Validation Analyst

Description

Position Summary: We are seeking a professional to draft, execute, and report on qualifications, validations, and calibrations at Fresenius Kabi, a global healthcare company. Key Highlights: 1. Drafting and management of qualifications, validations, and calibrations. 2. Generation of essential technical documentation (URS, DQ, IQ, OQ). 3. Management and planning of validation/calibration projects. **Some of your key responsibilities will include:** Drafting, 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. Additionally, Fresenius Kabi is a global leader in blood collection bags and devices, supporting blood banks and healthcare centers worldwide. Our portfolio of generic injectable drugs and intravenous infusion therapy solutions 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, part of \#FutureFresenius, the company continues developing, manufacturing, and commercializing new products and technologies to strengthen its position as a global leader in therapies, improve healthcare delivery, 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 sterile pharmaceutical manufacturing and validations. **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 discounted full membership for company employees. Birthday leave day. Access to the Bimbo Discount Club.