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. #J-18808-Ljbffr
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. The Regulatory Affairs Specialist is responsible for providing regulatory support across global markets. The role coordinates collaboration between local and regional teams and medical device manufacturers to ensure the timely delivery of regulatory documentation, aligned with corporate strategies, notification and submission timelines, and all applicable regulatory requirements. This position is a hybrid role based in the Dublin, City West office, with 3 days in the office and 2 days from home. Key Activities / Responsibilities Coordinate the regulatory activities related to new markets expansion and MOB implementation. Contribute to the planning and tracking of regulatory submissions across multiple regions. Maintain project timelines, trackers, and documentation to support efficient execution of regulatory activities. Collaborate with global and regional Regulatory Affairs teams to facilitate alignment on submission timelines and requirements. Monitor progress of regulatory deliverables and follow up with stakeholders to support timely completion of activities. Represent Regulatory Affairs on cross-functional technical committees. Identify potential risks or delays in regulatory timelines and communicate them to relevant stakeholders. Prepare project updates, reports, and documentation to support internal communication and governance processes. Contribute to continuous improvement of regulatory project coordination processes and tools. Qualifications University degree in life science, medical science, pharmaceutical, engineering, chemistry or biotechnology. At least 2 years of experience in regulatory affairs, quality or compliance with Medical Devices. Advanced knowledge of medical device international regulations and environment. Strong organizational and communication skill, self‑motivated, detail‑oriented and capable to work independently. Capability to react quickly to changes in the regulatory environment. Precise planning and execution to achieve accurate and timely results. Ability to manage multiple priorities. Self‑motivated and capable of working with supervision and guidance. Fluent in English (written and spoken). Advanced knowledge of MS Office. Bausch & Lomb is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates. #J-18808-Ljbffr
Bausch + Lomb in County Waterford, Ireland, is seeking a highly technical Lens Manufacturing Engineer (Injection Moulding) to support and improve injection moulding systems in a medical device manufacturing environment. The ideal candidate should have a Bachelor's Degree in Engineering and 3–5 years of experience in a similar role, with strong expertise in injection moulding and a focus on continuous improvement. This position involves hands-on technical support and compliance with health and safety regulations. #J-18808-Ljbffr
Bausch + Lomb is seeking a Regulatory Affairs Specialist based in Dublin, Ireland. This hybrid position involves coordinating regulatory support across global markets and collaborating with local and regional teams to ensure compliance with regulations. Responsibilities include managing project timelines, maintaining documentation, and representing Regulatory Affairs in technical committees. Candidates should hold a degree in life science or a related field and have at least 2 years of experience in regulatory affairs with medical devices, along with strong organizational skills and fluency in English. #J-18808-Ljbffr
Responsibilities to include (but not limited to): As an apprentice you will be required to complete a structured four-year training program in conjunction with SOLAS and WWETB (formally FAS) dependent of results and performance. This will involve block releases to SOLAS and WWETB for specific training in the applicable trade, i.e. Electrical. You will work with the Maintenance Technicians within B+L who will help you develop the skills learned in each block release and also prepare you for the next block release. You will be based in the Maintenance Department, but on occasion may have to support other applicable departments, to develop your knowledge and understanding of your trade. Ensure compliance with all associated EHS regulatory conditions and all corporate B+L guidelines standards policies and operating procedures. Key cGMP Responsibilities Follow Standard Operating Procedures at all times Follow required applicable Regulatory standards as required Participate fully in all GMP and operational training programs and complete all training records in an accurate and timely manner Follow Gowning Procedures and entry rules for all manufacturing and other controlled areas. Understand and follow Personal Hygiene Rules as defined in the GMP Training Programme and notify area supervision of any health conditions which may affect the quality of product. Maintain work areas in a clean and tidy manner at all times. Requirements Leaving Certificate with minimum pass in Ordinary Maths. Leaving certificate in Engineering or Technical Drawing - advantageous. Decisive, self-motivated and capable of working on their own initiative. High level of commitment to training & development. Ability to work as a team member. Bausch & Lomb is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates. #J-18808-Ljbffr
Bausch + Lomb in Dublin is seeking an apprentice for a structured four-year training program in collaboration with SOLAS and WWETB. The role involves working with Maintenance Technicians to develop skills essential to the trade. Candidates must hold a Leaving Certificate with a pass in Ordinary Maths; a background in Engineering or Technical Drawing is a plus. The company values a strong commitment to training, compliance with guidelines, and the ability to work autonomously and as part of a team. #J-18808-Ljbffr
Bausch + Lomb seeks a CMO Relationship Manager in Dublin, responsible for orchestrating the supply chain portfolio, ensuring reliable demand fulfillment, and leading a high-performing team. The ideal candidate has 5+ years of direct management experience and substantial background in supplier relations, operational excellence, and risk management. Strong communication and strategic leadership skills are essential. The role offers opportunities for significant impact across functions and continuous improvement initiatives. #J-18808-Ljbffr
CMO Relationship Manager (Supply Chain) Main Purpose The CMO Relationship Manager holds end-to-end accountability for both the operational execution and strategic direction of the supply chain portfolio to ensure reliable demand fulfilment and supply continuity from external manufacturing. Responsibilities Accountable for the overall performance, governance, and optimisation of the assigned portfolio, including full leadership responsibility for direct reports. The role drives team effectiveness, capability development, and performance management to deliver against business objectives. Acts as a key cross‑functional leader, providing strategic direction and alignment across stakeholders including Regulatory Affairs, Procurement, Finance, and Quality. Ensures robust decision‑making, risk management, and seamless execution across the end‑to‑end supply chain. Partners closely with senior leadership to drive operational excellence, lead critical initiatives, and deliver continuous improvement, while maintaining ownership of day‑to‑day operations and key projects. The CMO Relationship Manager will assist the Senior Manager with day‑to‑day operations and strategic projects. Lead and develop a high‑performing supply chain team, driving accountability, capability building, and delivery of external manufacturing objectives. Own overall supply performance, ensuring consistent achievement of service levels, including supplied in full and on time, through proactive planning and execution. Own and govern key supplier and customer relationships at a strategic level, ensuring supply continuity, effective issue resolution, and alignment with business priorities. Drive performance through structured engagement and escalation where required. Oversee and continuously improve supplier and portfolio performance, leveraging KPI frameworks to identify risks, drive accountability, and implement targeted performance improvement plans. Provide strategic oversight of contractual compliance, ensuring full alignment with customer and supplier agreements, proactively managing risks, and driving timely resolution of any deviations. Lead cross‑functional demand and supply governance forums, ensuring clear alignment on priorities, risks, and mitigation plans. Drive decision‑making, accountability, and timely communication across internal and external stakeholders. Act as a senior interface across the end‑to‑end supply chain, building and maintaining strong, influential relationships with key stakeholders including Manufacturing, Labelling, Regulatory Affairs, Quality, Procurement, and Finance. Drive supply chain excellence through data governance and system integrity, ensuring robust processes, accurate data management, and audit‑ready documentation. Play a key leadership role in Technical Transfers and New Product Introductions, ensuring delivery against timelines, contractual requirements, and business objectives, with proactive risk escalation and mitigation. Own and drive Change Control activities across the portfolio, ensuring alignment with regulatory requirements and successful execution of product changes and launches. Champion continuous improvement and operational excellence, leveraging root cause analysis and structured problem‑solving to enhance supply chain efficiency, resilience, and performance. Ensure full compliance with internal SOPs, regulatory requirements, contractual obligations, and company policies (including SOX), embedding a strong culture of compliance and governance within the team. Maintain oversight of end‑to‑end order management processes, ensuring seamless execution from order intake through to delivery and financial closure, while driving process optimisation and automation where possible. Take on additional leadership responsibilities and strategic initiatives as required, contributing to the broader success of the function and organisation. Person Specification 5+ years Direct Team/People management experience essential with demonstrated experience in leading teams and developing high‑performing talent. 812+ years of progressive experience in managing Suppliers, preferably within pharma, medical devices, or other regulated industries. Proven track record in external manufacturing / CMO management and complex, multi‑site supply chains. Strong background in supplier relationship management (SRM) and performance governance. Experience in New Product Introduction (NPI), technical transfers, and change control. Core Capabilities Strategic leadership: able to set direction, operate in ambiguity, and influence senior stakeholders. Supplier management: drives accountability, performance improvement, and supply continuity. Risk & governance: experienced in managing supply risks within GMP/SOX environments. Operational excellence: KPI‑driven with a focus on continuous improvement and efficiency. Education & Qualifications Degree in Science, Supply Chain, Engineering, Business, or related field. Professional certifications (APICS, Lean Six Sigma, PMP/PRINCE2) are advantageous. What We Are Looking For A highly accountable leader with strong ownership mindset. Excellent communicator with the ability to influence across functions. Resilient and proactive, with a solution‑oriented approach. Equal Employment Opportunity Statement Bausch & Lomb is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates. #J-18808-Ljbffr
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. This position is based in Waterford. Responsibilities Manage and control all aspects of utilities/facilities services, so that all facilities equipment is maintained to a high degree of efficiency. Provide all processes with a standard of service to meet required volume & yields (average monthly/annualized targeted uptime minimum 99.94%). Ensure that all safety and plant equipment are properly maintained and ready for operation. Ensure utilities/ facility systems are robust to ensure acceptable compliance to national, international, and regulatory standards. Participate in problem solving activities RCAs, 5 Whys, etc. in documentation of Facilities related issues and CIPs for the department. Operate utilities/facilities services efficiently and effectively, so that budgeted & non-budgeted cost reductions can be achieved. Provide mechanical support to Facilities Engineering Group and also Technical Services for the execution of Facilities capital projects. Assist Plant Facilities / Project Engineers with system re-design and optimization of plant services & equipment. Requirements Degree in Building Services /Mechanical Engineering or in an equivalent engineering discipline is desirable. 3+ years’ experience in a manufacturing industry desired. Experience of H.V.A.C., Purified Water, Compressed Air, Steam, and general building services essential. Must be familiar with the regulatory and statutory requirements of the FDA, ISO and HSA. Decisive, good communicator, self-motivated. Bausch & Lomb is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates. #J-18808-Ljbffr
A global eye health company based in Waterford is seeking a Utilities and Facilities Manager to oversee all aspects of facilities services. The ideal candidate will have a degree in Building Services or Mechanical Engineering, along with 3+ years of experience in manufacturing. Key responsibilities include managing utilities services, ensuring compliance with regulatory standards, and operating efficiently to achieve cost reductions. The position requires experience with HVAC and good communication skills. #J-18808-Ljbffr
