Bachelor's or Master's degree in Engineering, Chemistry, Life Science or related subject with 3+ years of experience in either of the following industries biopharm, medical device and pharmaceutical
A thorough understanding of the GMP regulatory environment, validation, and associated subjects
An ability to work independently and follow instructions
Excellent verbal and written communication skills
Understanding of critical Utility Qualification
Proficiency in Windows and Microsoft Office applications
Knowledge of Kaye(c) Validator / thermal validations a plus
Knowledge of cleaning and process validation a plus
