R&D Technical Leader

Nouvelle opportunite : R&D Technical Leader chez Michael Page (CH).

Our client is seeking an experienced R&D Technical Leader to lead sustaining engineering activities and product lifecycle management initiatives for a portfolio of innovative healthcare products. This position plays a critical role in driving engineering changes, continuous improvement projects, and technical execution while ensuring product quality, compliance, and continuity of supply.
R&D Technical Leader
Our client is a global leader in the life sciences sector, providing innovative solutions that support the development and manufacture of critical therapies. With a strong culture of innovation and quality, the company operates in a highly regulated environment serving customers worldwide.
Description
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Lead sustaining engineering activities and product lifecycle initiatives for the disposable kits portfolio.
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Manage engineering changes, including impact assessments, risk evaluations, and stakeholder alignment.
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Drive implementation of product, material, supplier, and process changes.
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Support lifecycle management activities such as obsolescence management and component substitutions.
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Coordinate verification activities required to support product modifications.
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Conduct risk assessments and contribute to root cause investigations.
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Resolve technical, quality, and manufacturing issues through cross-functional collaboration.
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Maintain technical documentation in accordance with quality system and design control requirements.
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Partner with Manufacturing, Quality, Regulatory Affairs, Supply Chain, and suppliers to ensure successful project execution.
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Support CAPAs, non-conformance investigations, audits, and quality-related activities.
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Identify risks proactively and drive mitigation plans to ensure project delivery.
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Contribute to continuous improvement initiatives across products and processes.
Profile
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Academic degree in Mechanical Engineering, Biomedical Engineering, Materials Science, Plastics Engineering, or a related technical field.
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6 years of experience in sustaining engineering, product development, manufacturing engineering, or product lifecycle management.
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Proven parcours professionnel managing engineering changes and technical documentation within a regulated environment.
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Good understanding of medical device and/or biopharmaceutical industry requirements.
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Knowledge of Design Control principles and ISO 13485 standards.
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Experience with single-use technologies, disposable systems, plastics, or tubing assemblies is highly desirable.
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Familiarity with manufacturing processes such as assembly, injection molding, extrusion, or sterilization technologies.
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Working knowledge of risk management, root cause analysis, and product verification activities.
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Ability to independently lead technical activities and coordinate multiple stakeholders.
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Strong analytical and problem-solving capabilities.
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Excellent communication skills and ability to collaborate across international teams.
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Fluent in English; French is considered a strong asset.
Job Offer
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Exciting temporary opportunity within a leading life sciences organization.
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Exposure to innovative technologies and complex engineering challenges.
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Collaborative international environment with strong cross-functional interaction.

N'attendez pas -- envoyez votre candidature a Michael Page aujourd'hui.