Computerised System Validation Specialist
3 settimane fa
We are currently recruiting for our internationally renowned client in the Life Sciences sector, seeking three Computerised System Validation specialists.
The ideal candidate will have at least two to three years of operational experience in the pharmaceutical and/or biotech industry, specifically in CSV (Computerised System Validation), validation protocols, and Validation Plan, IQ/OQ/PQ processes.
Key responsibilities include:
- Independently manage the design and execution of tests.
- Provide client support in software system validation.
- Develop validation plans, conduct tests, collect and evaluate results, and prepare validation reports.
- Management of change control and periodic review processes.
- Conducting data integrity assessments.
Candidates must have demonstrated experience in the pharmaceutical and/or biotech sectors and proficiency in pharma standards and regulations (ISPE GAMP and GxP, EUDRALEX, FDA CFR 21, etc.).
Key Requirements:
- Very good knowledge of pharma standards and regulations.
- Italian and English language skills at CEFR C1 level or higher.
- Utmost professionalism and seriousness towards customers and colleagues.
We offer a rewarding salary pack, growth plan, and attractive bonuses on results-based performance. Join Maasi Enterprises Ltd and be part of our team of professionals committed to excellence in the Life Sciences sector.
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