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Data Review Scientist

5+ years
Not Disclosed
10 Sept. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Data Review Scientist

📍 Location: Madison, Wisconsin, United States
🆔 Job ID: 290818
📌 Job Type: Full-time

About Us

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
We innovate across Healthcare, Life Science, and Electronics—driven by curiosity and passion to enrich people’s lives. Join us in imagining the unimaginable.

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

Your Role

As a Data Review Scientist in the Analytical Development group, you will lead and execute scientific and technical reviews of analytical data and reports for new and ongoing projects. You will play a critical role in ensuring data integrity, supporting technology transfers, and contributing to process development and manufacturing activities.

Key Responsibilities:

Perform and lead reviews of analytical data and reports to ensure accuracy, quality, and compliance with ALCOA+ and cGMP standards.

Review data and documentation supporting method development, verification, and technology transfer.

Interpret and assess results from advanced instrumentation (HPLC, GC, LCMS, DSC, TGA, KF, FTIR, NMR, XRPD, and wet chemistry assays).

Review and approve protocols, SOPs, technical reports, and specifications.

Collaborate with internal teams (PAD, QC, Process Development, Manufacturing) and external clients to achieve project goals.

Manage multiple projects independently, ensuring quality, regulatory, and safety requirements are met.

Guide team members in documentation and data review practices, supporting training and continuous improvement initiatives.

Communicate effectively across teams, demonstrating strong technical writing and organizational skills.

Physical Requirements

Sit, stand, walk, stoop, kneel, twist, or crouch for extended periods.

Lift/push/pull up to 50 lbs unassisted; heavier weights with assistance.

Full range of vision (close, distance, color, peripheral, depth).

Frequent use of computers, phones, and laboratory equipment.

Work near moving mechanical parts and hazardous chemicals, wearing required PPE (glasses, gloves, safety shoes, respirators, Tyvek suits, etc.).

Handle highly potent and hazardous materials in laboratory/manufacturing environments.

Who You Are
Minimum Qualifications:

Bachelor’s degree in Chemistry, Biology, or Life Sciences + 5 years analytical lab experience (GLP/cGMP)
OR

Master’s degree in Chemistry, Biology, or Life Sciences + 2 years analytical lab experience (GLP/cGMP)
OR

PhD in Chemistry, Biology, or Life Sciences + 1 year analytical lab experience (GLP/cGMP)

Preferred Qualifications:

Excellent documentation, written, and verbal communication skills.

Ability to interpret and review complex analytical data.

Team-oriented, detail-focused, and strong organizational skills.

Experience working safely with hazardous and toxic chemicals.

Compensation & Benefits

💰 Pay Range: $74,500 – $121,800 annually

Final compensation depends on location, experience, education, and skills.

Eligible for sales or performance-based bonuses.

Benefits include:

Health insurance

Paid Time Off (PTO)

Retirement contributions

Additional perquisites

What We Offer

At MilliporeSigma, we value diverse perspectives and experiences. We foster inclusion, innovation, and career growth—empowering every individual to work their magic and champion human progress.

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