Computer System Validation
Job
Programming.com
Mexico, MO (In Person)
Full-Time
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Job Description
4+ years of hands-on CSV experience in pharma, biotech, or CRO Deep understanding of GCP/GLP processes and regulatory expectations Proven track record preparing systems and documentation for regulatory audits Strong documentation, communication, and problem-solving skills Overview Industry
- IT•Consulting Services / Advisory Services Functional Area•Other Job Role•Other Employment type•Full Time Work Mode•Hybrid Qualifications Any Graduate•Any Specialization Any Post Graduate•Any Specialization Any Doctorate•Any Specialization Job Related Keywords Computer System Validation Computer System Computer system validation
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