AstraZeneca Quality Assurance Associate Vacancy 2021 – Apply Online
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Check out all the details on the same below:
Job Title: Associate – Quality Assurance
Location: India – Yelahanka
Key Duties and Accountabilities
- Ensure that cGMP’s requirements are adhered to as per Schedule M and AstraZeneca QCM.
- Documentation control includes maintenance of archival System by RMA tool.
Issuance, control, and maintenance of Standard Operating Procedure, Work instruction, and Formats through Aztec System. - KPI trending compilation and updation to Global Portal.
- Support the preparation and execution of internal and external audits and inspections.
- Support in implementation of improvement plan identified through the investigation.
- Awareness on lean culture, drive improvements and process simplification and lead or participate on interdepartmental Projects as required.
- Knowledge in SAP on Quality Module.
- Support the management of Quality Management System
- Knowledge in the Risk management system and deviation investigation.
- Reference sample management.
Eligibility Criteria
- Master’s in science / Pharmacy Graduate 3 to 6 Years experience in Pharmaceutical Quality Assurance.
- Conversant with Good Manufacturing Practice (cGMP) & QMS
- Fluency in computer systems including Microsoft applications, Essential SAP Knowledge.
Desirable for the role
Communication Skill.
- Knowledge in Tablet Manufacturing Process & Shopfloor QA
- Basic of SHE and Lean
- Knowledge in QC testing and review.
What you’ll do
This role Supports QA Manager to establish and sustain the culture of regulatory compliance at the India site and contributes to the QA function in executing and developing a quality management system and supports the site’s improvement. Knowledge of the Schedule M requirement and AZ QCM standards is essential.
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