
About Me
I am a life sciences professional with hands on experience in biotechnology industry and quality systems within an ISO compliant environment. I specialize in supporting companies with QMS documentation, SOP development, and audit readiness, ensuring alignment with ISO standards and regulatory requirements.
I have practical experience in internal and external audits, documentation control, and compliance processes, and I understand the challenges startups and growing labs face while preparing for certifications and inspections.
I can help with:
SOP writing and QMS documentation
ISO audit preparation and gap analysis
Regulatory and clinical documentation support
Data organization and scientific documentation
I focus on delivering clear, compliant, and practical solutions tailored to your organization’s needs.
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