Descripcion
Responsible for technical support and the overall management of Vision System Integration and/or Manufacturing Equipment Modifications Validation Program at a facility. Provides technical and project leadership for the validation company projects, support of manufacturing operations and for eventual release testing of intermediate and finished products. Develop test method qualification and validation protocols. Develop technical documentation such as: Change Controls, Validation Plans, Validation Protocols, Technical / investigation reports, SOPs, and others.
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Requisitos - Requirements
Minimum of BA or BS in engineering or sciences having a minimum of 3+ years of related experience in Validation Activities. Demonstrated performance within a GMP regulated environment within the pharmaceutical industry. Ability to work effectively with multi-department and multi-site teams. Ability to manage and organize complex technical problems. Good written and oral communication skills, excellent attention to details. Strong team leader with project management skills and focus on results. Excellent skills for redacting Validation protocols and revision of procedures in English. Must be able to work more than 8 hours a day or 40 hours a workweek as required. (26223-3) Various positions available. CANDIDATES MUST HAVE EXPERIENCE IN COMPLETE VALIDATION CYCLE.
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