Validation Technician IV

1 week ago Be among the first 25 applicants

Get AI-powered advice on this job and more exclusive features.

Apply now »

Date: Nov 11, 2025

Location: US-SC-Greenville, US

Company: Bausch + Lomb

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.

Validation Technician will be responsible for supporting tasks outlined in the Site Validation Master Plan (SVMP).

• Lead and coordinate validations for routine re-qualifications of steam sterilizers, line sterilization, heat sterilization, aseptic simulations, sterility isolators that support the SVMP, among others. Re-qualifications require entry to aseptic areas, tank entry and use of Kaye Validator or equivalent.
• Author validation strategies, protocols, execute validations, analyze data and write final reports for projects that support equipment, steam sterilization, process or cleaning validations, among others.
• Conduct periodic reviews of validated equipment and systems as outlined in SVMP.
• Conduct peer reviews of validation packages for fellow team members and provide feedback.
• Perform applicable department responsibilities as defined by Validation Manager and needs of the department.

• Education: Associate Degree preferred, BS desirable.
• Desired use of a Kaye Validator (or equivalent data logger).
• Experience: 0-2 years of validation experience, 5 years in Pharma/Medical device industries with manufacturing or QC lab experience.
• Preferred
  
  Skills:
  
  Self-Driven, Strong Verbal and Written Communication, Strong Interpersonal skills, Results Oriented, quality mindset.
• This position may be available in the following location:
  Greenville, SC.

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.

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.

Apply now »

• Entry level

• Full-time

• Management and Manufacturing

• Medical Equipment Manufacturing