Demonstrated experience coaching and/or training others for complex and highly technical work. Demonstrates a high level of initiative and leadership capabilities. Highly collaborative as well as independent. Excellent oral and written communication skills that have been demonstrated through presentations/seminars, oversight of projects, implementation of new services, etc. Experience in Biologics, HPLC and/or CESDS. 
Intermediate skills inLIMS, BRIQS, MS Office suite. Broad working knowledge of product characterization and experience with laboratory practices, techniques, equipment, materials and mathematical calculations. Bachelor's degree in a scientific field (i.e., Biology, Chemistry, BioEngineering, etc.) with 5+ years laboratory experience. Master's degree in a scientific field (i.e., Biology, Chemistry, BioEngineering, etc.) with 2+ years laboratory experience -OR. in a scientific field (i.e., Biology, Chemistry, BioEngineering, etc.) with 1+ years laboratory experience -OR. Complies with company health and safety regulations and procedures. Acts as key driver/ champion on project teams. Contribute ideas and suggestions to improve standard laboratory techniques, protocols, processes and equipment. Performs training of laboratory personnel as needed/ assigned. Writes technical reports for internal use and collaborates on papers for external use. Creates/ revises SOPs, laboratory records and other related documentation as assigned. Maintains a working knowledge of lab procedures and assays. Liaise with Quality Assurance and appropriate cross-functional departmental areas to close the events and corrective actions identified during GxP laboratory testing. Communicates deviations/ events, progress and interim results to Study Management. Utilizes problem solving/ trouble shooting skills. Utilizes applicable computer programs during testing and routine tasks (i.e., Word, Excel, Oracle, LIMS, BRIQS, etc.). Operates and maintains lab equipment as required by SOPs and testing procedures. Makes detailed observations, documents results and performs data analysis. Maintains complete and comprehensive records for study integrity. 
For GLP studies, acts as Study Director.Independently applies basic scientific principles in the design of experiments and the development of assays.Applies laboratory techniques and skills to complete experiments designed to address a variety of specific problems.Act as subject matter expert (SME) for specific defined area(s) of business.Performs testing in accordance with SOPs and regulations (cGMP and GLP).
Requirements also include maintaining a thorough understanding of company testing services, technical principles, regulations and applications as they apply to your position. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards.
MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.Īs a Scientist 1 your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. A career with MilliporeSigma is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics.
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