Role & responsibilities
Prepare, format, revise, and maintain SOPs, work instructions, forms, and controlled documents.
Collaborate with Manufacturing, QA, QC, and Engineering teams to collect technical information and incorporate feedback.
Review documents for accuracy, completeness, consistency, and compliance with approved templates and procedures.
Monitor document revisions, review comments, approvals, and pending actions.
Support document routing, issuance, version control, retrieval, and archival.
Ensure compliance with Positive Documentation Practices (GDP) and applicable GMP requirements.
Maintain well-organized documentation to support daily operations, inspections, and audit readiness.

Preferred Candidate
Experience in pharmaceutical or biopharmaceutical documentation and document management.
Working knowledge of Manufacturing, QA, QC, and Engineering functions.
Familiarity with controlled document processes and Valuable Documentation Practices (GDP).
Robust technical writing, proofreading, organizational, and communication skills.
Proficiency in Microsoft Word and Excel.
Experience with Electronic Document Management Systems (EDMS) is preferred

📌 Pharma Documentation Specialist Hyderabad
🏢 United Consulting Hub
📍 Hyderabad