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This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

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 manor.

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.

Physical Attributes

Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch or crawl for long periods of time.
Talk, hear, taste and smell.
Occasionally lift and/or move up to 50 pounds unassisted and push and pull heavy materials to complete assignments. May lift more poundage with assistance.
Close vision, distance vision, color vision, peripheral vision, depth vision, and adjust focus.
Use of phones, computers, computer monitors, and all office / laboratory equipment. Type at a computer keyboard and have read CRTS / computer monitors.
Work near moving mechanical parts and wear appropriate protective gear, (hard hats, glasses / goggles, chemical resistant suites, gloves, safety shoes) and other personal protection equipment “PPE” to protect themselves from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles. Work in an environment where highly potent / hazardous materials are handled and manufactured.

Who You Are

Minimum Qualifications:

Bachelor’s in Chemistry, Biology, or other Life Science discipline
5+ years of analytical laboratory environment operating under GLP or cCMP conditions

Master’s in Chemistry, Biology, or other Life Sciences discipline
2+ years of analytical laboratory environment operating under GLP or cCMP conditions

PhD in Chemistry, Biology, or other Life Sciences discipline.
1+ year in an analytical laboratory environment operating under GLP or cGMP conditions.

Preferred Qualifications

Excellent written and verbal communication skills, as well as excellent documentation practices and attention to detail.
Ability to work in a team environment.
Ability to work in an Analytical testing lab with hazardous and toxic chemicals.

Pay Range for this position: $74,500 - $121,800

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

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