- •Strong QMS expertise; product design, manufacturing, supply chain knowledge; ideally electromechanical
- •Deep knowledge of ISO 13485, FDA QSR, ISO 14971, and international medical device regulations
- •Strong leadership, project management, and cross-regional coordination skills
- •Ability to influence stakeholders and drive results in complex environments
Education
Work Experience
10 years
Tasks
- •Lead and develop a dedicated Contract Manufacturing Quality team
- •Drive supplier qualification, audits, and performance management
- •Champion continuous improvement using Lean, Six Sigma, and advanced quality methodologies
- •Partner with design, manufacturing, supply chain, and procurement leaders to resolve challenges and enhance supplier capabilities
- •Represent the organization during FDA and notified body inspections
- •Report key metrics and trends to senior leadership, shaping long-term strategy
Languages
English – Business Fluent
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Assoc. Director, Quality Management, Contract Manufacturing(m/w/x)
The AI Job Search Engine
Description
As an Associate Director of Quality Management, you will lead a quality team focused on contract manufacturing, ensuring compliance and driving continuous improvement while collaborating with various departments to enhance supplier capabilities.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Valid Swiss work visa or existing work authorization
- •10 years of senior experience in regulated industries
- •Strong leadership, project management, and cross-regional coordination skills
- •Bachelor’s degree in a technical field; Master’s degree a plus
- •10+ years of experience in electromechanical instrumentation manufacturing
- •Strong QMS expertise; product design, manufacturing, supply chain knowledge; ideally electromechanical
- •Deep knowledge of ISO 13485, FDA QSR, ISO 14971, and international medical device regulations
- •Strong leadership, project management, and cross-regional coordination skills
- •Ability to influence stakeholders and drive results in complex environments
Education
Work Experience
10 years
Tasks
- •Lead and develop a dedicated Contract Manufacturing Quality team
- •Drive supplier qualification, audits, and performance management
- •Champion continuous improvement using Lean, Six Sigma, and advanced quality methodologies
- •Partner with design, manufacturing, supply chain, and procurement leaders to resolve challenges and enhance supplier capabilities
- •Represent the organization during FDA and notified body inspections
- •Report key metrics and trends to senior leadership, shaping long-term strategy
Languages
English – Business Fluent
About the Company
Becton, Dickinson and Company
Industry
Healthcare
Description
The company is a global leader in medical technology, advancing health through innovation in medical discovery, diagnostics, and care delivery.
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