Expert, Process Technology & Transfers (PT&T)

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

As an Expert in Process Technology & Transfers (PT&T ), you will provide technical expertise in pharmaceutical production processes, with a particular focus on Cleaning Validation and Cleaning Process Lifecycle Management , ensuring scientifically sound, compliant, and robust process performance throughout the commercial lifecycle. You will act as a subject matter expert, supporting technical troubleshooting, decision-making, and continuous improvement initiatives, and you may lead projects of low complexity at a functional level.

This position is based in Koropi and you will report to the Senior Expert Process Technology & Transfers.

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 has been 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.

This is a fantastic opportunity for a technically minded professional who wants to make a tangible impact on product quality, patient safety, and supply continuity.

YOUR KEY RESPONSIBILITIES

- Act as subject matter expert for assigned processes, technologies, or Cleaning validation areas, and contribute to the relevant MSO systems within Process Technology & Transfers (PT&T).

- Design, plan, execute, and evaluate cleaning validation and lifecycle activities, including monitoring data analysis and risk-based assessments.

- Create, review, and update cGMP‑compliant cleaning validation documentation, including validation protocols, reports, and supporting documents.

- Support the creation, assessment, and documentation of deviations and investigations, including root cause analyses and corrective and preventive actions.

- Support inspections, audits, and regulatory interactions as a technical expert, maintaining permanent inspection readiness.

- Contribute expert input to technology transfers, product and process changes, and the introduction of new materials or technologies, as well as OPEX development; act as a (Transfer) Lifecycle Project Team Member when assigned.

- Collaborate closely with Production, Quality, and other relevant areas to ensure smooth execution of validation activities, proactively identifying and escalating issues, deviations, or bottlenecks.

WHAT YOU SHOULD BRING TO THE TEAM

- Bachelor’s degree in Chemistry, Biology, Agriculture, Process Engineering, Pharmacology, or a related scientific discipline.

- Minimum 1 year of experience in a pharmaceutical or regulated environment, preferably in Production and/or Quality.

- Good understanding of GMP principles and pharmaceutical quality requirements.

- Ability to work effectively in a cross‑functional environment, with good planning and decision‑making skills.

- Fluency in Greek and English.

- Customer‑oriented mindset with a proactive and solution‑focused approach.

- Strong communication and time management skills, with attention to detail and documentation quality.

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).

- A fun and diverse working environment.

We kindly ask you to submit your CV in English.

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 November 24th and we only accept applications 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.