Commissioning & Qualification Consultant (Parenteral/Aseptic Process)

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.