Planning Engineer

Jain International Trade Organisation - India; Faridabad District; On-site; INR 300,000 - 450,000; Full time

Job summary

Jain International Trade Organisation - India is looking for a full-time Documentation Engineer in Faridabad. This role focuses on preparing and managing technical documentation related to HVAC systems in pharmaceutical facilities, ensuring compliance with GMP and other standards.

The ideal candidate will handle SOPs, IQ/OQ/PQ protocols, and work closely with various teams to guarantee documentation accuracy.

Qualifications

• Detail-oriented Documentation Engineer with knowledge of HVAC systems for pharmaceutical facilities.
• Experience in preparation, review, control, and management of technical documentation.
• Understanding of GMP, cleanroom standards, and pharmaceutical engineering practices.

Responsibilities

• Develop SOPs (Standard Operating Procedures).
• Prepare IQ/OQ/PQ protocols and reports.
• Create DQ (Design Qualification) documents.
• Draft URS (User Requirement Specifications) and validation documents.
• Document preventive maintenance procedures and change controls.
• Coordinate with engineering, QA, validation, production, and maintenance teams.
• Ensure documentation compliance with GMP guidelines, FDA regulations, WHO standards, and ISO.

Skills

Basic Computer Knowledge

MS Excel

Communication Skills

Coordination

Documentation Handling

Time Management

Problem Solving

Adaptability

Technical skills related to HVAC

Job description

Job Type: Full Time Permanent

Location: Faridabad

Work Mode: Onsite

Experience: Entry Level

Skills:

• Basic Computer Knowledge
• MS Excel
• Communication Skills
• Coordination
• Documentation Handling
• Time Management
• Problem Solving
• Adaptability
• Role-specific technical skills (as per department)

We are seeking a detail-oriented Documentation Engineer with experience in HVAC systems for pharmaceutical facilities. The role involves preparation, review, control, and management of technical documentation related to HVAC design, qualification, validation, and compliance in regulated pharma environments. The candidate should have knowledge of GMP, cleanroom standards, and pharmaceutical engineering practices.

Responsibilities

• SOPs (Standard Operating Procedures)
• IQ/OQ/PQ protocols and reports
• DQ (Design Qualification) documents
• URS (User Requirement Specifications)
• HVAC validation documents
• Preventive maintenance procedures
• Change control and deviation documents
• Coordinate with engineering, QA, validation, production, and maintenance teams
• Ensure documentation compliance with GMP guidelines, FDA regulations, WHO standards, ISO and cleanroom standards