Commissioning & Qualification Consultant (Parenteral/Aseptic Process)

AI overview

Support the validation and commissioning for parenteral manufacturing processes while executing validations across various shifts and managing aseptic filling processes.

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.