Validation & Engineering Group, Inc. logoValidation & Engineering Group, Inc. logo

Commissioning & Qualification Consultant for Parenteral/Aseptic Processes

On-site Full-time

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Experience Level

Mid to Senior

Qualifications

To be successful in this position, you must possess the following qualifications:Bachelor's degree in Engineering or Science is required. Minimum of 8 years of experience in Commissioning and Qualification (C&Q) for manufacturing equipment and processes. Experience in Computer System Validation (CSV) is a plus. Must be fully bilingual (English/Spanish). Exceptional technical writing skills are essential, along with the willingness to execute validations during different shifts and weekends. Proven experience with aseptic filling processes, specifically in parenteral manufacturing and sterile product filling. At least one of the following experiences is required: Process Validation, Media Fills, Smoke Profiles, Classified Room Performance Qualification, Environmental Monitoring, or Aseptic Filling.

About the job

Join our dynamic team as a Commissioning & Qualification Consultant specializing in parenteral manufacturing and aseptic processes. In this role, you will provide critical support for the Validation, Commissioning, and Qualification of manufacturing processes and equipment in your assigned projects. Your expertise will extend to Aseptic Filling Processes, Media Fills, Environmental Monitoring, and various other projects as needed.

About Validation & Engineering Group, Inc.

At Validation & Engineering Group, Inc., we are a leading provider of innovative solutions tailored for the Pharmaceutical, Biotechnology, Chemical, and Medical Device industries. Our expert services encompass Laboratory Compliance, Computer Engineering, Project Management, and Validation, ensuring that our clients achieve the highest standards of quality and compliance in their operations.

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