• At least with 3-5 years of relevant experience
• Candidates must have working experience with manual testing and preferably also automated testing (selenium based tools).
• Candidates must have working experience with system development life cycle and creating key validation documentation mentioned above.
• Candidates must have ability to multi-task and be flexible in a fast paced environment. Writing test scripts, executing test scripts, attending stand up calls, and following up with project team on outstanding issues or clarifications.
• Candidates must have ability to assist Validation team members. For example: Providing knowledge or sharing experience. Working with other Validation team members writing and executing test scripts.
• Candidates must be able to find better ways of working. Sharing ideas on how our team can be more efficient.
• Candidates must be able to meet project deadlines.
• Clinical/Pharma Industry experience with knowledge of regulatory expectations for computerized systems, 21 CFR Part 11, Annex 11, and related regulations is preferred.
• Candidate must be able to work in the UK work shift.
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