ph3Analytical Development Scientist – Biological Methods /h3 pApplications to be sent to: /p h3Global Responsibility /h3 pResponsible for the execution, documentation, and technical integrity of analytical activities related to the development of bioanalytical methods within the organization. /p pThis includes ensuring that all analytical work—method development, validation, transfer, and routine support—is performed in compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), data integrity standards (ALCOA+), and internal Quality Management Systems (QMS). /p h3Specific Responsibilities /h3 ul liReview the documentation associated as well as documentation of reports, in accordance with GMP standards. Approve the analytical documentation /li liPreparation of presentations and reports results and communicating with the relevant people involved /li liAnalyze samples of finished product and raw intermediate materials if necessary /li liProduce documentation required by the Quality System /li liReview the work performed by the analysts and correct deviations from the established methodology. /li liWrite protocols to describe how to perform the activities required /li liWrite a transfer and verification protocols and reports and coordinate the analysis /li liOrganize and might perform Training of new analysts. /li liManage priorities of analytical projects assigned.



/li liWrite procedures and analytical methods for its use in the Biological Laboratory /li liContribute and design practices for the good functioning of the laboratory /li liWrite technical SOPs when required and participate in their continuous review. /li /ul h3Experience and Personal Skills /h3 ul libEducation: /b A bachelor´s degree in sciences. A PhD would be a plus. /li libLanguages: /b Fluent English and Fluent Spanish. /li libExperience: /b 3-5 years (Senior Scientist) of experience as an analytical scientist in RD, pharma industry. Expert in LC-MS and QTOF (essential requirement), development and validation of biological methods (peptides, proteins, antibodies), processing of samples from plasma, serum, and other blood-derived fluids, experience in the pharmaceutical industry and GMP environments. /li libPersonal skills: /b Resolution, good organizational skills, persistency and autonomy. Able to work independently, prioritize and meet project timelines, be strongly self-motivated and able to motivate a team. Ability to work in a fast-paced environment and manage multiple competing demands. /li /ul h3Additional Information /h3 pInnovation, customer orientation, communication, team work, adaptability/flexibility, productivity, self-development, sense of urgency, initiative. /p pExperience in GMP environment, knowledge of ICH, FDA and EMEA regulatory guidances is a plus. /p pKnowledge of: Peptide mapping -peptidomics-, disulfide bridge analysis, glycosylation characterization, absolute quantification of proteins. /p h3Seniority level /h3 pMid-Senior level /p h3Employment type /h3 pFull-time /p h3Industries /h3 pPharmaceutical Manufacturing /p /p #J-18808-Ljbffr

📌 AnalyticalDevelopment Scientist – Biological Methods (Valencia)
🏢 Bionanopharma
📍 Valencia