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.

Support the Validation, Commissioning & Qualification for parenteral manufacturing process and equipment in the assigned project(s).  May also, support Aseptic Filling Process, Media Fills, Environmental Monitoring and other assign projects.

• Bachelor Degree in Engineering or Science.
• REQUIRED: At least 8 years of experience in C&Q for Manufacturing Equipment and Process
• CSV Experience a plus
• Fully bilingual (MUST)
• Must have: Excellent technical writing; Willing to execute validations on different shifts and weekends. 
• Must have: Experience with aseptic filling process (parenterals manufacturing, sterile products filling process) 
• Must have at least one of the following: Experience with Process Validation, Media Fills, Smoke Profiles and/or Classified Room Performance Qualification, Aseptic filling, Environmental Monitoring.

More Positions available for Puerto Rico and USA.

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.