Commissioning & Qualification Consultant (Parenteral/Aseptic Process)
About this role
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
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.
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