Do you have expertise in Quality Assurance and a passion to play a critical role as the eyes and ears of our patients? If you have the passion and the drive to accelerate growth and make people's lives better - then AstraZeneca is the place for you._**ABOUT ASTRAZENECA**AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation 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.At AstraZeneca, we unlock the power of what science can do. Empowered to explore, everyday we work towards our ultimate aim - treating, preventing, modifying and even curing complex diseases.**BUSINESS AREA**In Quality, our work is important and valued. An unrivalled forward-looking mindset, there's no better place to work at the forefront and learn how to add real value to a business throughout the lifecycle of our products - discovery, development and commercialisation.As the voice of the patient, every batch we certify is a personal stamp of approval. Not something we take lightly, we are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes.**What you'll do**Provides Quality Assurance support to an assigned area. Non-supervisory, provides advice in areas of processes and procedures. Role holder ensures efficient processes and procedures are maintained within the boundaries of regulatory compliance for relevant GxP.**General Accountabilities**:**Typical Accountabilities**:- Perform batch review before batch disposition by QA Qualified Person- Aligning QA work schedule to consistently provide and supply high quality product.- Ensuring the implementation of update Quality Management System applicable to QA operations, including in developing and maintaining SOP/Work Instruction in QA area- Managing implementation of GMP Training Management i.e ensuring Job Description and Personnel Qualification Training program and its documentation are in place and keep updated by each respective line manager- Managing Document Control, Document Retention and Archival- Develop and managing Product Quality Review (Annual Product Review) Program & Report- Managing communication with Global Stability team in developing and maintaining Site Stability Program- Participate in problem solving or specific issues to ensure GMP and regulatory compliance, i.e in any site deviation, supplier deviation/material complaint- Provide Quality review and assessment as QA Subject Master Expert in Change Management and Risk Management- Support in managing CAPA of Internal & External Audit- Perform continuous improvement and work as part of the Regional and Global Quality network to share best practice and standardize ways of working.**Essential for the role**- Bachelor's degree of Pharmacy and having Apothecary degree- Having experience in Pharmaceutical company in QA or QC activities- Familiar with quality system and implementation of GMP and SHE- Excellent communication skill- Good Analytical skill and knowledge- Fluent in English, minimum passive- Computer literate**Why join Operations at AstraZeneca?**We are driven by our commitment to deliver accelerated growth for AstraZeneca and to make people's lives better. It pushes us to keep building on our foundations and progressing as we turn our ever-growing and increasingly complex pipeline from molecule to medicine. Be part of evolving how we work with Lean, cutting-edge science, digitalisation and sustainable practices.**So, what's next?**- Are you already imagining yourself joining our team? Good, because we can't wait to hear from you.- Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it's yours.**Where can I find out more?**Our Social Media, Follow AstraZeneca on LinkedInFollow AstraZeneca on FacebookFollow AstraZeneca on InstagramIf you have site, country or departmental social media then feel free to switch any of the above links.
