CAI is seeking a CSV Engineer to develop and execute validation protocols for computer systems in life sciences environments. You will write assessments, URS, FRS, RTM, and summary reports, ensuring compliance with GxP and 21 CFR Part 11.
Travel domestically and internationally as required; strong English communication is essential. Experience with MES, DeltaV, PI, and major systems (Rockwell, Siemens, Honeywell, etc.) is a plus.
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CSV Engineer: GMP Validation for Biotech & Pharma employer: Cagents
At CAI, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of Sydney's leading health and research precinct. Our commitment to employee growth is evident through continuous learning opportunities and a supportive environment where integrity and excellence are at the forefront of everything we do. Join us to make a meaningful impact in the life sciences sector while enjoying the benefits of working with a dedicated team that values your contributions and encourages you to push boundaries.
