Director Medical Device Program Lead
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Before you apply
LocationEysins; Spain (Remote); Madrid
Work moderemote · Switzerland
Typefull-time
SeniorityDirector
Experience5+ yrs
Company size10,000+ people
PostedNov 3, 2026 · 3d ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
Bachelor's degree (or equivalent) in an applicable Product design, Mechanical, Process, Materials Science or Electronic Engineering field
5+ years of experience in project management
10+ years of experience in device development with an understanding of device safety, regulatory requirements, policies and procedures
Experience in FDA regulated medical devices, Standalone CE marked devices and combination drug device products
Deep technical understanding of device design, validation, verification and their link to other drug development activities
Track record of resolving issues in a matrix organization
Strong interpersonal and relationship building skills with the ability to establish a trusted role with the various stakeholders
Solid organizational skills including attention to detail and multi-tasking skills
Effective verbal and written communication. Fluent in English, both oral and written
Additional languages (German or French) are an asset
About the role
Job Summary
In this position, you will be the back-up of the head of the device team.
You will be in charge of proposing some transversal activities to support innovation, strategic partnership and/or continuous improvement.
Processes.Responsibilities / Duties:
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Lead cross-functional exercises to define targeted device profiles.
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Develop device development project plans and budget with internal and external cross functional teams.
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Deliver quality products and processes with appropriate validation and regulatory documentation.
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Deliver products DHFs in compliance with defined regulation (e.g. FDA 21 CFR par 820 and part 4, ISO 13485, EMA, NbO…)
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In collaboration with Regulatory Team, write submission dossier for FDA and NbO (EMA) at first. Part of the rapid response team for all device related Health Authority IRs and requirements.
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Report and tightly control device development timelines, budget and risks to biosimilars project development team, escalate to management potential issues as needed.
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Act as the main interface between the biosimilars project development teams and the medical devices sub teams (e.g. HFE, RM, Production Unit, etc.) as well as device vendors.
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Provide technical and business inputs to projects. Analyze risks and suggest mitigation plans.
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Oversee device development, manufacturing, validation and regulatory activities.
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Proactively anticipate and identify risk areas and alert stakeholders appropriately.
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Identify new device opportunities.
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Lead innovation and/or Continuous improvement projects
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Support marketed products life cycle management activities such as complaints investigation, change controls activities and DHF update.
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Support labeling development with HFE, Regulatory and Marketing to ensure labels are available for HFE validation activities.
Technical skills:
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Deep technical understanding of device design, validation, verification and their link to other drug development activities (drug CMC, clinical, manufacturing, regulatory, quality, commercial, etc.) in the overall drug development plan.
•
Track record of resolving issues in a matrix organization.
•
Strong interpersonal and relationship building skills with the ability to establish a trusted role with the various stakeholders.
•
Solid organizational skills including attention to detail and multi-tasking skills.
•
Effective verbal and written communication. Fluent in English, both oral and written; additional languages (German or French) are an asset.
Qualification and Experience Requirements:
•
Bachelor’s degree (or equivalent) in an applicable Product design, Mechanical, Process, Materials Science or Electronic Engineering field.
•
5+ years of experience in project management
•
10+ years of experience in device development with an understanding of device safety, regulatory requirements, policies and procedures.
•
Experience in FDA regulated medical devices, Standalone CE marked devices and combination drug device products.