Thermo Fisher Scientific·3 months ago
3 months ago
QA Validation & Qualification Documentation Reviewer
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About this role
We are expanding our team: As a QA Validation & Qualification Documentation Reviewer, you will ensure the accuracy and traceability of validation and qualification documentation within GMP frameworks. You will review and approve documents for compliance and support cross-functional teams. Ideal for candidates with experience in pharmaceutical validation and strong technical writing skills.
Skills
- process validation
- capa
- stakeholder management
- gmp compliance
- equipment qualification
- technical writing
- facilities qualification
- computerized system validation
- quality assurance
- cleaning validation
- validation documentation review
- change control
- minitab
- deviation management
- statistical software analysis
- utilities qualification
- aseptic process simulation
Company
Thermo Fisher Scientific
Covingham, United Kingdom
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