Job Responsibilities:
- Document pharmaceutical process equipment such as PSG, MCD, PW/WFI systems, and sterile process vessels.
- Develop and document essential SOPs related to equipment testing.
- Understand and apply pharma validation processes for respective equipment.
- Ensure compliance with 21 CFR Part 11.
- Create and maintain QC documentation for project execution.
- Interpret P&ID, GA drawings, and electrical automation drawings.
- Conduct FAT, SAT, DQ, IQ, OQ, and PQ testing.
- Collaborate with engineering teams on documentation requirements.
- Utilize AutoCAD for documentation purposes.
- Maintain quality standards throughout documentation processes.
Required Skills:
- Documentation of pharmaceutical equipment
- Knowledge of QC processes
- Pharma validation processes
- PLC / HMI / IPC - SCADA documentation
- Understanding of P&ID and GA drawings
- Testing methodologies (FAT, SAT, DQ, IQ, OQ, PQ)
- Strong communication skills
Pay: ₹50,000.00 - ₹62,000.00 per month
Benefits:
- Paid sick time
- Provident Fund
Work Location: In person
