CQV Engineer
CQV Engineer
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Salary Not Disclosed
1 Vacancy
Job Description
Review and approve documentation related to qualification and testing.
Assist in the assessment of system performance to ensure compliance with regulatory requirements and industry best practices.
Assist in ensuring that processes and systems are validated and maintained in accordance with applicable regulations (e.g. FDA EMA ISO).
Review validation documentation for completeness and compliance.
Documentation and Reporting:
Support the preparation of final reports and deliverables that detail commissioning qualification and validation results.
Ensure that all documentation is compliant with regulatory standards and industry guidelines.
Collaboration and Communication:
Familiarity with industry standards such as GxP FDA and ISO regulations.
Strong attention to detail and documentation skills.
Good problemsolving abilities and a proactive attitude.
Effective communication and teamwork skills.
Ability to work in a fastpaced regulated environment.
Employment Type
Full Time
