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Systems Validation Professional
2 weeks ago
Job Overview
We are looking for a QA Systems and Validation Specialist to join our team. The successful candidate will be responsible for assessing changes for GMP compliance, reviewing and approving design aspects of major capital projects, and implementing quality systems in accordance with ICH Q7, EudraLex, and 21 CFR standards.
Key Responsibilities:
- Qualification of premises, equipment, and utilities
- Computer system qualification, CSV
- Laboratory equipment validation
Requirements:
- Min of BSc/BEng in Chemistry, Engineering or a science-related discipline
- At least 3 years pharmaceutical experience ideally in a QA role
- Knowledge / appreciation of other site operations such as QC, Operations, Engineering, IT