Descripción del Empleo:
Develop all plans and execute Installation Qualification for a new production line. Develops expertise knowledge of all factors that make a process to support the response to highly technical questions and situations, to solve quality issues, to improve process, or to confirm reliability of products. Supports equipment development efforts for new devices, and process improvements. These efforts may be the internal development of process equipment or coordination with an external equipment integration company.
Bachelor’s Degree in Engineering. 3+ years of manufacturing experience in pharma or medical device directly executing validation/process qualification activities. Fluency speaking and writing in English and Spanish. Ability to work independently with general supervision on larger, moderately complex projects / assignments. Six Sigma Certification is a plus. ***Experience with Validations/Qualifications is required.***