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 Good 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 Good 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