For Validation services in the Engineering area. This role requires a Bachelor's Degree with four (4) years of experience as an Engineer within the pharmaceutical or regulated industry. The ideal candidate will be bilingual (English & Spanish) and possess strong Project Management skills. The shift is administrative, and according to business needs. Experience in Commissioning and Qualification of parenteral products, vision system, device assembly and packaging (Automatic and HMLV lines) is essential. The role also involves completing complex or novel assignments, developing engineering policies and procedures, supervising and coordinating the work of engineers, associates, and technicians, employing advanced engineering techniques, applying knowledge of engineering principles outside of one's discipline, and serving as a peer-recognized engineering technology specialist. Mature engineering knowledge is applied in planning and conducting projects.
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Job Type
Full-time
Career Level
Senior