Quality Assurance/Regulatory Compliance Officer

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.

THE OPPORTUNITY

Are you ready to ensure global compliance and support the worldwide availability of life-saving medicines?

As a QA Regulatory Compliance Officer, you will play a vital role in maintaining regulatory compliance. You’ll work at the intersection of quality, compliance, and global regulatory standards—ensuring that our products meet the highest expectations of health authorities worldwide.

This is a dynamic role that requires strong coordination, critical thinking, and the ability to navigate complex international regulatory environments. You’ll collaborate with cross-functional teams and contribute directly to the continuity of global supply and plant operations.

This position is based in Greece, Koropi. 

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. 

YOUR KEY RESPONSIBILITIES

• Prepare CMC documentation and ensure compliance with global regulatory standards across 100+ markets.
• Collaborate with Global and Local Regulatory Affairs, Corporate QA, Supply Chain, Legal, and other internal stakeholders.
• Participate in cross-departmental meetings and provide regulatory input as needed.
• Support global product launches, transfers, and dossier submissions.
• Maintain effective communication with local regulatory authorities, overcoming cultural and procedural differences.
• Ensure that all activities align with internal quality systems and external regulatory expectations.

Please note: this position will be posted until the 18th of July, and we only accept applications in English.

WHAT YOU SHOULD BRING TO THE TEAM

• A diploma degree in Chemistry, Chemical Engineering or other related field
• At least 2 years of experience in a pharmaceutical quality environment.
• Strong organizational skills and the ability to manage multiple priorities under tight deadlines.
• A critical thinker with a strong sense of urgency and attention to detail.
• Experience with SAP and/or other quality systems (e.g. TrackWise).
• Excellent communication skills and the ability to work effectively in a global, cross-cultural environment.

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 the physical, emotional, mental, and spiritual well-being). 
• Customized Development plan based on your role and aspirations, with several learning platforms such as LinkedIn Learning Premium, and access to international development opportunities and languages + training programs. 
• Competitive salary (plus annual bonus, participation in company life insurance and private healthcare program). 
• A fun and diverse working environment. 

What’s next?

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!

If you have any questions related to the recruitment process, please do not hesitate to contact Talent Acquisition MIDI: TalentAcquisitionMIDI.EU@boehringer-ingelheim.com 

DIVERSITY & INCLUSION

At Boehringer Ingelheim we share the opinion that diversity and inclusion is essential for the growth of our business and that our strengths and competitive advantage are also the result of the diversity of our company – diversity across the three dimensions of inclusion: Gender, Geography and Generation. Our people are part of a deep-rooted, family company philosophy that welcomes everyone! We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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.