Experience: 3–6 Years
Qualification: Diploma / Bachelor’s in Mechanical / Production Engineering
Job Summary
Responsible for preparation, review, and control of technical documentation for pharmaceutical machinery, ensuring compliance with GA drawings, URS, work orders, and technical specifications.
Key Responsibilities
- Prepare & verify DQ, FAT, IQ, OQ documents, manuals, and certificates
- Ensure documentation alignment with GA drawings, URS & work orders
- Maintain machine serial numbers and document control records
- Coordinate with customers for approvals and documentation queries
- Maintain calibration records & instrument certificates
- Support QC during FAT activities
- Assist service team with documentation-related support
Required Skills
- Knowledge of pharma equipment documentation (DQ, IQ, OQ, FAT)
- Understanding of GMP & regulatory requirements
- Good coordination and communication skills
- Strong attention to detail and documentation accuracy
Preferred
- Experience in pharmaceutical machinery industry
- Exposure to validation and audit documentation
HR Sushamita – 7066153147
Pay: ₹30,000.00 - ₹35,000.00 per month
Work Location: In person
