Seeking Quality Specialist (3-5 Yrs) for Cipla Limited

Role Summary: We are looking for an experienced Quality Specialist with 3-5 years of experience to join our team at Cipla Limited in Nasik. The ideal candidate will possess a BBA/BBM degree and a strong understanding of quality management systems within the pharmaceutical industry. This role is crucial for ensuring compliance with regulatory standards and driving continuous improvement in our quality processes.

Key Responsibilities:
- Monitor and implement quality control procedures to ensure product consistency and adherence to specifications.
- Participate in internal and external audits, ensuring readiness and addressing any non-conformities.
- Review and approve quality-related documentation, including batch records, SOPs, and validation reports.
- Collaborate with cross-functional teams (Production, R&D, Regulatory Affairs) to resolve quality issues and implement corrective and preventive actions (CAPA).
- Analyze quality data and trends to identify areas for process improvement and risk mitigation.
- Stay updated with relevant regulatory guidelines and industry best practices.
- Assist in the development and execution of quality training programs for staff.
- Contribute to the maintenance and improvement of the Quality Management System (QMS).