Pharma SOP Technical Writer

Pharma SOP Technical Writer – Job Description

Position: Senior Technical Writer – Pharma / Digital Compliance

Experience: 10+ Years

Duration: Immediate need through December 2026

Location: India

Work Mode: Remote

Domain: Pharmaceutical / Life Sciences

Role Type: Contract

Position Summary

We are looking for a Senior Technical Writer with strong experience in SOPs, Work Instructions (WI), Job Aids, compliance documentation, and training content . Pharma/Life Sciences experience is strongly preferred.

The ideal candidate will support Digital Compliance, AI, Data, and Software Development Lifecycle (SDLC) initiatives and work with project teams to ensure documentation and deliverables meet regulatory and organizational compliance expectations.

Key Responsibilities

• Author, develop, revise, and maintain SOPs, Work Instructions (WIs), Job Aids, guidance documents, templates, and training materials .
• Support digital project teams with SDLC requirements, deliverables, documentation, and compliance expectations .
• Develop documentation for Digital, AI, Data, and technology-related compliance processes .
• Review existing procedures and identify opportunities for improvement, standardization, and simplification.
• Coordinate and track SDLC-related deliverables and governance initiatives .
• Work closely with QA, Compliance, IT, Data Governance, and Digital/Technology teams.
• Translate complex technical and compliance requirements into clear, structured, user-friendly documentation .
• Develop training materials and supporting content for new or revised procedures.
• Ensure documentation follows established quality, compliance, and document-control standards .
• Participate in reviews, approvals, and revisions of controlled documents.

Required Skills

• 10+ years of Technical Writing / Documentation experience .
• Strong hands-on experience creating:
• SOPs
• Work Instructions (WI)
• Job Aids
• Policies / Procedures
• Guidance Documents
• Training Materials
• Templates
• Strong Pharma / Life Sciences / Healthcare experience preferred.
• Experience working in QA, Quality, Compliance, CSV, GxP, or regulated environments .
• Understanding of SDLC processes and documentation requirements .
• Strong ability to work with technical and business stakeholders.
• Excellent written and verbal communication skills.

Regards

View phone number on foundit.in

Sourabh