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Over mij
Validation and process engineer with 8 years of experience in GMP-regulated pharmaceutical and biotech environments. I specialize in drafting and reviewing SOPs, validation protocols (IQ/OQ/PQ), batch records, and change control documentation. My work ensures regulatory compliance, operational efficiency, and audit readiness for startups and growing biotech teams. I deliver clear, practical, and compliant documentation, helping organizations meet quality standards while streamlining processes.... Lees meer