Quality Application/ Validation Specialist

Quality Applications/Validation SpecialistLOCATION: JUNCOS, Puerto ricoType: Full Time Positions Available: One (1)QUALITY CONSULTING GROUP, a leader inthe pharmaceutical, biotech, medical devices and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico.You'll be a fit for this job if you have:Bachelor’s degree in Sciences or Engineering3 years of related experience Exposure to Validation ActivitiesFully Bilingual English/Spanish – Written is required.In this position you'll: Develop and/or review Validations Documents (Master Validation Plans/Reports, Test Method Validations, IQ, OQ and/or PQ), Execute Validations in assigned Manufacturing Areas, and generate Reports. Document and execute IQ for label printing, Review Manufacturing processes changes through CCB. Able to implement and/or review EU MDR requirements (such as PIC card implementation, Manufacturing/PFMEA changes and other required activity per EU MDR requirements). Develop and/or revise PPM as required Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate federal regulations.To get hired at QUALITY CONSUTING GROUP, you MUST be:Validation process (PQ, OQ, Test Method validation)The details:We're a growing 60+ person company.We are actively looking for the best candidate.We accept applications and RESUME’s to: **********wered by JazzHR