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.
Qualifications
- 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.
Additional Information
More Positions available for Puerto Rico and USA.
Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.