The Engineer Shall:

• Contribute to the development of the product by optimizing product design, related accessories, and packaging
• Support in establishing design specification and development of clinically relevant test methodology that would meet the specifications
• Take responsibility for the production and assembly of prototypes, tooling and test equipment
• Liaise and manage subcontractors, planning, implementing, monitoring and controlling product development processes
• Maintain AutoCAD models, drawings and other technical documentation according to ISO 13485 regulations and company procedures Ad-hoc tasks
• Support in other ad-hoc activities

Requirements:

• Bachelor’s degree in mechanical/biomedical engineering, or related technical degree
• Experience in design, AutoCAD (Solidworks) and technical drawings
• Product development experiences in medical products
• Minimum of 2 years experiences in a manufacturing environment (i.e: Product development/production/manufacturing)
• Knowledge of in IQPQ, validation, validation processes for medical devices is an advantage
• Knowledge of regulatory processes will be an added advantage
• Knowledge to solve technical problems and has a creative approach to problem solving
• Good verbal and written command of English

Skills:

• Attention to details and is highly analytical
• Keen to troubleshoot and is creative and innovative in problem solving
• Comfortable working independently or as a team
• Proactive