Senior Validation Technician – GMP & Sterilization

Bausch & Lomb GmbH; Greenville, Northern (SC, KY); Hybrid; USD 52,000 - 76,000; Full time

Job summary

Bausch + Lomb in Greenville, SC seeks a Validation Technician to support the Site Validation Master Plan, performing re-qualifications and related validation activities.

The role requires collaboration with operations, microbiology, chemistry, metrology and maintenance to ensure GMP compliance and data integrity in all validation work.

Experience in pharma/medical devices and an Associate or BS in science is preferred; familiarity with Ellab data loggers is a plus.

Qualifications

• Associate Degree in Science preferred; BS desirable.
• 0-3 years in validation; 5 years in Pharma/Medical device industries with manufacturing or QC lab experience.
• GMP and Data Integrity knowledge; strong communication and interpersonal skills.

Responsibilities

• Lead validations for routine re-qualifications of steam sterilizers, line sterilization, heat sterilization, aseptic simulations.
• Re-qualifications require entry to aseptic areas and use of Ellab Datalogger or equivalent.
• Author validation strategies, protocols, execute validations, analyze data and write final reports.
• Conduct periodic reviews of validated equipment and systems per SVMP.
• Peer reviews of validation packages and provide feedback.
• Collaborate with operations, microbiology, chemistry, metrology and maintenance.

Skills

Self-Driven

Verbal and Written Communication

GMP and Data Integrity knowledge

Interpersonal skills

Results Oriented

Quality mindset

Education

Associate Degree in Science

Bachelor of Science

Tools

Ellab data logger

Job description

Bausch + Lomb in Greenville, SC seeks a Validation Technician to support the Site Validation Master Plan, performing re-qualifications and related validation activities.

The role requires collaboration with operations, microbiology, chemistry, metrology and maintenance to ensure GMP compliance and data integrity in all validation work.

Experience in pharma/medical devices and an Associate or BS in science is preferred; familiarity with Ellab data loggers is a plus.