Senior Manager Quality Engineer (Medical Devices and Pharma Experience required)

Senior Manager Quality Engineer (Medical Devices and Pharma Experience required) Full-time Validation & Engineering Group (V&EG) is a leading services supplier that provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. Accountable for providing Quality oversight of FP Technologies method stewardship, modeling, and material characterization. Accountable for developing and leading a team that provides Quality technical expertise and assessments of compliance to FP Core Technologies and/or to sites. Ensures successful physical method development critical to achieving reliable data, considering impact of risk to patient, global compliance and time to market. Ensures alignment strategies for methods transfer across multiple sites. Works with External Supply Quality and/or other quality counterparts to ensure there is a robust plan in place when receiving methods from a CMO or supplier. Provides Quality oversight to final product core technologies activities and deliverables. Quality approval of protocols and technical reports for method development. Masters/Bachelors Degree in Science or Engineering. Qualifications and Skills 5+ years of experience in Validation Qualifications. Combination process / Medical Devices experience. GMP experience (quality management systems, manufacturing). Audits / Inspections experience. Positions available for Puerto Rico. Validation and Engineering Group, Inc. is an Equal Employment Opportunity employer. #J-18808-Ljbffr Validation-