Level

AstraZeneca

Quality Assurance Assistant - 15 Month FTC - Budaors 

AstraZeneca is hiring a Quality Assurance Assistant - 15 Month FTC - Budaors  in Budapest, Hungary. Level rates it ; you can apply on Level.

Level's read on this job

  • Level rates this role Little AI ●○○○: aI is not part of the work.
  • Tools and skills the posting cites include quality assurance, compliance and documentation.
  • Level files it as a mid-level role.
  • Level lists 1,100+ other open roles at AstraZeneca.
  • The role was posted within the past two weeks.

AI in this role

Support quality operations and compliance in a warehouse environment through documentation, deviation management, and regulatory checks.

quality-assurancecompliancedocumentationdeviation-management

Quality Assurance Assistant - 15 Month FTC - Budaors 

 

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.

 

What you’ll do


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.

 

Key Responsibilities


·                  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


Your profile


·                  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

 

Preferred Qualifications


·                  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

 

Why AstraZeneca?


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.

How we rate this

Quality Assurance Assistant - 15 Month FTC - Budaors  at AstraZeneca rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Quality AssuranceComplianceDocumentationDeviation Management

Questions you could be asked

  1. Tell me about a project where quality assurance was part of your work. What did you do?
  2. Tell me about a project where compliance was part of your work. What did you do?
  3. Tell me about a project where documentation was part of your work. What did you do?
  4. Tell me about a project where deviation management was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Quality Assurance, Compliance, Documentation, and Deviation Management. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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