Bausch + Lomb Corporation, (NYSE/TSX: BLCO), is solely 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 company is one of the best-known and most respected healthcare brands in the world, offering the widest and finest range of eye health products including contact lenses and lens care products, pharmaceuticals, intraocular lenses, and other eye surgery products.

Our highest priority is the well-being of the people we serve. By listening to our customers and patients, by constantly honing our innovation edge, by executing with integrity and excellence, we strive to earn the trust of our partners and stakeholders.

Over the last 167 years, Bausch + Lomb has become a global hallmark for innovation and quality. Our talented and motivated colleagues work relentlessly to invent new materials, engineer new technologies, and ultimately bring new innovations to help people see better to live better.

This position is based in Dublin.

This is a two-year contract position.

To lead our cross-functional team in the remediation of products to comply with the European Union Medical Device Regulation (EU MDR). The successful candidate will be responsible for overseeing the project lifecycle, managing risks and issues, collaborating with peers across multiple projects, and maintaining clear communication with all stakeholders.

• Lead a cross-functional team in the strategic planning and execution of product remediation projects to ensure compliance with EU MDR.

• Collaborate with department heads and project managers to identify intersections among projects and leverage synergies.

• Develop and maintain comprehensive project documentation, including project plans, risk assessments, and progress reports.

• Proactively identify, analyze, and manage project risks and issues, implementing effective mitigation strategies.

• Facilitate regular project meetings to monitor progress, address challenges, and ensure alignment with project objectives.

• Communicate effectively with stakeholders at all levels, providing regular updates and ensuring transparency throughout the project.

• Ensure project deliverables meet quality standards and comply with regulatory requirements.

• Manage project budgets, timelines, and resources to achieve project goals efficiently.

• Other duties as assigned by Global Quality Director - Programmes

Desirable

• Bachelor’s degree in Project Management, Engineering, Business Administration, or related field.

• Proven experience in project management, specifically in regulatory compliance or medical device industry.

• Project Management education and experience.

• Strong understanding of the EU MDR.

• Excellent leadership, communication, and interpersonal skills.

• Ability to lead and motivate cross-functional teams to achieve project objectives.

• Proficient in project management software and tools

• Decisive, self-motivated/capable of working on own initiative, and able to prioritise and a proactive approach.

The masculine is used in this publication without prejudice for the sake of conciseness.

Bausch & Lomb is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates.

We are an equal opportunity employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply. Accommodations for job applicants with disabilities are available on reques.