Manager, Quality Systems & Compliance

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 worldfrom 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 nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 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.

Purpose of Job:
Reporting directly to the Site Quality Leader, the Manager of Quality Systems & Compliance is responsible for the maintenance and execution of the Greenville Quality System for the Solutions Facility. In addition, the role is responsible for site compliance to applicable regulations and standards.

Key Activities / Responsibilities:
Oversee and ensure the proper execution of key quality system elements such as records management, document control, change management, CAPA, regulatory and notified body audits, internal audits, supplier audits, training, regulatory management, management review etc.

Will provide direction/leadership to Greenville Operations on cGMP and other compliance requirements.

Ensure that the entire Greenville operation maintains compliance with associated regulations from the site standards list and industry best practices.

Conduct and facilitate internal, regulatory and third-party inspections for the site, including the drafting of response communication from post-inspection follow up, as required.

Interface with outside regulatory and legal authorities as appropriate. Review, revise and approve procedures and specifications, and then communicates and implements them with the applicable department. Manage the training program for the site Act as the site quality lead for data integrity initiatives.

Work directly with the Site Quality Leader to deploy Regional Quality initiatives to the site, conduct gap assessments as needed and provide key input into the development of such initiatives.

Oversee the performance of department staff. Establish, manage and monitor departmental budget and spending against stated variances.

Establish, communicate and execute against strategic quality and site objectives.

Identify, evaluate, select and implement against continuous improvement and compliance initiatives

Scope of Position:
Role has budget responsibility for department spending. Size of Team: 9 personnel. Responsibility is limited to Greenville Location.

Qualifications:
Minimum of a B.S. degree, scientific or engineering degree.

Certifications preferred: CQA, CQE, CQM.

10 years of experience managing quality systems or directly associated with manufacturing or manufacturing quality in a sterile dosage pharmaceutical or medical device facility. (i.e., 21CFR211, 21CFR820, ISO 9001, ISO 13485).

Experience in leading, conducting and writing investigations.

Experience in preparation and execution of GMP regulatory inspections.

This position may be available in the following location(s): [[location_obj]]

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.

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

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