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Production 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.

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

Are you passionate about compliance within pharmaceutical production processes? We are recruiting for a Production Compliance Officer – a unique development opportunity in a truly innovative and revolutionary team! At Boehringer Ingelheim, you'll always be supported to create a career that's challenging and rewarding.

In this role, you implement and establish continuous improvement of the quality systems related to Production, while ensuring that Good Manufacturing & Packaging practices together with EHS & Quality standards are followed.

This position is based in Koropi (Greece) and reports directly to the Production Systems & Compliance Manager, with flexibility of hybrid working module.

 

YOUR KEY RESPONSIBILITIES:

  • Conduct process mapping and drive continuous improvement initiatives within assigned areas, using tools such as GAP analysis, SOPs, and personnel training.
  • Review manufacturing and packaging documents to ensure they meet compliance requirements.
  • Handle daily compliance activities for Manufacturing and Packaging Departments, including follow-up on CAPAs, change controls, deviations/investigations, and training coordination.
  • Oversee and administer the LOS training management system for the relevant areas of responsibility.
  • Actively support and participate in GMP audits within manufacturing and packaging

 

YOU BRING:

  • Bachelor’s/ Master’s degree in Engineering, Science or another relevant scientific discipline.
  • 1- 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., MES).
  • Good understanding of GMP standards and regulatory requirements.
  • Customer-focused, compliance-minded, and able to collaborate effectively in a cross-functional 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 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 9th of July 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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