Senior Engineer Process Validation
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POST DATE 8/12/2016
END DATE 12/19/2016
JOB DESCRIPTION6 YEARS OF EXPERIENCE IN VALIDATION OR QUALITY DEPARTMENTS. OR AN EQUIVALENT COMBINATION OF EDUCATION AND EXPERIENCE
*Knowledge of the regulatory and cGMP regulations for pharmaceutical manufacturing operations, and validation procedures and practices
*Excellent verbal and written communication, interpersonal and communication skills required
*Demonstrated ability to develop and present site-wide training sessions
*Ability to communicate knowledge to peers and colleagues from other departments requiring a thorough understanding of equipment, and analytical methods used in GMP environment
*Demonstrate knowledge of basic statistics
*Demonstrates enthusiasm for learning
*Appropriately allocates effort among several goals
*Exhibits sound judgment by: evaluating problems thoroughly, soliciting input and ideas, and using a systematic decision making approach
*Appropriately challenges the status quo and uses knowledge and experience to continuously improve work processes
*Takes ownership of own development.
CANDIDATE MUST HAVE:
BA or BS in Biology, Biochemistry, or related science or engineering disciplines,6 years of experience in Validation or Quality Departments