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Work as Quality Operations Specialist at Novartis

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Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post : Specialist - Quality Operations

Job Description
Use the GxP experience and the well-established knowledge of Quality Management System and the relevant International Legislation in daily role. Contribute to the operational business in compliance with cGMP regulatory requirements and the Novartis Pharma Quality Manual and Policies. Support PLS delivery by implementing processes, systems and tools that realize the Quality Operations services across Novartis divisions. Support the successful implementation of the NBS vision and strategy and the Novartis Quality strategy within PLS-M&SO organization.
• Perform Product Quality service operations like technical complaints, technical deviations, product change requests, product release, supplier qualification, product quality review, artworks, GxP documentation, audit support and application user support within PLS-M&SO.
• Hold and manage key accounts in workflow applications to ensure appropriate execution of service deliverables.
• Generate and analyze predefined and ad-hoc reports in various applications (like AGILE PLM, AQWA etc.) and perform follow-up actions if required.
• Ensure compliance to the Novartis internal quality standards, relevant regulatory requirements, filed product quality standards and service level agreements.
• Create and review GxP documents including trend reports, qualification reports and technical investigations.
• Regularly communicate with customers and partners to collect feedbacks on support services, report deliverable and acquire process knowledge.
• Support implementing service quality improvement projects within PLS M&SO organization.
• Adherence to the service KPI’s and ensuring the service dashboard, order management framework and time sheet is always kept updated.

Candidate Profile
• University or academic degree in Chemistry, Microbiology, Biotechnology, Pharmacy or equivalent in English
• Experience in chemical/pharmaceutical industry.
• Min. 4-7 yrs Experience in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances or products.

Additional Information
Experience : 4-7 years
Qualification :
B.Pharm, M.Sc, B.Sc, M.Pharm
Location : Hyderabad, AP
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Technical Operations
End Date : 10th March, 2020


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