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.

Objectives:

This position is responsible for support and maintenance of the global quality management system and its compliance for the company through ensuring the process for managing changes/new standards is robust, successfully executed and governed.

Responsibilities:

• Facilitates / coordinates and tracks quality systems compliance with regulatory standards and ensures appropriate actions are escalated if these standards are not met.

• Support the completion of standard assessments to support MDR submissions to achieve on time project timelines.

• Ensuring standard compliance activities are assessed and facilitate remediation activities.

• Effective communication of process metrics and status updates for all BU’s (CL, LC, Sur & Non-NQM-100) to applicable leadership.

• Create/update QMS documentation to support compliance.

• Support Legal Manufacture inspections and readiness including audit records and where appropriate quality system documentation (i.e., NC, CAPA, etc.).

Requirements:

• Bachelor's Degree (science discipline preferred).

• Minimum of 5 years of relevant experience required in global medical device (and/or pharmaceutical) manufacturing organization.

• Experience in Quality Operations/Compliance/Regulatory.

• Project Management skills and experience preferred.

• Highly proficient with Microsoft programs.

• Strong interpersonal and technical writing skills.

We offer competitive salary & excellent benefits including:

• Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date

• 401K Plan with company match and ongoing company contribution

• Paid time off – vacation (3 weeks - prorated upon hire), floating holidays and sick time

• Employee Stock Purchase Plan with company match

• Employee Incentive Bonus

• Tuition Reimbursement (select degrees)

• Ongoing performance feedback and annual compensation review

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

As required by New York State's pay transparency bill, Bausch + Lomb provides a good faith minimum and maximum salary range of compensation for roles that can or will be performed, in New York State. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and specific office location. For New York State, the range of starting annual base pay for this role is $79,000 - $120,000.

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

To learn more please read Bausch+Lomb's Job Offer Fraud Statement (https://hcm2preview.sapsf.eu/bauschhealT4/Bausch_job_posting_statement.docx) .

Our Benefit Programs: https://www.bausch.com/careers/benefits/

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.