Quality Assurance Assistant - 15 Month FTC - Budaors
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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
10-Nov-2026
Closing Date
19-Nov-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.
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1502 comparable Quality roles across 147 biopharma companies.
Salary context
261 of 1502 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1502 comparable roles
+ 48 more countries
Seniority mix
731 of 1502 peers have a known seniority level
Therapeutic area mix
3 of 1502 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.