Este perfil está escrito en inglés
Demonstrated experience with SOP Authoring.
Demonstrated experience with Technical/Regulatory Documentation.
Demonstrated experience with Document Review & Finalization.
Demonstrated experience with Data Consistency & Integrity Checks.
Demonstrated experience with ISO/IEC 17025:2017.
Professional profile
Authored and quality-controlled technical documentation and SOPs governing ~6,000 annual test records, ensuring document accuracy, consistency, and adherence to defined regulatory standards prior to distribution.. Acted as project lead and primary point of contact for 7 accredited facilities during document review cycles, coordinating cross-functional input from technical teams and external auditors, negotiating resolution timelines, and driving 100% closure of findings within fixed 30-day cycles.. Served as Authorised Signatory, personally reviewing and finalizing documents for regulatory submission accuracy and completeness before external release.. Led a 50-person team and mentored junior staff in SOP authorship and documentation standards, building department-wide templates and guidelines still in use.
Authored and finalized 150–200 validated diagnostic reports daily, applying structured review and quality-control checks against strict biosafety and public-health regulatory protocols within a ~2-day turnaround.. Reviewed data outputs (amplification curves, Ct values) for consistency and integrity before finalizing reports for regulatory and public health authorities, escalating discrepancies for resolution.
Authored SOPs, quality manuals, and validation reports supporting NABL accreditation; led method validation studies producing documentation later used as the evidentiary basis for external accreditation review.. Directed internal audits and supervised a 5-person team, applying structured document review to close all findings within 30 days.
Took leave from full-time employment for family care responsibilities following the birth of a second child, without access to maternity leave. Returned directly into high-intensity pandemic diagnostics documentation work in mid-2020.