you provide support general process validation together with CSV activities
you serve as technical expert for the validation process and responsibilities to ensure compliance
Facilitate successful team behaviour within quality systems and across functional areas for each validation exercise
Ensure all validation activities and documents are authorized and appropriate compliance approval is gained
High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations
Working experience of process validation and software validation for use in a regulated environment
Qualification in an appropriate discipline (e.g. Engineering, Information Systems, or Life Science with additional IT qualification) with a broad technical/educational skills base profound experience in a regulated environment with first experience carrying out validation and/or testing activities
Previous MD experience
Urgent need for a minimum of 6 months with high chances of extension
A highly motivated team and an open way of communication
Über Hays: 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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