Roles & Responsibilities:
Ensure proper operation and cleaning of equipment and manufacturing areas related to Granulation, Compression, Coating, and Capsule Filling processes.
Handle Change Control, Deviation, Incident, and Market Complaint activities in compliance with company procedures and regulatory guidelines.
Maintain sound knowledge and implementation of Positive Manufacturing Practices (GMP) and Positive Documentation Practices (GDP) across manufacturing activities.
Prepare and review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and relevant Standard Operating Procedures (SOPs).
Participate in equipment and area qualification and ensure validation activities are conducted as per approved protocols and GMP standards.




Support in maintaining documentation for validation, qualification, and other manufacturing compliance records.
Coordinate with cross-functional teams to ensure smooth manufacturing operations and compliance with regulatory requirements.

Desired Candidate Profile:
Qualification: B. Pharma
Experience: 3 to 5 years of relevant experience in a similar role within a pharmaceutical formulation unit.
Robust understanding of OSD manufacturing processes, GMP, and GDP.
Good documentation, communication, and coordination skills.

📌 Qa Stability Executive Una (India)
🏢 Stanford Laboratories
📍 India