Validation Engineer with a minimum of 3 years experience in pharmaceutical manufacturing equipment and process validations. Candidate will perform equipment and process validation activities for project in printing, leak testing, and PM inspection sub-systems.

ESSENTIAL FUNCTIONS:
Interface with Management personnel in Engineering, Manufacturing, Regulatory Affairs, and other technical disciplines to represent
QA/Validation in project teams, with the objective to assure that project quality objectives are met. Design and execute Validation Plans
and Programs for new and improved pharmaceutical manufacturing processes and products. Design and implement Quality Control
and Quality Assurance systems for new and existing pharmaceutical manufacturing processes and products.
BS degree in an engineering or scientific discipline preferred with minimum of three years of experience in a pharmaceutical QA/QC or Engineering

Knowledge:
Demonstrated knowledge within the areas of Industrial Quality Control, Quality Assurance, and Validation. Demonstrated knowledge in
Industrial Statistics and its application to Pharmaceutical Manufacturing and Quality Control. Expertise in US FDA cGMPs and QSR