Description

* Lead impactful product lifecycle projects.
* Work with diverse international teams.

## About Our Client ##



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.

## Job Description ##

* Lead sustaining engineering activities and product lifecycle initiatives for the disposable kits portfolio.
* Manage engineering changes, including impact assessments, risk evaluations, and stakeholder alignment.
* Drive implementation of product, material, supplier, and process changes.
* Support lifecycle management activities such as obsolescence management and component substitutions.
* Coordinate verification activities required to support product modifications.
* Conduct risk assessments and contribute to root cause investigations.
* Resolve technical, quality, and manufacturing issues through cross-functional collaboration.
* Maintain technical documentation in accordance with quality system and design control requirements.
* Partner with Manufacturing, Quality, Regulatory Affairs, Supply Chain, and suppliers to ensure successful project execution.
* Support CAPAs, non-conformance investigations, audits, and quality-related activities.
* Identify risks proactively and drive mitigation plans to ensure project delivery.
* Contribute to continuous improvement initiatives across products and processes.





## The Successful Applicant ##

* Academic degree in Mechanical Engineering, Biomedical Engineering, Materials Science, Plastics Engineering, or a related technical field.
* 6 years of experience in sustaining engineering, product development, manufacturing engineering, or product lifecycle management.
* Proven experience managing engineering changes and technical documentation within a regulated environment.
* Good understanding of medical device and/or biopharmaceutical industry requirements.
* Knowledge of Design Control principles and ISO 13485 standards.
* Experience with single-use technologies, disposable systems, plastics, or tubing assemblies is highly desirable.
* Familiarity with manufacturing processes such as assembly, injection molding, extrusion, or sterilization technologies.
* Working knowledge of risk management, root cause analysis, and product verification activities.
* Ability to independently lead technical activities and coordinate multiple stakeholders.
* Strong analytical and problem-solving capabilities.
* Excellent communication skills and ability to collaborate across international teams.
* Fluent in English; French is considered a strong asset.





## What's on Offer ##

* Exciting temporary opportunity within a leading life sciences organization.
* Exposure to innovative technologies and complex engineering challenges.
* Collaborative international environment with strong cross-functional interaction.





Quote job ref

JN-072026-7060303

Job Function

Engineering & Manufacturing

Specialisation

Mechanical Engineering

Industry

Healthcare / Pharmaceutical

Where

Geneva

Contract Type

Interim

Job Reference

JN-072026-7060303