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

- AutoCAD proficiency

- SOP development

- Testing methodologies (FAT, SAT, DQ, IQ, OQ, PQ)

- Strong communication skills

Pay: ₹50,000.00 - ₹62,000.00 per month

Advantages:

- Paid sick time
- Provident Fund

Work Location: In person

📌 Documentation Executive - Borivali (India)
🏢 Quick Jobs Placement
📍 India