IPQA Chemist

Experience Required: Min 5 Years

Key Responsibilities:

• In-Process Quality Assurance:
• Perform in-process checks during manufacturing, including line clearance, dispensing, granulation, compression, coating, and packaging.
• Monitor critical control points and ensure compliance with batch manufacturing records (BMR) and batch packing records (BPR).
• Documentation and Compliance:
• Review and verify BMR and BPR for accuracy and completeness.
• Maintain and update quality documentation in accordance with GMP and regulatory requirements.
• Analytical Testing:
• Conduct analytical tests on raw materials, in-process samples, and finished products to ensure quality standards are met.
• Utilize instruments such as disintegration apparatus and friability testers for routine checks.
• Deviation Management:
• Identify, document, and investigate deviations or non-conformances during the manufacturing process.
• Implement corrective and preventive actions (CAPA) to address identified issues.
• Training and Support:
• Provide training to production staff on GMP, SOPs, and quality assurance procedures.
• Assist in internal and external audits, ensuring readiness and compliance.
• Continuous Improvement:
• Participate in continuous improvement initiatives to enhance product quality and process efficiency.
• Collaborate with cross-functional teams to resolve quality-related issues.