Projects Documentation

About the role

The Projects Documentation role involves managing technical documentation for a pharmaceutical manufacturing environment. The successful candidate will ensure all project-related protocols and reports meet regulatory and quality standards.

Responsibilities

• Preparation of URS, DQ, IQ, OQ, and PQ protocols and reports for process equipment, utility systems, HVAC systems, and water systems in compliance with GMP requirements.
• Preparation, review, and revision of SOPs for the Projects Department as per QA requirements and regulatory compliance.
• Preparation and review of Project BOQ and technical specifications.
• Checking and verification of instrumentation documentation.

Required skills

• URS
• DQ
• IQ
• OQ
• PQ
• GMP
• SOP
• BOQ
• Technical specifications