QC Support Analyst

Join Us As A Quality Control Support Analyst

As a new team member, your role will involve participating in CDMO/CMO projects within Quality Control, maintaining contact with partners, and supporting QC-related validation and transfer activities. Your duties will include performing, overseeing, and ensuring QC processes within and across organizations.

You will also be responsible for completing compliance tasks related to quality control, preparing relevant documentation, and generating status reports.

The following tasks await you if you thrive in a dynamic environment:

• Performing and supporting QC analytical tasks in CDMO and CMO projects
• Creating plans and protocols for analytical method validations and conducting laboratory measurements
• Preparing transfer protocols, reports, and related documentation, and tracking related lab and other tasks
• Conducting regular reviews of analytical methods and participating in annual validation plans
• Documenting and participating in state-of-the-art validation activities, supporting laboratory tasks
• Evaluating compliance with new regulatory requests, coordinating tasks, and supporting lab measurements
• Performing drug master file follow-up tasks
• Overseeing calibration/qualification measurements of lab equipment/systems
• Ensuring adherence to company policies, procedures, and standards during development and user support
• Maintaining contact with colleagues in related organizations for task completion
• Initiating change procedures and providing expert opinions
• Maintaining statistical records
• Conducting risk analyses
• Creating, verifying, querying, and maintaining LIMS master data
• Drafting quality specifications, preparing instructions for machine operation, tracking changes, and documenting them
• Managing procurement and disposal processes for instruments and equipment, documenting and verifying them
• Participating in planning, ensuring, monitoring, and controlling annual goals
• Preparing for and participating in inspections/audits
• Maintaining internal policies and procedures, ensuring regulatory compliance, and protecting company assets
• Assessing risk parameters in your area of responsibility and implementing preventive measures if necessary
• Participating in archival and inventory documentation processes

We welcome your application if you meet the following criteria:

• Higher education in IT or analytics (chemist/chem engineer/analyst)
• Two years of experience with IS/IT analytical software
• Knowledge of at least one IS/IT application/area and a functional area
• Intermediate English proficiency, both written and spoken
• Problem-solving, decision-making, and team-oriented skills
• Good communication skills
• Ability to work flexibly, focusing on key tasks, and adapting to changing priorities
• Basic computer skills (Word, Excel, PowerPoint)
• Confident communication skills in English (both written and spoken)

What We Offer:

• Professional development opportunities with diverse technologies
• Varied tasks aimed at process optimization that require creativity
• Independent work with continuous feedback and performance reviews
• Work in a pharmaceutical raw material and intermediate manufacturing site in a regulated, clean environment
• Competitive base salary and benefits package
• Gross annual salary of 636,000 Ft based on the company’s cafeteria plan (even during probation)
• Annual basic health screening and ongoing outpatient care at the Buda Health Center, with one paid day off
• Discounted sports facilities (sauna, gym)
• Group life and accident insurance
• Voluntary pension fund membership
• Free parking

Why Join Us?

• We are looking for a long-term team member in a dynamic team where we grow together, respect, and inspire each other.
• We offer continuous development opportunities:
  We don’t know what career path you want to pursue, but we are confident that you will find your way with us in an exciting role, an opportunity for growth, and skill acquisition in a global company and in a pharmaceutical quality environment.

Work location:

Budapest, IV. district

Learn more about this opportunity and apply today!

About the Company:

EUROAPI Hungary Kft. is a unique active pharmaceutical ingredient (API) manufacturing company, a subsidiary of the French-based EUROAPI. The independently listed company on the French stock exchange combines API production, trade, and development activities across five European countries through its network of API manufacturing sites. The products manufactured here are sold in 80 countries.

Our Budapest site is a pharmaceutical ingredient manufacturer with excellent expertise in both chemical development and production. It produces over 40 different raw materials using the latest technologies and has been the world’s leading generic prostaglandin producer since 2000. The development of the prostaglandin model is a unique professional innovation of the site, resulting from our commitment to local expertise and development.