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Data Review Scientist
A Data Review Scientist in the Analytical Development group is responsible for leading and executing scientific/technical review of analytical data and reports in support of incoming and existing projects for MilliporeSigma-Madison. This position is responsible for review of data, documentation and reports supporting method development and verification, technology transfer to the Quality Control department, and Process Development and Manufacturing support activities. The data review scientist is also responsible for contributing to discussions and communications with customers to achieve a desired endpoint, initiating and reviewing documentation and methodologies needed to support the project in cGMP manufacturing, and generating and compiling results to solve or diagnose a problem. This will also include interpretation of data generated by state-of-the-art instrumentation as necessary to perform report review. Understanding and interpreting HPLC, GC, LCMS, DSC, TGA, KF, FTIR, NMR and XRPD, among other instrumentation, and wet chemical assays is part of the role. The Data Review Scientist will review and evaluate analytical data and technical reports for identification of products, intermediates and raw materials. You will also complete data review and approval of protocols and standard operating procedures as well as technical reports and specifications. The Data Review Scientist will maintain project timing and interacting with clients to assure project goals are met in an efficient and well documented manner. Working with colleagues in PAD, the Data Review Scientist is part of a team of professionals advancing pharmaceutical candidates to cGMP manufacturing. The Data Review Scientist is considered an expert in analytical chemistry and the requirements for cGMP manufacturing (though the data that will be reviewed will be non-GMP). The Scientist is recognized as a significant individual contributor in the scientific and technical areas within PAD. Perform and lead analytical data and report reviews to ensure accuracy, quality, and compliance with ALCOA+ principles and cGMP standards. Identify and resolve issues in scientific documentation, demonstrating strong scientific literacy and attention to detail. Guide and support team members in documentation practices and data review processes, fostering continuous improvement and training efforts. Interpret and review a wide range of analytical data (e.g., HPLC, GC, LCMS, NMR, FTIR, XRPD) across various tests and instruments. Write, revise, and review SOPs and specifications for raw materials, intermediates, and final products. Collaborate with global teams, internal departments, and external clients to ensure alignment and progress on project goals. Manage multiple projects and timelines independently, ensuring quality, regulatory, manufacturing, and safety considerations are met. Communicate effectively across teams, demonstrating strong organizational and technical writing skills while maintaining a safe and clean work environment.
A Data Review Scientist in the Analytical Development group is responsible for leading and executing scientific/technical review of analytical data and reports in support of incoming and existing projects for MilliporeSigma-Madison. This position is responsible for review of data, documentation and reports supporting method development and verification, technology transfer to the Quality Control department, and Process Development and Manufacturing support activities. The data review scientist is also responsible for contributing to discussions and communications with customers to achieve a desired endpoint, initiating and reviewing documentation and methodologies needed to support the project in cGMP manufacturing, and generating and compiling results to solve or diagnose a problem. This will also include interpretation of data generated by state-of-the-art instrumentation as necessary to perform report review. Understanding and interpreting HPLC, GC, LCMS, DSC, TGA, KF, FTIR, NMR and XRPD, among other instrumentation, and wet chemical assays is part of the role. The Data Review Scientist will review and evaluate analytical data and technical reports for identification of products, intermediates and raw materials. You will also complete data review and approval of protocols and standard operating procedures as well as technical reports and specifications. The Data Review Scientist will maintain project timing and interacting with clients to assure project goals are met in an efficient and well documented manner. Working with colleagues in PAD, the Data Review Scientist is part of a team of professionals advancing pharmaceutical candidates to cGMP manufacturing. The Data Review Scientist is considered an expert in analytical chemistry and the requirements for cGMP manufacturing (though the data that will be reviewed will be non-GMP). The Scientist is recognized as a significant individual contributor in the scientific and technical areas within PAD. Perform and lead analytical data and report reviews to ensure accuracy, quality, and compliance with ALCOA+ principles and cGMP standards. Identify and resolve issues in scientific documentation, demonstrating strong scientific literacy and attention to detail. Guide and support team members in documentation practices and data review processes, fostering continuous improvement and training efforts. Interpret and review a wide range of analytical data (e.g., HPLC, GC, LCMS, NMR, FTIR, XRPD) across various tests and instruments. Write, revise, and review SOPs and specifications for raw materials, intermediates, and final products. Collaborate with global teams, internal departments, and external clients to ensure alignment and progress on project goals. Manage multiple projects and timelines independently, ensuring quality, regulatory, manufacturing, and safety considerations are met. Communicate effectively across teams, demonstrating strong organizational and technical writing skills while maintaining a safe and clean work environment.