Description
CSV/Data Integrity Specialist - 389839 (m/f)
Reference: -en
Start: asap
Duration: 24 MM+
Main tasks:
- Management of Computer System Validation Projects for laboratory equipment as well as manufacturing equipment
- Develop, review and approve Validation Plans, Specifications, Test Scripts, Installations Qualification Protocols, Operational Qualification Protocols, Performance Qualifications Protocols, Traceability Matrices and Summary Reports
- Perform Computer System Validation tests
- Generate/review Standard Operating Procedures related to Computer System Validation Process and Data Integrity
Main qualifications
- Bachelors or Master degree in Engineering, Life Sciences or another closely related discipline
- Profound work experience in pharmaceutical environment
- Significant practical experience in Computer System Validation
- Strong project management skills with the ability to prioritize assignments
- Fluent in English
Main advantages:
- A very renowned company
- You will work in an international environment
- High degree of personal responsibility
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
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