Experience: 3–6 Years
Qualification: Diploma / Bachelor's Degree in Mechanical Engineering or Production Engineering
Key Responsibilities
- Prepare and maintain DQ, IQ, OQ, FAT documents, manuals, and certificates.
- Ensure documentation compliance with technical specifications and customer requirements.
- Coordinate with customers regarding documentation approvals and queries.
- Maintain document control, revision records, and calibration documentation.
- Support QC and service teams in FAT and documentation-related activities.
Required Skills
- Knowledge of pharma equipment documentation (DQ, IQ, OQ, FAT).
- Understanding of GMP and regulatory requirements.
- Strong documentation, coordination, and communication skills.
- Attention to detail and documentation accuracy.
Preferred Candidate
- Experience in pharmaceutical machinery industry.
- Exposure to validation and audit documentation.
Contact
HR – Sushamita 7066153147
Pay: ₹30,000.00 - ₹40,000.00 per month
Work Location: In person
