Work as Specialist Quality Operations at Novartis

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
Provide Quality Service in compliance with cGMP regulatory requirements and the Novartis Pharma Quality Manual and Policies by implementing processes, systems and tools that realize the Quality Operations services across Novartis divisions.

Key Responsibilities:
• Prepare Regulatory Statements/declarations, Quality Assurance Agreement, Quality Risk Assessment for excipients, Regular Material-/Supplier-Monitoring and packaging material as per agreed tasks with the customers.
• Perform and deliver Quality Operations services in support of product quality compliance and regulatory workflows
• Hold accounts in workflow applications (like SAP, Dragon, SUBWAY, TEDI etc.) to ensure appropriate execution of service deliverables
• Escalate service related GxP and non-GxP issues and ensure timely investigation and compliance with local and global operating procedures.
• Ensure compliance to the Novartis internal quality standards, relevant regulatory requirements, filed product quality standards and service level agreements.
• Support implementing service quality and process improvement projects, CAPA management within Quality Service Centers.
• Comply with all internal functional operating procedures like time tracking, KPI reporting, ticket management tools and other internal systems and processes.

Candidate Profile
• M.Pharm / MBA / Engineering/equivalent from a reputed institute.
• Min 3 yr Experience in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances/ products/Medical device.
• GxP-knowledge, Broad IT-knowledge
• Fluent in English (written and spoken)
• Good communication, presentation and interpersonal skills. Experience of working closely with the global stakeholders

Additional Information
Experience : 3 years
Qualification : M.Pharm / MBA
Location : Hyderabad, AP
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality
End Date : 30th September, 2021