I’m a Technical Writer specializing in creating accurate and regulatory-compliant documentation for pharmaceutical and biopharmaceutical industries. With a background in consulting and experience working with leading clients, I focus on developing:
Standard Operating Procedures (SOPs)
Validation Protocols
Computer System Validation (CSV) Deliverables
My mission is to simplify complex processes and deliver clear, user-friendly documentation that ensures compliance with industry standards (FDA, GMP, etc.) and supports operational efficiency.
I bring a detail-oriented approach and collaborative mindset to every project, working closely with teams to meet your specific requirements. If you’re looking for a dependable writer who understands the unique challenges of the pharma and biotech sectors, I’m here to help.
Let’s work together to achieve your documentation goals!
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