Validation Engineer III - Andover

Only for registered members Andover, United States

1 week ago

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Job summary

The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols, test plans, various computer validation testing documents, deviations,
and change controls in relation to DI remediation activities.

The documentation will span the breadth of validation and change control requirements
for biopharmaceutical processing therefore validation and quality assurance experience in an manufacturing GMP environment is required.


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