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.
It’s our patients that come first, every decision we make and action we take is centered around how we can better respond to their evolving needs, as well as those of healthcare professionals and partners. It’s why we are shaping patient care for the future, working along the whole experience to give hope to billions of lives across the world.
задачи
As a Quality Assurance Assistant, you will play a key role in supporting the quality operations of our Hungarian warehouse and ensuring compliance with national and global standards. You will work closely with colleagues in Hungary and across international teams to secure accurate documentation, smooth product flows, and timely handling of regulatory requirements. In this position, you will contribute to maintaining high-quality standards across our supply chain, actively participate in issue resolution and product handling, and support continuous improvements within the Quality function.
This is a fully on‑site role based in Budaörs, offering the chance to work closely with the team and be directly involved in daily quality operations. The position is a fixed‑term contract of approximately 12 months, providing a great opportunity to gain experience in a regulated, international environment.
Perform quality checks and manage documentation for domestic and regional products arriving at the warehouse
Prepare documentation required for product release activities managed by the Responsible Person
Compile required documentation to the Hungarian Health Authority
Manage permissions (e.g., “final sample,” “special permission”) issued by the Hungarian Health Authority and communicate relevant updates to the Regulatory Team
Execute core quality processes, including deviation management and complaint management
Support quality and process improvement initiatives
Conduct timely data entry and maintain documentation, including contributing to data analysis and report preparation
Coordinate market-specific documentation and maintain updated product, partner, and related lists
Actively participate in handling returned goods
Support the management of product complaints and complaint investigations
Carry out serialization flag checks and handle related issues
Participate in product rework activities
Collaborate and communicate effectively with both local Hungarian colleagues and international teams
требования
High school education with relevant experience, or a Bachelor's degree in Biology, Chemistry, Food Science, Engineering, or a related field
Demonstrated experience in working with established procedures and authorization controls
Native-level Hungarian skills (written and spoken)
Excellent verbal and written English skills
Experience working with compliance concepts such as GxP, SOPs, and SHE
Hands-on experience with quality management processes in a highly regulated environment
Experience using QA-related digital tools, documentation systems, and reporting platforms
Personal Attributes
Quick learner with strong ability to absorb new information
Responsible, reliable, and able to work independently
Comfortable handling complexity
Adaptable, resilient, and open to change
Precise, quality‑focused, and results‑driven
Strong communicator and effective team player
условия
At AstraZeneca, we’re dedicated to being a phenomenal Place to Work. You are empowered to push the boundaries of science and fuel your entrepreneurial spirit. There’s no better place to make a difference in medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and is always committed to lifelong learning, growth, and development. We’re on an exciting journey to pioneer the future of healthcare.
Date Posted
14-Oct-2026
Closing Date
30-Oct-2026
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
Входит в десятку крупнейших мировых фармацевтических компаний, которые занимаются научными исследованиями, производством и продвижением лекарственных средств, а также медицинским обеспечением
