AstraZeneca Posted November 10, 2026

Quality Assurance Assistant - 15 Month FTC - Budaors

Budapest, Hungary Full time
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AstraZeneca is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Budapest, Hungary
Employment type
Full time

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.

1502Comparable roles tracked
1357Currently active
147Companies hiring similar roles
54Countries represented

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.

This roleSubject Not listed on this posting
Lowest disclosed · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $123,250)

Where these roles are based

Top locations among the 1502 comparable roles

United States589
Ireland88
Germany72
China72
France67
India57

+ 48 more countries

Seniority mix

731 of 1502 peers have a known seniority level

Manager223
Senior189
Intern/Fellow/Postdoc98
Associate65
Director46
Associate Director45
Principal33
Senior Director25
Executive/VP7

Therapeutic area mix

3 of 1502 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2
Respiratory1

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.

40%similar
Mylan Hungary Kft. Komárom, Hungary Manager
Same function Same country
40%similar
Servier Budapest, Hungary
Same function Same country
40%similar
Teva Pharmaceuticals Debrecen, Hungary
Same function Same country
40%similar
Teva Pharmaceuticals Debrecen, Hungary
Same function Same country
40%similar
Servier Budapest, Hungary
Same function Same country
40%similar
GlaxoSmithKline Biologicals Kft. Hungary Gödöllő, Hungary
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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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.

40%
Qualified Person Manager (Határozott időre)
Mylan Hungary Kft. · Komárom, Hungary · Manager
Function Therapeutic area Seniority Country
40%
Éves Termékfelülvizsgáló
Teva Pharmaceuticals · Debrecen, Hungary · Seniority not listed
Function Therapeutic area Seniority Country
25%
Principal Scientist GMP Environmental Monitoring Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
25%
Sr R&D Quality Assurance Engineer F/M
AbbVie · Annecy, Auvergne-Rhône-Alpes · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.