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Senior Manager Medical Device Program Lead(m/w/x)
Leading medical device development programs for biosimilars, defining device profiles and managing validation. 10+ years in FDA-regulated medical device development required. Central interface role across biosimilars project teams.
Requirements
- Bachelor’s degree or equivalent in Product design, Mechanical, Process, Materials Science or Electronic Engineering
- 5+ years of experience in project management
- 10+ years of experience in device development with understanding of device safety and regulatory requirements
- Deep technical understanding of device design, validation, verification and their link to drug development activities
- Experience in FDA regulated medical devices and combination drug device products
- Track record of resolving issues in a matrix organization
- Strong interpersonal and relationship building skills
- Solid organizational skills including attention to detail and multi-tasking skills
- Effective verbal and written communication
- Fluency in English; additional languages (German or French) are an asset
Tasks
- Lead cross-functional exercises to define targeted device profiles
- Develop project plans and budgets with internal and external teams
- Deliver quality products and processes with proper validation and regulatory documentation
- Report and control device development timelines, budgets, and risks
- Act as the main interface between biosimilars project teams and subteams
- Provide technical and business inputs to projects
- Analyze risks and suggest mitigation plans
- Oversee device development, manufacturing, validation, and regulatory activities
- Proactively identify risk areas and alert stakeholders
- Report and escalate potential issues to management
- Identify new device opportunities
- Lead innovation and continuous improvement projects
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
- French – Basic
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Senior Manager Medical Device Program Lead(m/w/x)
Leading medical device development programs for biosimilars, defining device profiles and managing validation. 10+ years in FDA-regulated medical device development required. Central interface role across biosimilars project teams.
Requirements
- Bachelor’s degree or equivalent in Product design, Mechanical, Process, Materials Science or Electronic Engineering
- 5+ years of experience in project management
- 10+ years of experience in device development with understanding of device safety and regulatory requirements
- Deep technical understanding of device design, validation, verification and their link to drug development activities
- Experience in FDA regulated medical devices and combination drug device products
- Track record of resolving issues in a matrix organization
- Strong interpersonal and relationship building skills
- Solid organizational skills including attention to detail and multi-tasking skills
- Effective verbal and written communication
- Fluency in English; additional languages (German or French) are an asset
Tasks
- Lead cross-functional exercises to define targeted device profiles
- Develop project plans and budgets with internal and external teams
- Deliver quality products and processes with proper validation and regulatory documentation
- Report and control device development timelines, budgets, and risks
- Act as the main interface between biosimilars project teams and subteams
- Provide technical and business inputs to projects
- Analyze risks and suggest mitigation plans
- Oversee device development, manufacturing, validation, and regulatory activities
- Proactively identify risk areas and alert stakeholders
- Report and escalate potential issues to management
- Identify new device opportunities
- Lead innovation and continuous improvement projects
Work Experience
- 10 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
- French – Basic
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
206030 Fresenius Kabi SwissBioSim GmbH
Industry
Pharmaceuticals
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