LIMS PROJECT ENGINEER (H/F)

About Recipharm : Recipharm is a leading global pharmaceutical CDMO (Contract Development and Manufacturing Organization), committed to helping pharmaceutical companies navigate the complexities of product development and manufacturing since 1995. Our expertise spans the entire product lifecycle, from early development to commercial production, ensuring precision and reliability at every step. With a dynamic workforce of over 5,000 professionals across 8 countries, we support our partners with end-to-end services that span drug development, clinical trials, manufacturing, and commercialization. Our facilities are strategically located across France, Germany, India, Italy, Portugal, Spain, Sweden, and the US, with continued growth on the horizon. Location : This VIE position is based in Lisbon, Portugal (also possible in Leganes, Spain or Basel, Switzerland). You'll be joining a friendly and collaborative team at the Kaysersberg factory, where you'll gain valuable experience in pharmaceutical laboratory and IT applications critical to running these processes. About the mission : We are offering a VIE mission of at least 1 year, with the possibility to extend up to 2 years, within our Group Quality Management & Regulatory Affairs department. You will report directly to a Corporate Quality System Manager and play an essential role in supporting the global deployment project of a Laboratory Information Management System (LIMS) at 8 sites of the Group. You will be interacting with all local teams and, as such, working in a multi-cultural environment. The project spans laboratory processes and IT processes. Project-related tasks : • Participate to configuration workshops between Recipharm and the system vendor to setup the workflows in the Laboratory Information Management System (LIMS) • Define and create standard templates for data trending, labels and certificates in the system – as such lead a working group with all sites for alignment. • Coordinate all master data activities during the project between 8 sites involved • Create the global corporate procedure, instructions and training materials for end-users, ensuring clear and effective system usage. • Support the training management of users • Create the project validation package for sites for inspection readiness • Participate actively to the computerized system validation activities by executing test scripts • Learn the operational model of the e-quality system, gaining insight into how the system functions across the entire organization. Profile : We are looking for candidates who meet the following criteria: • Educational background: Degree in Pharmacy, Chemistry, Engineering, or a related field. • Fluency in English: Proficient written and spoken English is a must. • Communication skills: Excellent verbal and written communication skills with the ability to work well in a multicultural team. • Self-starter: Ability to work independently, manage priorities, and take initiative while remaining a team player. • Proficiency in MS Office: Strong skills in Excel and other MS Office applications. • Interest in Laboratory Systems: A passion for learning about electronic systems and IT solutions within the pharmaceutical industry. • Adaptability: Comfortable working in an international environment with diverse teams and stakeholders. Useful Information: Upon joining, you will receive a comprehensive welcome and onboarding program at our Kaysersberg factory, where you’ll be introduced to both your future manager and local mentors who will support you throughout your journey. This hands-on training will ensure you are fully prepared for your role within the team. At the site, you will be working in close collaboration with the local project Team (QC Manager and IT). Additionally, Recipharm will participate in your monthly rent for your VIE accommodation, subject to certain limitations. These details will be discussed with you during the interview process, ensuring transparency and clarity. This VIE leads to a perspective of a permanent position within Recipharm, at Kaysersberg or another site. Why to choose Recipharm : • Internal visibility: this project is strategic to the corporate quality roadmap and has strong attention from the senior leadership and executive committee. • International exposure: A unique opportunity to gain experience with a leading global player in the pharmaceutical industry. • Collaborative work environment: Work alongside passionate professionals in a welcoming, multicultural team. • Career development: Hands-on experience in a high-visibility strategic project, with the potential for long-term growth within Recipharm. We are committed to fostering a supportive environment where you can grow professionally and personally, while contributing to a transformative project with global impact

Profile : We are looking for candidates who meet the following criteria: • Educational background: Degree in Pharmacy, Chemistry, Engineering, or a related field. • Fluency in English: Proficient written and spoken English is a must. • Communication skills: Excellent verbal and written communication skills with the ability to work well in a multicultural team. • Self-starter: Ability to work independently, manage priorities, and take initiative while remaining a team player. • Proficiency in MS Office: Strong skills in Excel and other MS Office applications. • Interest in Laboratory Systems: A passion for learning about electronic systems and IT solutions within the pharmaceutical industry. • Adaptability: Comfortable working in an international environment with diverse teams and stakeholders.

Recipharm is a leading global CDMO dedicated to meeting your evolving needs through operational excellence, scientific know-how, and customer connectivity. We operate development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK and the US and are continuing to grow and expand our offering. Our worldwide reach paired with in-depth, localised market knowledge allows us to anticipate our customers’ needs and strengthen the support we provide to forge a healthier, more expansive and more fruitful future together. With a workforce of 5 200 people, we are focused on supporting pharmaceutical companies with our full-service offering, taking products from early development through to commercial production. Since our inception in 1995, we have supported our customers throughout the entire product lifecycle, providing pharmaceutical expertise and managing complexity, time and time again to ensure their products are delivered with certainty.