Job Description

With practical experience in LC, LC/MS laboratories and interest in cell-based applications, you have established a high level of technical proficiency. Taking this knowledge to the next level is now With practical experience in LC, LC/MS laboratories and interest in cell-based applications, you have established a high level of technical proficiency. Taking this knowledge to the next level is now possible. Join a dynamic, market-leading group involved in application focus and strategic marketing. You will be an asset to our dynamic, growing team as an Application Development Engineer/Scientist. Working with recognized scientists engaged in the definition and application of cutting-edge biopharmaceutical techniques and workflows, you will interact with top clients, Product Managers, and Design Engineers. Your technical expertise in liquid chromatography/Cell based analytical skills will be critical to help define and market current and future LC, LC/MS and Cell analysis instrumentation. You will develop applications and proof of performance on new and existing instrumentation and provide critical feedback and insight to product design and current marketing efforts. You will be a key player in growing Agilent Technologies portfolio and market leadership in Biopharma industry. Job Responsibilities: Roles and responsibilities include but not limited to: Lead the development of integrated solutions: a key contributor of scientific and technical expertise in the respective industry/market. Develop and manage validation projects with internal/external collaborators to ensure successful partnerships and completion of accurate technical collateral information. Reduce broad concepts workflow analysis strategies into structured requests and new projects. Solve complex, high impact scientific problems. Work with R&D colleagues to design workflow solutions to meet customer needs. Act as business unit liaison for new product introductions. Provide input to segment marketing on new workflow concepts. Traveling to scientific conferences and exhibitions may be required. Job Qualifications Require a M.S., Ph.D., or equivalent degree in analytical chemistry related to Pharma/Biopharma, Life Sciences. At least 3 to 5 years of relevant experience in process validation, familiar with GLP requirements, analytical methods development ideally in LC, LC/MS, Cell analysis and validation required. Experience in drug discovery, development and Quality Control. Ideal candidate would have worked in a core lab providing support for drug discovery (chemistry), metabolite ID and have familiarity with a range of analytical techniques including LC, LC/MS, GC/MS, molecular spectroscopy and Cell biology. Able to collect and maintain data required for compliance verification. Maintain appropriate laboratory notebooks, write reports, and periodically update to the respective crew. Highly proficient English language skills, oral and written. Record of scientific publications/ presentations and proficiency in the use of Microsoft Office tool. Ability to perform appropriate scientific review of documents. Ability to work under pressure, adjust to changing priorities and meet urgent deadlines. Critical thinking and analytical skills, as well as strong written and verbal skills. Able to articulate complex scientific problems into simple terms and understanding. Demonstrates project management capabilities, good teamwork skills and creative thinking.