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Quality Assurance (QA) Product Compliance Expert

WHO ARE WE?

 

ROPU MIDI is a Regional Operating Unit that covers all local Human Pharma and Animal Health Operating Units across Belgium, Denmark, Norway, Finland, Greece, Portugal, Sweden, and The Netherlands. MIDI has a multicultural and diverse work environment. More than 1.800 employees are striving to work together to improve lives for patients and animals in our region.

Boehringer Ingelheim's site in Koropi, Greece, is a vital facility dedicated to the production of high-quality pharmaceutical products. Established in a strategic location near Athens, the Koropi site has played a significant role in the company's global operations, focusing on manufacturing and distribution. Over the last year the facility is committed to innovation and excellence for human pharmaceuticals.  Boehringer Ingelheim Koropi upholds the highest standards of safety, quality, security and environmental stewardship, aligning with the company's global priorities.


THE OPPORTUNITY

We are seeking a QA Product Compliance Expert to support Quality Assurance activities related to product compliance coordination, ensuring alignment with GMP standards, registered documentation, and internal quality systems.

In this role, you will contribute to safeguarding product quality and compliance while supporting the QA Product Compliance Manager in maintaining high standards across systems, processes, and cross-functional collaboration. You will collaborate closely with key cross-functional stakeholders, including Supply Chain and Production, as well as various teams within the Quality Operations function.

This position is based in Koropi and reports directly to the Quality Assurance Product Compliance Manager, with flexibility of hybrid working module.

This is a fantastic opportunity for an experienced professional who wants to be part of a truly innovative and revolutionary team! Join us if you want to make the difference.

 

HOW YOU’LL FIT IN:

As QA Product Compliance Expert, you will:

  • Coordinate quality activities between different teams and contributors to ensure timely completion of product transfer activities, and continuous market supply.
  • Perform quality evaluations (OOX) and ensure compliance with internal procedures and regulatory standards.
  • Approve validation documentation (PPQ, protocols, reports, risk assessments, control strategies) in collaboration with Production department and sub-teams.
  • Support SOP improvements and contribute to continuous quality system enhancements.
  • Provide quality oversight for the introduction of New Chemical Entities to the Koropi site.

 

 

YOU BRING:

  • Bachelor’s/ Master’s degree in Chemistry, Pharmacy, Food Technology, or another relevant scientific discipline.
  • Minimum of 2 years’ experience in the pharmaceutical industry, preferably in Quality or Production.
  • Native Greek speaker and excellent command of English language.
  • Experience with SAP or/and other computerized systems (e.g., Trackwise, GoTrack).
  • Strong knowledge of GMP/GxP standards and pharmaceutical quality systems.
  • Customer-focused and solution-oriented, with a proactive approach to simplifying complex processes.
  • Solid decision-making skills, self-driven, and able to collaborate effectively across local and global teams.


WHAT WILL YOU GET IN RETURN?

Next to the opportunity to develop and challenge yourself while learning from a fast-paced environment: 

  • Work in a wellbeing-oriented organization (Premium access to Headspace and ongoing support and initiatives related to ways of working to help our employees to stay healthy and constantly improve physical, emotional, mental, and spiritual well-being) 
  • Customized Development plan based on your role and aspirations, and access to international development opportunities and languages + training programs 
  • Competitive salary (plus annual bonus, participation in company life insurance and private healthcare program) and extra benefits.
  • A fun and diverse working environment. 

 

Please note that pay information will be shared during the recruitment process.


What’s next?

Please submit your application before the 30th of June 2026. We will have a look at your CV and cover letter. If we see a match, we will invite you for a video call interview to get to know each other. We will keep you posted during the process!

 

Screening:

In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (“SPL”). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.

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