• Lead complex industrialization projects to enhance key manufacturing processes, reducing manual interventions and improving consistency.
• Identify and implement robotic, digital, and advanced manufacturing technologies to optimize production efficiency.
• Develop technical specifications for new equipment and oversee supplier selection and validation.
• Collaborate with cross-functional teams (R&D, Production, QA, Regulatory) to define automation strategies aligned with business objectives.
• Drive standardization and best practices in automation across production lines.

• Oversee the development, validation, and industrialization of new (automated or manual) processes for medical devices.
• Ensure a smooth transfer of solutions from pilot phase to full-scale production.
• Manage the scale-up projects, ensuring efficiency, reliability, and compliance with industry standards.

• Drive continuous improvement initiatives using automation to increase efficiency, reduce waste, and enhance process robustness.
• Implement data-driven solutions (IoT, predictive maintenance, AI-based monitoring) to improve manufacturing performance.
• Conduct root cause analysis and troubleshooting to enhance process reliability and product quality.

• Support the scaling-up of production activities through automation and digital transformation initiatives.
• Provide technical leadership and training to production teams on new automated systems.
• Ensure all automation projects comply with ISO 13485, FDA, and GMP regulatory requirements.
• Mentor and support junior engineers, fostering technical excellence within the team.
• Assist in budget planning, resource allocation, and project prioritization for automation initiatives.

• Master’s degree in mechanical, Industrial, or Manufacturing Engineering (or a related field).
• 8+ years of experience in medical device manufacturing or other highly regulated industries.
• Proven expertise in manufacturing, industrial automation, and lean manufacturing.
• Project management experience, including leading cross-functional automation projects from development to production scale-up.
• Knowledge in CAD, SolidWorks is a plus
• Strong knowledge of manufacturing data management and ERP systems.
• Deep understanding of ISO 13485, FDA regulations, and Good Manufacturing Practices (GMP).
• Excellent problem-solving, leadership, and communication skills with the ability to work in a multidisciplinary environment.
• Fluent in French & English.

BVI® is refocusing the future of vision.

As one of the fastest-growing, diversified surgical ophthalmic businesses in the world, our purpose-built portfolio of trusted brands includes: Beaver® (Knives and Blades), Visitec® (Cannulas), Malosa® (Single-Use Instruments), Vitreq® (Vitreoretinal Surgical Products) and PhysIOL® (Premium IOLs), and spans more than 90 countries.

We’ve set our sights on touching the lives of millions of patients affected by conditions such as cataracts, refractive error, glaucoma, retinal disease, and dry eye. Unburdened by legacy or bureaucracy, we have developed our strategy around a simple concept – taking pride in delivering innovative solutions for our physicians and patients, based on their needs. We trust and empower our associates to make decisions and solve problems because collaboration drives us. Valuing agility, simplicity, and transparency, we stay committed to listening to our customers, delivering for our patients, and keeping the future in focus.

Learn more at www.bvimedical.com