- 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 Good Manufacturing Practices (GMP) and Good 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.