Laboratory Technician - Analytical Development
Eurofins Scientific is an international Life Sciences company that offers a wide range of Analytical Services oriented towards the life sciences. Our clients are from very diverse sectors. The Eurofins group is a world leader in the analysis of products ranging from the food we eat, to the water we drink, or the medicines prescribed to us. Eurofins works with the largest companies in the world to ensure that the products they supply are safe, that their ingredients are authentic, and that the labeling is accurate. Eurofins is the world leader in testing food, environmental, pharmaceutical, and cosmetic products, as well as agroscience. It is also one of the leading independent global market leaders in certain laboratory testing and services for genomics, pharmacology discovery, forensics, CDMO, advanced materials science, and clinical study support.
In just over 30 years, Eurofins has grown from a laboratory in Nantes, France, to having more than 63,000 employees distributed across a network of more than 1,000 independent companies in more than 60 countries, operating more than 950 laboratories. Eurofins offers a portfolio of more than 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability, and purity of biological substances and products, as well as innovative clinical diagnostic testing services, being one of the main emerging global players in specialized clinical diagnostic testing.
In 2025, Eurofins generated total revenues of 7.296 billion euros and has been one of the best-performing companies in Europe over the last 20 years.
EUROFINS, a leading company in providing specialized laboratory services to the pharmaceutical sector, is selecting an Analytical Development Technician for its facilities in Esplugues de Llobregat.
Reporting to the Supervisor of the Analytical Development Department, your basic functions will consist of: Analysis using HPLC, GC, IR, UV, and other techniques related to analytical method development. Method validation. Data analysis and processing. Preparation of Protocols. Preparation of reports. Management of OOS, OOT incidents, and deviations. Management of information generated in the laboratory through LIMS.
Degree or master's in Chemistry, Biology, or similar. 2-3 years of experience in a similar position in the pharmaceutical or related industry. Experience in analytical testing using HPLC /GC and/or HPLC-MS / GC-MS will be valued. Experience in a GMP/GLP environment will be valued. Experience in method validations and in the preparation of protocols and reports will be positively valued. Experience in LIMS, SAP… will be positively valued. Accustomed to working in a team and goal-oriented. High level of English.
Immediate start. Indefinite contract. Schedule: Monday to Friday from 13:30 to 21:30 and one Sunday every 4 weeks. During the training period, the schedule will be from 09:00 to 17:30.