
Detail-driven Metrology Lead / Technical Specialist with 15+ years in regulated Biopharma, CDMO environments, known for producing, audit-ready documentation and confidently supporting inspections. Versed in technical writing including SOPs, calibration and maintenance procedures, investigation narratives, and scientifically sound rationales that support internal quality expectations.
I bring audit confidence, with the ability to clearly explain, defend data integrity and traceability, and help affected departments, by providing data for inspectors Highly effective in cross-functional communication, I work seamlessly with Facilities Engineering, Validation, QA, Manufacturing, translating technical and regulatory requirements into practical, compliant operations that support quality objectives.