The Project Manager is responsible for managing customer projects related to medical device transfer and industrialization activities from initial handover through successful implementation into manufacturing.

The role acts as the primary interface between the customer and internal teams, ensuring project execution according to quality, timeline, regulatory, and cost objectives. The Project Manager also drives continuous process improvement initiatives to enhance manufacturing efficiency, quality, and customer satisfaction.

Project Management & Customer Interface

• Lead project transfer activities from customer sites to internal manufacturing operations.
• Define project scope, timelines, milestones, risks, and deliverables.
• Organize and lead project meetings with customers and cross-functional internal teams.
• Ensure projects are delivered on time, within budget, and according to quality requirements.

Industrialization & Process Transfer

• Coordinate manufacturing transfer and process validation activities.
• Collaborate with Engineering, Quality, Production, Supply Chain, and Regulatory teams to ensure smooth project implementation.
• Support development and optimization of manufacturing processes and work instructions.

Continuous Improvement

• Identify opportunities for process improvement, cost reduction, and operational efficiency.
• Implement corrective and preventive actions when required.

Quality & Regulatory Compliance

• Ensure compliance with applicable medical device regulations and quality system requirements.
• Support risk management, deviation management, and change control activities.
• Participate in audits and customer visits when required.

• Engineering degree (Mechanical, Industrial, Biomedical, Manufacturing, or related field).
• Minimum 5 years of experience in project management within the MedTech or medical device manufacturing industry.
• Experience in contract manufacturing or industrial project transfer is strongly preferred.
• Good understanding of medical device manufacturing processes and quality requirements.
• Experience working in a regulated environment (ISO 13485, GMP, FDA requirements) is an advantage.
• Strong organizational and problem-solving skills.
• Ability to manage multiple projects simultaneously.
• Excellent communication and customer relationship management skills.