Candidate will be responsible of develops and implements qualification protocols (IQ,OQ,PQ), SOP’s, validation support to ongoing activities, assists in troubleshooting of equipment and deviations. Willing to travel to customers sites in the North are of Puerto Rico or South area Puerto Rico.
|Requisitos - Requirements
-BS in Engineering
-Minimum 3 years in the pharmaceuticals industry
-Developing validation SOP’s
-Validation of PLC/HMI Control Systems
-Effective use of Excel, Word, etc.
-Experience with cGMP’s, FDA regulations
-Excellent verbal and written communication skills in English and Spanish