Job Purpose As a Senior Scientist I, you will lead laboratory studies, develop and validate cutting-edge bioanalytical and immunological assays, and ensure compliance with GxP and global regulatory standards. You’ll oversee study execution, guide teams, contribute to high-quality reporting, and collaborate with clients—playing a key role in advancing impactful scientific projects. Main Areas of Responsibility Lead study specific laboratory staff and ensure compliance with GxP and latest guidelines. Write and review SOPs and support method documentation. Develop, validate, and apply bioanalytical and immunological assays for pre-clinical, clinical studies, and drug batch characterization as Responsible Scientist (RS), Study Director (SD) or Principal Investigator (PI). Study specific consultation, capacity management, reagent planning, inventory, troubleshooting, and training. Conduct and manage sample analysis, validaton and method development studies. Draft and review project documents (e.g., lab manuals, validation plans, sample analysis reports), ensuring high-quality reporting and client communication. Lead studies, manage pre- and post-contract phases (change order management, reagent plans, protocols, quotes), and support revenue generation. Maintain ERP timesheets and unit logging, provide training, and contribute to achieving monthly revenue targets. Stay updated on bioanalysis trends, continuous GxP-related training, implement EMA/FDA guidelines, assess systems for improvements, and share knowledge regularly. Ensure compliance with regulatory guidelines by maintaining SOPs, policies, and study documentation, and providing staff training and support. Qualifications & Experience Required: Master’s degree in a natural science or 4-5 years’ relevant experience. Strong knowledge of analytical techniques and hands-on experience with LC/MS and GxP principles (GLP, GCP, GMP, GCLP). Proficient with advanced instruments (e.g., Mass Spectrometry). Proficient in following protocols, and using standard equipment (centrifuges, biosafety cabinets, incubators). Good command of written and spoken English, with strong collaboration and negotiation skills. Desirable: Experience in GxP-accredited labs. Willingness to travel as needed. PLEASE ENSURE THAT YOUR CV/RESUME IS SUBMITTED IN ENGLISH.