Analytical Development Technician
hace 8 horas
Tres Cantos
pulliExperience: Minimum 2 years of relevant experience /li /ul pbWant to know more? /b /p pAt Algenex, we are passionate about advancing biotechnology through the development and manufacturing of recombinant proteins for the formulation of biological medicines. /p pWe are currently looking for an Analytical Development Technician to join our team in Tres Cantos, Madrid. This is an excellent opportunity for a laboratory professional who wants to contribute to analytical development activities in a growing and innovative environment, supporting projects with real impact on the future of biologic products. /p pIf you enjoy combining scientific rigor, technical execution, problem-solving, cross-functional collaboration, and high-quality analytical work in a regulated environment, this role could be your next challenge. /p h3What are we looking for? /h3 pWe are looking for a proactive, detail-oriented, and scientifically driven professional with experience in analytical development, analytical validation, or quality control within the biopharmaceutical or biotechnology industry. /p pIn this role, you will contribute to the development, qualification, and validation of analytical methods, support product development across different stages, and help ensure robust, reliable, and compliant analytical data. /p h3The challenge! /h3 ul liDevelop, qualify, and validate new analytical methods, identifying technical challenges and performing troubleshooting, optimization, and robustness activities. /li liExecute analytical tasks autonomously in support of different stages of Analytical Development and/or Analytical Validation. /li liDesign, follow, review, and contribute to analytical protocols, methods, and departmental procedures. /li liOrganize, analyze, and interpret scientific data, ensuring the technical consistency and reliability of results. /li liDocument activities and results accurately and on time in accordance with cGxP, regulatory requirements, and internal procedures. /li liPlan, execute, analyze, and document stability and validation studies. /li liDraft and review technical documentation such as SOPs, analytical methods, validation protocols, stability plans/protocols, and technical reports. /li liParticipate in the training and onboarding of new team members in analytical techniques, equipment, documentation best practices, safety, and internal workflows. /li liManage and maintain the inventory and status of reagents, standards, and samples, ensuring operational availability. /li liCommunicate effectively with peers, supervisors, and management regarding activity status, risks, and potential deviations. /li liExecute sample testing to support development activities across all product stages, including process development, formulation, characterization, and comparability, when applicable. /li liGenerate and execute validation and stability protocols/plans and associated reports, including sampling point tracking, trending, and result evaluation. /li liPrepare and manage solutions, buffers, standards, and controls. /li liRecord results and observations in a timely and accurate manner, ensuring data integrity and right-first-time documentation. /li liReview and consolidate documentation and results generated by the team when applicable, ensuring complete and consistent records, traceability, and compliance with ALCOA+ principles. /li liProvide support to other company areas depending on business needs and company priorities. /li /ul h3What do you need? /h3 ul liMS, BS, or Higher Vocational Training in Clinical and Biomedical Laboratory or other Life Sciences-related disciplines. /li liMinimum 2 years of relevant experience in the biopharmaceutical or biotechnology industry in analytical development, analytical validation, or quality control. /li liKnowledge and hands-on experience in the development, qualification, and validation of analytical methods for biological products. /li liPractical experience working with biological samples and analytical techniques, including: /li liHPLC: SEC, IEX, Reverse Phase, and Normal Phase /li liELISA: direct, indirect, sandwich, and inhibition /li licIEF /li liCE-SDS /li liWestern Blot /li liSDS-PAGE /li liqPCR /li liUV/Vis /li liOther relevant analytical techniques /li liExperience working in regulated environments and managing technical documentation accordingly. /li liStrong scientific data analysis and interpretation skills. /li liExperience with cGxP, ALCOA+, and technical documentation will be highly valued. /li /ul pFlexible start time from Monday to Friday (full-time) /p ul liBenefits and Savings Club /li liTraining and language learning platform /li liWellness platform with unlimited free psychologist sessions /li liDevelopment plans and internal mobility policy /li /ul h3What will the selection process look like? /h3 ul liInitial contact by phone /li li2 interview stages /li liFinal feedback at the end of the process /li /ul h3Do you think this role is not for you? /h3 pStay connected with Algenex and follow our upcoming opportunities. The right next step in your career might be just around the corner. /p h3EQUAL OPPORTUNITY COMMITMENT /h3 pAt Algenex, we are committed to equal opportunities and to fostering a diverse, inclusive, and respectful workplace. All applications will be considered without discrimination based on gender, gender identity or expression, ethnicity, nationality, religion, sexual orientation, age, disability, or any other characteristic protected by applicable law. /p /p #J-18808-Ljbffr