Job Description

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

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. This is a fantastic opportunity for an experienced professional who wants to be part of a truly innovative and revolutionary team!

To support our growing operations, we are looking for a CQV Officer to execute and coordinate commissioning, qualification, and validation activities for new equipment (manufacturing/ packaging), cleanrooms and utilities within a highly regulated environment. You will combine hands-on technical expertise with a strong coordination mindset, working closely with cross-functional teams and project leads.

We are looking for a proactive and solution-driven professional who takes ownership, acts with speed, and goes beyond task execution by identifying issues, validating them, and driving effective solutions.

This position reports to the CQV Coordinator and provides the flexibility of hybrif schedule working module.

YOUR KEY RESPONSIBILITIES

• Execute CQV activities for new equipment and systems in line with company standards.
• Perform and document commissioning and qualification/validation testing (FAT, SAT, DQ, RA, IQ, OQ, PQ, etc.) to verify that the equipment design and operation comply with the approved technical and user requirements specifications.
• Contribute to the preparation of the Annual Site Validation Master Plan (VMP).
• Perform periodic reviews of computerized systems to ensure continued compliance.
• Collaborate with project leads, Quality, Manufacturing, IT, and external partners.
• Support planning, tracking, and delivery of CQV project activities.
• Participate in the investigation of any events and deviations as the responsible person for assessing the potential impact on the validated state of a system.
• Contribute to audit preparation and participate in inspections when required.

WHAT YOU SHOULD BRING TO THE TEAM

• University equivalent diploma in Engineering, IT, Chemistry, Pharmaceutics or relevant science.
• At least 2 years of experience within an industrial environment, preferably in pharmaceutical or alternatively in process industry.
• Fluent in Greek and English.
• Strong analytical and technical oriented mindset.
• Proven project and time management skills.
• Effective communication and effective cross-functional collaboration.
• Customer-oriented, with strong decision-making skills.
  

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, 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) and extra benefits.
• 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 interview to get to know each other. We will keep you posted during the process!

Please note: this position will be posted until May 29th. We kindly ask you to submit your CV in English.

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.