Job Purpose
To support and execute qualification and validation activities related to production equipment, utilities, and processes in an Oral Solid Dosage (OSD) manufacturing facility, ensuring compliance with USFDA, cGMP, and regulatory requirements.

Key Responsibilities
Qualification & Validation Activities
Execute and support qualification of:
Equipment (DQ, IQ, OQ, PQ)
Utilities (HVAC, purified water, compressed air, etc.)
Production areas and systems
Perform process validation activities for OSD products including:
Prospective, concurrent, and re‑validation studies
Prepare, review, and execute validation protocols and reports as per approved SOPs.
Ensure validation activities are completed within defined timelines.

Production Support
Coordinate with Production, Engineering, QA, and QC teams during qualification and validation activities.
Support scale‑up, technology transfer, and recent product introduction from a validation perspective.
Ensure adherence to approved BMRs, SOPs, and validation protocols during execution.




Assist in troubleshooting process or equipment‑related issues during validation batches.

Documentation & Compliance
Prepare and maintain validation documentation in compliance with:
USFDA
cGMP
ICH guidelines (Q8, Q9, Q10)
Ensure data integrity and compliance with ALCOA+ principles.
Maintain proper documentation, logs, and records for audits and inspections.
Support regulatory inspections, internal audits, and customer audits related to validation.

Continuous Improvement
Participate in risk assessments (FMEA, risk analysis) related to validation activities.
Support change control evaluations and impact assessments.
Contribute to continuous improvement initiatives in production and validation processes.

Educational Qualification
Bachelor’s degree in:
Pharmacy (B.Pharm / M.Pharm)

Experience
6–8 years of experience in:
Production / Qualification / Validation
USFDA‑approved OSD pharmaceutical

📌 Senior Executive Daman
🏢 SUN PHARMA
📍 Daman