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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Skills

Mi
Microsoft Excel
Mi
Microsoft Office
Mi
Microsoft Powerpoint
Mi
Microsoft Word
Sc
Scriptworks
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Experience Level

Microsoft Excel
Expert
Microsoft Office
Expert
Microsoft Powerpoint
Expert
Microsoft Word
Expert
Scriptworks
Expert
Logo
Beginner

Language

English
Fluent
Kannada
Fluent
Telugu
Fluent
Hindi
Beginner

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
    uniE613 "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.