About Us:
We are a leading manufacturer of Primary Liquid Filling & Packaging Machinery, serving the Pharmaceutical, FMCG, Food & Beverage industries.

Role & responsibilities

Prepare and maintain validation documentation packages including DQ (Design Qualification), IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification).
Develop and maintain URS, DQ protocols, IQ/OQ/PQ protocols, and final validation reports.
Coordinate with Design, Production, QA, and Project teams to collect and verify technical inputs for validation activities.
Prepare FAT/SAT documentation, commissioning records, and compliance-related technical files.
Ensure data integrity, document control, version management, and traceability as per project and regulatory requirements.




Support customer audits and ensure documentation readiness for GMP, regulatory, and customer compliance standards.
Maintain documentation in alignment with company SOPs and industry validation practices.

Preferred candidate profile

Diploma / B.E. in Mechanical Engineering or related discipline
Experience in validation documentation (DQ, IQ, OQ, PQ) in machinery, pharma equipment, or engineering manufacturing
Proficiency in Microsoft Office and document control systems
Solid technical writing skills, attention to detail, and communication ability

📌 Documentation Engineer Gujarat
🏢 SHREEJI FLOWTECH SYSTEMS
📍 Gujarat