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Senior Validation Engineer
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- Primarily responsible for the support and execution of laboratory equipment qualification and associated computer system validation activities in compliance with current cGMP regulations and the clients corporate principles, quality policies, standards, and core values.
- You will work closely with instrument vendors, facilities, IT, and lab personnel to coordinate installation and qualification including computer system validation, of QC Equipment.
- Bachelor's degree (Life Science, Engineering)
- Experience (may vary depending on site size/scope)
- Three to six years of validation experience (or equivalent experience) in a cGMP environment with increasing levels of responsibility for a wide range of validation projects including validation of large-scale biochemical manufacturing, utility, and automation systems.
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