Quality Assurance Assistant - 15 Month FTC - Budaors

Reposted 16 Days Ago
Be an Early Applicant
Budapest, HUN
In-Office
Entry level
Biotech • Pharmaceutical
The Role
Executes pharmaceutical quality processes, including deviation management, batch disposition recommendations, investigations, CAPA review, complaint handling, document approvals, GxP guidance, GMP training, regulatory documentation coordination, risk assessments, and quality metrics reporting. Works with internal quality, regulatory, operational excellence, vendors, and health authority inspectors in a highly regulated environment.
Summary Generated by Built In

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.

Skills Required

  • High school education with relevant experience, or an entry-level bachelor's degree in science or engineering, such as Pharmacy, Biology, or Chemistry
  • Experience with compliance management principles and concepts related to GxP, SOPs, and SHE requirements
  • Relevant experience executing quality management processes in a highly regulated environment
  • Experience using digital tools and applications for quality assurance reporting, documentation, and analysis

AstraZeneca Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.

  • Fair & Transparent Compensation — Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
  • Strong & Reliable Incentives — Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
  • Retirement Support — A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.

AstraZeneca Insights

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The Company
HQ: Gaithersburg, MD
70,000 Employees
Year Founded: 1999

What We Do

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.

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