Manufacturing Engineer

Our client, a well-established med tech company in Geneva, is seeking an experienced Manufacturing Engineer for a six-month contract. The successful candidate will support product design transfer to manufacturing and manage equipment qualification and validation.
This is a hands-on role requiring on-site presence to guarantee smooth production processes and compliance in a high-regulation environment.

Key Responsibilities:

• Design Transfer: Manage and facilitate the smooth transition of product designs from the development phase into manufacturing.
• Equipment Management: Review, maintain, and update procedures related to the maintenance and calibration of manufacturing equipment.
• Compliance Management: Handle change requests in compliance with FDA regulations, ensuring all processes meet stringent regulatory standards.
• CAPA & Deviation Management: Identify, investigate, and manage Corrective and Preventive Actions (CAPA) and deviations to maintain high-quality standards and resolve any issues in manufacturing processes.
• Equipment qualification and validation: Ensure compliant Qualification and validation of manufacturing equipments.

Profile:

• Education: Bachelor's degree in Engineering or a related technical field.
• Experience: Proven experience in the medical technology sector, with a focus on FDA compliance, CAPA, and deviation management.
• Good knowledge of all the equipment Qualification processes
• French and English fluent, written and spoken