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.
Purpose of the Job
Review and approve data generated by the Greenville QA Chemistry Laboratory to ensure accuracy and reliability of results and raw data used to support product and raw material release, validation/engineering studies, and equipment maintenance. Assist with or lead laboratory investigations, non-conformance investigations and implement corrective and preventative actions.
Key Activities
• Review and approve data generated by the Greenville QA Chemistry Laboratory to ensure accuracy and reliability of results and raw data used to support product and raw material release, validation/engineering studies, and equipment maintenance.
• Ensure data and documentation meets current FDA Regulatory and GMP/GLP standards.
• Perform OOT/OOS and non-conformance investigations and document related NC/LIR/CAPA records in a compliant manner.
• Review and author documents in the D2 Document Management System.
Scope of Position
• The data review technician is responsible for ensuring data and documentation produced by the Greenville QA Chemistry laboratory is accurate, reliable and meets current FDA and cGMP requirements.
• Must be self-directed, have a high level of attention to detail and significant knowledge/understanding of FDA and cGMP laboratory requirements.
Qualifications
• BS in Chemistry or related discipline
• At least five years previous experience in an analytical laboratory within a regulated manufacturing industry.
• Chromatographic techniques (i.e. GC, HPLC/UPLC)
• Compendial (USP, EQ, JP) analysis, techniques and requirements
• Other chemical analysis techniques (titrations, wet chemistry, UV/Vis, FTIR, ICP-MS)
• Method validation and verification requirements
• Equipment validation/calibration requirements
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Previous work in a GMP/ISO laboratory setting is required.
Preferred skills:
• Must have high level of attention to detail and thorough understanding of FDA/cGMP documentation and data integrity requirements.
This position may be available in the following location(s): US - Greenville, SC (Plant)
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.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement .
Our Benefit Programs: Employee Benefits: Bausch + Lomb
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.