Senior Quality Specialist External Quality - Responsible Person (Budapest)
About this role
Senior Quality Specialist External Quality - Responsible Person (Budapest)
Diverse Minds. Bold Disruptors. Meaningful Impact.
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
We are seeking a qualified and experienced
Senior Quality Specialist External Quality -
Responsible Person
to join AstraZeneca’s pharmaceutical wholesale operations in Hungary. This role is critical in ensuring compliance with GDP requirements, safeguarding product quality, and enabling the safe release of medicinal products to market.
The successful candidate will act as a key quality authority, working closely with internal teams, regional stakeholders, and regulatory bodies.
Responsibilities
- Quality Certification & Product Release
- Review, assess, and certify incoming medicinal products and associated documentation
- Release products for sale (placement into saleable stock) for domestic and regional markets
- Block products where necessary in case of quality concerns
- Inbound & Warehouse Quality Oversight
- Be present onsite during receipt of medicinal product shipments
- Oversee goods receipt, sampling, and organoleptic inspection
- Ensure segregation of damaged goods
- Monitor compliance with approved procedures
- Storage & Distribution Compliance
- Ensure adherence to storage and transportation conditions as defined in marketing authorisations
- Oversee both:
- Ambient products
- Temperature-controlled (cold chain) products
- Quality Assurance Activities
- Manage product complaints and quality defect reporting
- Support product recalls (as Deputy Recall Administrator, if assigned)
- Investigate deviations and implement corrective actions
- Review, update, and approve SOPs
- Conduct self-inspections and internal audits
- Participate in external and third-party audits (e.g. manufacturers, logistics providers, wholesalers)
- Training
- Deliver training in line with the approved training plan to:
- Internal QA staff
- Warehouse and logistics personnel
- Stakeholder Management
- Maintain close collaboration with:
- Regulatory Affairs
- Logistics and Finance teams
- Marketing and Business Units
- Regional regulatory and logistics partners
- Wholesalers and external partners
- Regulatory authorities
- Regulatory & Compliance
- Ensure all activities comply with:
- Hungarian and EU legislation
- GDP/GMP requirements
- EFPIA and AIFP Codes of Practice
- Support pharmacovigilance obligations, including timely reporting of safety information
- Qualifications & Experience
Requirements
- Degree in
- Pharmacy
- (Certified Pharmacist)
- Minimum
- 1 year experience as a Responsible Person
- Strong understanding of GDP requirements
- Experience in pharmaceutical quality systems (QA, GMP/GDP)
- Fluent English (professional / negotiation level)
- Valid driving licence
Nice to have
- 1–5 years’ experience in GDP environment
- Experience in GMP
- Why Join AstraZeneca?
- Work in a highly regulated, high-impact quality role
- Be part of a global, science-led biopharmaceutical company
- Contribute to ensuring the safety and quality of medicines for patients
- Collaborate with international and cross-functional teams
- Date Posted
- 03-Jun-2026
- Closing Date
- 29-Jun-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.