Documentation Engineer – Pharma Equipment

Department: Production
Experience: 4+ Years
Qualification: Diploma / Bachelor’s Degree in Mechanical Engineering
Employment Type: Full-Time

Role Summary

Manage technical and validation documentation for pharmaceutical equipment projects by preparing compliant documentation, supporting validation activities, and ensuring document control throughout project execution.

Key Responsibilities

• Prepare DQ, IQ, OQ, PQ, URS, FAT, and SAT documentation.
• Maintain validation records, technical documents, and compliance files.
• Coordinate with Design, Production, QA, and Project teams.
• Ensure document control, version management, and traceability.
• Support customer audits, validation, and regulatory compliance.
• Maintain accurate documentation throughout the project lifecycle.

Required Skills

• Experience in DQ, IQ, OQ, PQ, URS, FAT, and SAT documentation.
• Strong technical writing and documentation skills.
• Knowledge of GMP, validation, and document control practices.
• Proficiency in MS Office and engineering documentation.
• Good coordination, attention to detail, and problem-solving skills.