Job Description
This vacancy is a great career opportunity concerning a new pharmaceutical manufacturing facility associated with a European group.
Job Description:
● Ability to study and use existing standards guidelines to prepare validation , qualification and requalification protocols for production and laboratory eqipment
● Ability to preform validation procedures and support FATs, SATs,DQ/IQ/OQ/PQ as appropriate to the plant , equipment , systems, analytical methods, cleaning and process .
● Coopration in HVAC , water and compressed air systems qualification .
● Prepareing and maintaine a site validation master plan (VMP)
● Evaluateing data from executed validation protocols and ensureing summary reports are generated and approved .
● Paritcipating in and responding to inspections by regulatory authorities and representing the validation procedures .
● Generating or approving Quality Risk Assessment documents and deviations related to validation activities .
● Directly reporting to the QA manager
Factory Location: Kordan, 10 Km of Karaj-Qazvin freeway, Alborz. If you are interested in this offer, please send us your English CV.