QC 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 Quality Control, Data Integrity, and compliance in a pharmaceutical environment? Then, join our team as our new QC Compliance Officer, where you will support QC equipment validation and strengthen Data Integrity practices across the QC laboratory.

You will work closely with QC colleagues and cross-functional teams to ensure laboratory equipment, documentation, and processes comply with cGMP, requirements and company policies.

Based in Koropi, you will report to the QC Compliance Coordinator, with the flexibility to work from home based on mutual agreement and business needs.

HOW YOU’LL FIT IN:

• Coordinate validation activities for QC laboratory equipment and computerized systems.
• Support the implementation and continuous improvement Data Integrity practices within the QC laboratory.
• Prepare, issue and review QC documentation, SOPs, change controls, and compliance records.
• Support investigations, deviations, and troubleshooting activities.
• Provide guidance to QC analysts on validation and compliance topics.
• Contribute to audit readiness and continuous improvement of QC compliance.
  
  
  

YOU BRING:

• University degree in Chemistry, Pharmacy, Biology, Food Technology or another relevant discipline.
• At least 2 years of experience in a Quality Control laboratory.
• Fluency in Greek and good command of English.
• Strong knowledge of analytical laboratory equipment and instrumentation, with experience in validation activities considered an advantage.
• Good understanding of GMP/cGMP requirements and Data Integrity principles, with the ability to apply them in a laboratory environment.
• Confidence working with software and computerized quality systems; an IT or technology-related background is considered a strong advantage.
• Strong organizational, communication, and problem-solving skills.
• A collaborative mindset and ability to work effectively across 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.
  
  
  

What’s next?

Please submit your application before the 22nd of October 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 or face-to-face 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.