Interim Release QP Manager

Our partner is a global healthcare and pharmaceutical company working in a highly regulated manufacturing environment. You will lead the Qualified Person (QP) function, certifying products for release to EU and EEA markets and keeping operations compliant with GMP and Annex 16.

You will support regulatory inspections, manage quality risks and provide professional leadership to the QP team.

• Leading and coordinating QP activities and certifying finished products for EU and EEA release
• Reviewing batch documentation, deviations, investigations and Product Quality Reviews
• Reviewing and approving Technical Quality Agreements and supporting supplier audits
• Supporting regulatory inspections, internal audits and change control
• Managing quality complaints and recalls, and mentoring colleagues on GMP

• A degree in Pharmacy, Chemistry, Biology or a related science
• At least 5 years in the pharmaceutical industry
• Valid Qualified Person certification or authorisation
• Extensive knowledge of GMP, quality systems and regulatory inspections
• Fluent Hungarian and English (C1), plus previous leadership experience

• Competitive salary, annual performance bonus and a flexible cafeteria package
• Daily hot meal on site, commuting support and free shuttle buses from locations in Hungary and Slovakia
• Housing support for relocation and company car eligibility depending on the role
• Private medical services, insurance and health and wellness programmes
• Free English training and long-term development