Aseptic Process Validation Engineer I

Join a global leader in eye care, committed to helping people see brilliantly. This is a great development opportunity Aseptic Validation Engineer I to grow your career in a cutting-edge lab environment with the world's largest vision care company.

Aseptic Process Validation Engineer I Location :

Houston, TX Duration:

18 months - Extension or conversion potential

Benefits:

Medical, Dental, Holiday, PTO 401K matching We are hiring an Aseptic Process Validation Engineer I Seeking an engineer to support aseptic process and sterilization validation activities in a GMP-regulated medical device environment.

Responsibilities:

Support

IQ/OQ/PQ

validation activities Assist with EO and gamma sterilization validations Investigate validation discrepancies and support CAPA activities Manage change controls and ensure ISO/FDA compliance Partner with cross-functional teams on validation projects

Qualifications:

BS Science/Engineering Experience in pharmaceutical or medical device manufacturing Knowledge of

GMP, ISO

11135/11137, and ethylene oxide and gamma sterilization processes Knowledge of statistical analysis. Strong troubleshooting and documentation skills This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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