Your New Job:
As the QA Cleaning Validation Engineer you will be responsible for implementing and executing the cleaning validation program. You will also be responsible for participating as a team member of new product and process introductions from a validation perspective. There will also be a need for you to implement and maintain the re-validation program.
As the QA Cleaning Validation Engineer you will be responsible for generating and executing FAT, SAT, IQ, OQ and PQ protocols and reports in compliance with cGMP requirements, FDA and European regulations. Conducting activities in the following areas as directed by the Validation Co-ordinator: Cleaning Validation, Process Validation, Equipment Validation, Facility & Utility Qualification & Software Validation. You will also be responsible for raising, tracking, and closing out protocol deviations during protocol execution.
What you will Have:
As the QA Cleaning Validation Engineer you will have a BSc or BEng in a relevant discipline with 3 years’ experience working within a cGMP pharmaceutical manufacturing environment.
You will have experience with; NPI from a validation perspective, implementing/ executing a "re-validation" programme, writing/ executing validation protocols (FAT, SAT, IQ, OQ and PQ) and reports.
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