Executive-QA Opportunity at Sun Pharmaceutical Industries Ltd: Ensuring Quality Excellence in Mohali – B. Pharma/ M. Pharma can apply

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Welcome to Sun Pharmaceutical Industries Ltd, where an exciting opportunity awaits in our Quality Assurance Department. We are currently seeking a dedicated Executive-QA with qualifications in B. Pharma/M. Pharma. This position is based in the vibrant city of Mohali. As an Executive-QA, you will play a pivotal role in ensuring our operations comply with global quality standards and cGMPs. Your responsibilities include implementing, operating, monitoring, and maintaining quality systems efficiently. You will be involved in the review and archival of quality system documents, actively participating in investigations and analysis for deviations, OOS, OOT, complaints, and audit findings. Additionally, your expertise will contribute to external audit preparations, management review meetings, and the management of CAPA efforts.
At Sun Pharmaceutical Industries Ltd, we value proactive individuals who can handle change management, CAPA management systems, and are adept at handling customer interactions during compliant investigations. Your role will also involve the preparation of APR/PQR, ensuring the highest quality standards in every aspect of our operations. Join us in this challenging and rewarding opportunity, where your skills will be essential in maintaining our commitment to quality and excellence in the pharmaceutical industry. #ExecutiveQA #QualityAssurance #PharmaceuticalIndustry #SunPharma #QualityStandards #CGMP #MohaliOpportunity

Name of the position

Executive- QA

Department

Quality Assurance

Qualification

B. Pharma/ M. Pharma

Location

Mohali

Company

Sun Pharmaceutical Industries Ltd

Job Responsibilities
1. Implement Operate monitor and maintain Quality Systems which enable operations on site to occur in an efficient manner and in compliance with Global Quality Standards and cGMPs.
2. Review and ARchival of Quality System Documents
3. Followup for timely closure of QMS docs
4. Participating in the investigations analysis for Deviations, OOS, OOT, Compliants and Audit finding, morevoer responsible for providing batch disposition as per the outcome of Deviation, OOS and OOT investigations
5. Supporting in external audits preparations and responding to audit findings
6. Compliation of the Internal Audit response and follow up
7. Assist in scheduling and preparation of management review meetings
8. Organize the CAPA meeting, coordinate amange CAPA efforts and interact with customers to conduct compliant investigations
9. Handling of Change Management & CAPA Management System
10. Assist to author, review and update quality procedures as applicable
11. Responsible for Handling of Complaints, Mock recall/ Recall and withdrawal of Drug Products
12. Retentions Sample Management
13. Preparations of APR / PQR

Post Date: 11th October 2023

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