Pharma CQ/CSV Lead - Commissioning & Validation

Full-time Company Description Validation & Engineering Group,Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical,and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services. Job Description Serve as focal point for Commissioning & Qualification and/or Computer System Validation (CSV) in assigned project. Work on multi-discipline engineering capital project teams, as well as other project-related, cross-functional teams with representatives from departments throughout the organization. Manage assigned project goals within scope, on budget, and on schedule. Communicate proactively with stakeholders and senior management regarding progress, issues, and plans for resolution. Development and execution of C&Q/CSV Strategies and Validation Documents. Qualifications Bachelor Degree in Engineering or Science. 3 to 5 years of experience in C&Q for Manufacturing Equipment or Facilities CSV Experience is a plus Experiences in Quality Systems Must have at least 3 to 5 years of experience in the the pharmaceutical, biotechnology or medical device industries. Additional Information Positions availablefor Puerto Rico. Validation and Engineering Group, Inc is an Equal Employment Opportunity employer. By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply #J-18808-Ljbffr Validation & Engineering Group