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!…

Prashanth M

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!…

Available to hire

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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Language

English
Fluent
Kannada
Fluent
Telugu
Fluent
Hindi
Beginner

Work Experience

Add your work experience history here.

Education

Master's in General chemistry at JSS college
June 1, 2014 - August 1, 2016

Qualifications

Life science Certified
October 1, 2024 - January 5, 2025

Industry Experience

Life Sciences, Healthcare, Other
    paper "Experienced Technical Writer | SOPs, Protocols, and Compliance Documentation Specialist"

    I am a skilled technical writer with expertise in crafting clear, concise, and compliant documentation for pharmaceutical and biopharmaceutical industries. My focus areas include:

    Standard Operating Procedures (SOPs)
    Validation Protocols
    Computer System Validation (CSV) Deliverables
    With experience in consulting, I collaborate with cross-functional teams to develop documentation that meets regulatory standards (e.g., FDA, GMP) and ensures operational excellence. I excel at simplifying complex processes into user-friendly content tailored to your business needs.