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The Mission
System Validation
Perform meticulous qualification of pharmaceutical production equipment and software systems to meet stringent GMP standards.
Protocol Development
Author and execute IQ/OQ/PQ protocols with a sharp focus on comprehensive documentation, technical accuracy, and risk mitigation.
Compliance
Ensure all validation and engineering activities adhere to ALCOA+ data integrity principles and global regulatory frameworks.
Collaborative Quality
Work closely with cross-functional teams to resolve complex quality deviations and continuously optimize internal validation workflows.
Meaningful pharma projectsÂ
Work on projects that have real impact on pharmaceutical quality, compliance and ultimately patient safety.Â
Technical & Professional growthÂ
Build your expertise through a personal training program, hands-on experienceÂ
and exposure to different validation methodologies, technologies and GxP environments.Â
Autonomy & TrustÂ
Work across different sites, systems, equipment and clients. We give you freedom to useÂ
your expertise, make decision and find solution, so you can take ownership of your work. Â
Competitive PackageÂ
A competitive salary combined with a comprehensive benefits package, mobility options, insurance, flexibility and all the tools you need to do your job well.Â
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