Description
Overseas Opportunity- 6 months in the Sun
Our client, a global biopharmaceutical organisation require a QAV Engineer/ Validation or Document Reviewer to work on their major sterile filling line site internationally.
Working on a site in India, you will be responsible for the review of Validation Documentation and execution of IQ OQ PQ for sterile filling line equipment.
- You will be one of a number of experts on site guiding and helping local staff overseeing them in their work and directing them.
- Providing Validation expertise for the validation lifecycle of new filling lines and retrospective work on existing lines.
Experience
Require Consultants with lots of experience in Process and Cleaning, equipment validation both in document review and execution.
Strong background in equipment validation including: autoclaves, depyrogenation tunnel/ oven, filling machine
Extensive documentation review experience, protocol writing, review and sign off.
This s an excellent role offering local accommodation, regular rotations home, competitive rates.