




Position Summary: Centrient Pharmaceuticals is seeking a Laboratory Technician for R&D, responsible for the analysis and development of analytical methods for APIs and intermediates. Key Highlights: 1. Sample analysis and development of analytical methods for APIs. 2. Experience in development, validation, and transfer of analytical methods. 3. Practical knowledge of GMP regulations and quality standards. Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics and a supplier of next-generation statins and antifungals. We produce and market intermediates, active pharmaceutical ingredients (APIs), and finished pharmaceutical dosage forms. With our commitment to Quality, Reliability, and Sustainability at the core of everything we do, our more than 1\,800 employees continuously work to meet our customers’ needs. We strive for a sustainable future by actively participating in the fight against antimicrobial resistance. We are currently seeking a Laboratory Technician for our R\+D Department. **Requirements** **Main Tasks and Responsibilities:** * Analysis of samples from the development phase and incoming materials (KSMs, reagents, etc.), as well as scale-up batches and demonstration batches. Stability sample analysis. * Development and optimization of analytical methods for quality control of APIs (active pharmaceutical ingredients) and their intermediates. * Interpretation of analytical data to support decision-making. * Validation, verification, and transfer of analytical methods. * Support to the Quality Control (QC) department during method transfer. * Completion of laboratory notebooks with required primary data in accordance with data integrity requirements. * Serve as the point of contact for assigned laboratory teams. * Control and management of stock for reagents, solvents, consumables, and reference standards. **Requirements** * Minimum of 5 years’ prior laboratory experience. * Diploma of Higher Technician in Laboratory Analysis or related qualification. * Proficiency in analytical techniques (HPLC, GC, UV, PSD, MS, etc.). * Experience in development, validation, and transfer of analytical methods. * Practical knowledge of GMP regulations and quality standards. * Experience with Empower and OpenLab. * Proficiency in MS Office tools (Excel, Word, Outlook). * English language proficiency at B1 level. Selection Process Interested candidates must submit their application via the “apply” button, attaching their curriculum vitae. For additional information about the position or about the Recruitment and Selection process, please contact the Human Resources department at HRSpain@centrient.com. Further company information is available at www.centrient.com. Reference checks form part of the company’s Recruitment and Selection process. If necessary, the candidate will be contacted to request the appropriate references.


