Validation Analyst

Description

Job Summary: Responsible for writing, executing, and reporting qualifications and validations; generating technical documentation; and managing projects in a pharmaceutical environment. Key Highlights: 1. Writing and execution of qualifications, validations, and calibrations. 2. Generation of technical documentation (URS, DQ, IQ, OQ). 3. Management and planning of validation/calibration projects. **Key responsibilities include:** Writing, execution, and reporting of qualifications, validations, and calibrations. Generation of technical documentation (URS, DQ, IQ, OQ). Management and planning of validation/calibration projects. Development and updating of the validation schedule. As a global healthcare company, Fresenius Kabi is Committed to Life. Our products, technologies, and services are used in the therapy and care of critically ill and chronically ill patients. With more than 43\.000 employees worldwide and presence in over 100 countries, Fresenius Kabi’s broad product portfolio focuses on providing access to high-quality, life-saving medicines and technologies. In Clinical Nutrition, we offer a comprehensive portfolio of enteral and parenteral nutrition products that significantly improve patients’ nutritional status. In MedTech, the company provides essential infusion pumps, cell and gene therapy devices, medical supplies, and more. Furthermore, Fresenius Kabi is a world leader in blood collection bags and devices, supporting blood banks and healthcare centers globally. Our portfolio of generic injectable drugs and intravenous solutions for infusion therapy helps save millions of lives each year in areas such as emergency medicine, surgery, oncology, and intensive care. Fresenius Kabi adopts an integrated approach to healthcare, combining expertise, knowledge, innovation, and commitment—impacting the lives of nearly 450 million patients annually. With its Vision 2026 strategy, as part of \#FutureFresenius, the company continues developing, manufacturing, and marketing new products and technologies to strengthen its position as a global leader in therapies, improve patient care, and generate sustainable value for its stakeholders—contributing to the future of health. Requirements **Education:** University degree or advanced student (mandatory) in Pharmacy, Biochemistry, Engineering, or related fields. **Experience:** Preferred experience in the sterile pharmaceutical industry and validation activities. **Working Hours:** Full-time. Monday to Friday, 08:00–17:00. Availability to work on weekends. **English:** Intermediate level. Personal transportation preferred. Benefits On-site cafeteria. **SportClub:** special discount for company employees on full membership. Birthday leave day. Access to the Bimbo Discount Club.