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Werfen is looking for a Scientist II in Lliçà d'Amunt, Spain to contribute to assay development in IVD. Responsible for a range of laboratory procedures, selecting experimental methods, and compiling experimental data. Requires a Bachelor's degree in biological sciences and four years of relevant experience, plus fluency in Spanish or Catalan and advanced English. The role may involve sporadic travel. Join a family-owned leader in diagnostics with continuous innovation and growth.br#J-18808-Ljbffr

pGrifols, S.A. is seeking a Bioanalytics Scientist to join the Bioanalytics, CMC Product Development area within the Scientific Innovation Office. /ppThe successful candidate will initiate and coordinate analytical developments, validate methods, and ensure GMP-compliant execution of projects while collaborating cross-functionally. You will design and oversee laboratory studies, analyze data with statistical methods, and present results through reports and presentations. /p #J-18808-Ljbffr

ppWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. /p bWe believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. /b h3Mission /h3 pA Bioanalytics Scientist is sought to join the Bioanalytics, CMC Product Development area within the Scientific Innovation Office at Grifols, a company specialized in the research, development, and manufacturing of purified plasma‑derived therapeutic proteins obtained through the fractionation of human plasma. /p h3Main Mission /h3 pThe successful candidate will be responsible for initiating, planning, coordinating, and executing the technical aspects of assigned projects within the established timelines. They will ensure that all analytical developments, method validations, and related activities are performed in compliance with internal procedures and applicable Good Manufacturing Practice (GMP) regulations. /p h3What Your Responsibilities Will Be /h3 ul liDesign, plan, and oversee laboratory studies and experimental activities to ensure high-quality scientific outcomes. /li liAnalyze and interpret experimental data, including statistical analysis, trend evaluation, and graphical data presentation. /li liPrepare and present scientific results through clear technical reports, presentations, and cross‑functional communications. /li liDevelop, optimize, and validate new laboratory methods in accordance with applicable scientific and regulatory standards. /li liConduct scientific literature reviews and bibliographic research to support project development and innovation. /li liEnsure the stability, characterization, and analytical evaluation of biological products throughout the product lifecycle. /li liAuthor study protocols, technical reports, and scientific documentation, ensuring accuracy, traceability, and compliance with quality requirements. /li /ul h3Who You Are /h3 ul liBachelor's degree in Life Sciences, such as Pharmacy, Biology, Chemistry, Biochemistry, or a related field. /li liA Master's and/or PhD in a relevant discipline is considered an advantage. /li liAt least 2 years of research experience, preferably within the pharmaceutical industry. /li liExperience with in vitro and/or in vivo studies is highly desirable. /li liSolid knowledge of GMP, GLP, ICH guidelines, and other relevant regulatory standards. /li liStrong understanding of statistical analysis and data interpretation. /li liAdvanced English proficiency (C1 level), both written and spoken. /li liProficiency in Microsoft Office, particularly Excel, and experience with GraphPad Prism is a plus. /li liExcellent time management and prioritization skills. /li liStrong communication and presentation abilities. /li liHigh level of analytical thinking, attention to detail, and accuracy. /li liAbility to work effectively in cross‑functional teams. /li liA proactive, committed, and enthusiastic attitude, with a genuine passion for scientific research and continuous improvement. /li /ul h3What We Offer /h3 pIt is a brilliant opportunity for you. Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. /p pWe look forward to receiving your application! We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please let us know. Grifols is an equal opportunity employer. /p bFlexibility for U Program: On site. /b h3Benefits Package /h3 pContract of Employment: Temporary position. /p h3Location /h3 pParets del Vallès, Spain. /p pInformation about Grifols is available at If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! /p /p #J-18808-Ljbffr

pGrifols seeks a Bioanalytics Scientist to join the Bioanalytics, CMC Product Development area within the Scientific Innovation Office. You will initiate, plan, coordinate, and execute analytical activities on assigned projects within established timelines. /ppYou will develop, validate, and ensure GMP-compliant analytical methods, analyze data, prepare technical reports, and collaborate across cross-functional teams. /p #J-18808-Ljbffr

pMango busca un Data Science Global Distribution Analyst para apoyar el desarrollo de soluciones basadas en datos en su equipo de distribución global. El/la candidato/a trabajará en Python/PySpark según directrices técnicas y colaborará con negocio y sistemas para alinear objetivos. /ppSe requiere formación cuantitativa, experiencia inicial en análisis de datos y un alto nivel de inglés. Se valora conocimiento en logística, ventas y herramientas de visualización como Looker/Power BI. /p #J-18808-Ljbffr

ph3Mission /h3 pA Bioanalytics Scientist is sought to join the Bioanalytics, CMC Product Development area within the Scientific Innovation Office at Grifols, a company specialized in the research, development, and manufacturing of purified plasma-derived therapeutic proteins obtained through the fractionation of human plasma. /p h3Main Mission /h3 pThe successful candidate will be responsible for initiating, planning, coordinating, and executing the technical aspects of assigned projects within the established timelines. They will ensure that all analytical developments, method validations, and related activities are performed in compliance with internal procedures and applicable Good Manufacturing Practice (GMP) regulations. /p h3What your responsibilities will be /h3 ul liDesign, plan, and oversee laboratory studies and experimental activities to ensure high-quality scientific outcomes. /li liAnalyze and interpret experimental data, including statistical analysis, trend evaluation, and graphical data presentation. /li liPrepare and present scientific results through clear technical reports, presentations, and cross-functional communications. /li liDevelop, optimize, and validate new laboratory methods in accordance with applicable scientific and regulatory standards. /li liConduct scientific literature reviews and bibliographic research to support project development and innovation. /li liEnsure the stability, characterization, and analytical evaluation of biological products throughout the product lifecycle. /li liAuthor study protocols, technical reports, and scientific documentation, ensuring accuracy, traceability, and compliance with quality requirements. /li /ul h3Who you are /h3 pTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. /p ul liBachelor's degree in Life Sciences, such as Pharmacy, Biology, Chemistry, Biochemistry, or a related field. /li liA Master's and/or PhD in a relevant discipline is considered an advantage. /li liAt least 2 years of research experience, preferably within the pharmaceutical industry. /li liExperience with in vitro and/or in vivo studies is highly desirable. /li liSolid knowledge of GMP, GLP, ICH guidelines, and other relevant regulatory standards. /li liStrong understanding of statistical analysis and data interpretation. /li liAdvanced English proficiency (C1 level), both written and spoken. /li liProficiency in Microsoft Office, particularly Excel, experience with GraphPad Prism is a plus. /li liExcellent time management and prioritization skills. /li liStrong communication and presentation abilities. /li liHigh level of analytical thinking, attention to detail, and accuracy. /li liAbility to work effectively in cross-functional teams. /li liA proactive, committed, and enthusiastic attitude, with a genuine passion for scientific research and continuous improvement. /li /ul h3Benefits package /h3 pFlexibility for U Program: On site. /p pContract of Employment: Temporary position. /p h3Equal Employment Opportunity /h3 pGrifols is an equal opportunity employer. We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help. /p /p #J-18808-Ljbffr

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