Document Control Administrator

2 weeks ago


St Louis, United States Bausch + Lomb Full time

Document Control Administrator 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 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: Administer the Document Management Operations at the St. Louis Tree Court and Sovereign Court facilities. Ensure that the Document Control process is conducted in accordance with federal, state, local and applicable regulations, and standards, as well as in accordance with internal Bausch + Lomb policies and procedures. Responsibilities: Review procedures, specifications, and engineering drawings for required changes. Process document changes in a timely manner. Train and assist users as required in use of the Document Management System Filing and organization of Validations, Reports, SOPs, Drawings, RIIs, ensuring that the files are maintained as part of Quality Records Copy, scan and file documents as necessary. Archive records as required into the Document Management System. Maintain Periodic Review Process Assist with processing deviations, issuing/retrieving and tracking. Assist in document retrieval for internal and external audits. Support project teams with documentation needs. Special projects and other related duties as assigned. Qualifications: Required Education: High School Diploma or equivalent. Preferred Education: Associates degree in Technical Field or related Required Skills / Qualifications: Ability to operate office equipment; experience with Microsoft Office Suite; Quality Systems - Document Management Preferred Skills / Qualifications: Statistical training including trends, pareto and other basic charting techniques. Required Qualifications: Minimum three (3) years directly related medical device manufacturing preferably in a Quality Assurance position. 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 This position may be available in the following location(s): US - St. Louis (Tree Court) 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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