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Form of work
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 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.
Objectives/Purpose of Job:
Primarily responsible for compiling data, performing data analytics, and publishing annual product reviews for each product manufactured within the review period.
Will also be responsible for various Quality System process improvements and Quality Assurance/System projects and will work with cross-functional teams to develop improve Quality Systems processes.
Key Activities/Responsibilities:
GMP Training:
- Prepares and publishes the Annual Product Review (schedule) at the start of each calendar year.
- Compiles data using various systems such as CATSWeb, D2, ERPLx, GLIMS, ScienTek and other systems that hold product quality information and related records.
- Receive and compile related data provided by other departments relative to the product being reviewed.
- Ensure timely approval and publication of APRs in conjunction with the APR schedule.
- Participate in investigations stemming from APRs and document accordingly.
- Complete assigned training by the assigned due date.
- Performs other duties as assigned.
Qualifications/Training:
- Minimum of BA/BS.
- 3+ years' experience in Quality Systems in a pharmaceutical manufacturing organization.
- Knowledgeable user of statistical software.
- High level of competency of MS office applications such as MS Word, Excel, and Access.
- 3+ years of experience Pharmaceutical Manufacturing GMP Environment or equivalent.
This position may be available in the following location: Tampa, FL.
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: 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.
