Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future
Role Overview
We are seeking a highly technical Lens Manufacturing Engineer (Injection Moulding) to join the Process Engineering team at Bausch + Lomb Ireland. This role supports, maintains, debugs, and continuously improves injection moulding systems and associated automation in a high-volume, medical device manufacturing environment. The position includes significant responsibility for engineering support and maintenance-facing activities on site injection moulding equipment
Key Responsibilities
Develop, design, and implement cost-justified process and equipment improvements with minimal impact to production in a 24/7 manufacturing environment.
Provide hands‑on technical and engineering support for site injection moulding equipment
Work closely with maintenance technicians to support moulding equipment reliability and performance.
Identify, investigate, and eliminate repetitious machine and process failures.
Carry out fault‑finding and systematic troubleshooting of equipment and process issues.
Support the installation, commissioning, and validation of automation and equipment upgrades.
Utilise Lean and Six Sigma tools and data to drive continuous improvement initiatives.
Develop and implement safety and quality improvements across moulding operations.
Prepare engineering documentation including design specifications, upgrade documentation, and functional and detailed design specifications.
Translate formal and informal User Requirement Specifications (URS) into engineering solutions
Implement process and equipment improvements under formal change controls.
Present technical data, where appropriate, to internal and external audit and inspection groups.
Ensure full compliance with Health & Safety procedures and regulatory requirements at all times.
Qualifications & Experience
Bachelor’s Degree in Engineering (Polymer, Mechanical, Electronic, or related discipline preferred.
Minimum of 3–5 years’ experience in a technical engineering role within a high-volume manufacturing environment.
Strong experience with injection moulding processes and associated automation.
Experience working in a validated environment with a strong discipline around change control.
Demonstrated problem‑solving skills with a structured, data‑driven approach.
Medical device and/or pharmaceutical manufacturing experience is strongly preferred
Lean Six Sigma experience or certification is desirable.
SolidWorks experience is advantageous.
Familiarity with 21 CFR Part 820 and regulatory audit requirements is a plus.
Key Attri
butesHands-on, solutions-focused engineer with strong troubleshooting capability.
Comfortable operating in fast-paced, high-volume manufacturing environments.
Strong communication skills and ability to work cross-functionally with maintenance, manufacturing, and quality teams.
High attention to detail, particularly in documentation and compliance.
Continuous improvement mindset with a strong focus on safety and quality.
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