QMS Officer at Cipla

Job Purpose:

• QA Process optimization and simplification of systems and reporting.
• Facilitate Quality Assurance (QA) software implementation and cross functional integration.
• Developing, implementing, and maintaining QA Business Intelligence and reporting platforms, and continuous improvement thereof to aim/move towards real time reporting.
• Project Management / SPOC function for SAGA region for QA software roll out.
• To review non-conformance reports, deviation requests and subsequent correspondence thereof, and drive these to timeous closure.

Key Accountabilities:

• QA Process Optimization and Efficiency
• QA Reporting
• IT Solutions
• Review approval of Non-conformances (NC), Deviations and Out of Specification/Trend (OOS/OOT) notifications
• Supports the Effective Implementation and Management of the Quality Management System (QMS)
• Projects, General Administration and Support
• Pharmacovigilance

Skills & Knowledge:

Qualification:

• Bachelor’s degree in a science or technology field (B.Sc/ B.Tech), or other relevant qualification e.g. Diploma in Quality Management

Experience:

• At least 5 years’ work experience in Quality Assurance, preferably in a pharmaceutical company or similar background

Skills:

• Computer skills – MS Word, MS Excel at advanced/intermediate level.
• Ability to navigate unassisted through QMS SharePoint systems and databases.