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Per Diem Analytical Method Development Jobs in Wisconsin

WI · On-site

You support the development, improvement and/or transfer of analytical methods and assist in the writing of reports. You support the organization during internal and external audits. For this ...

Lead comparability studies to support method, process, or product changes. Partner closely with R&D ... Lead analytical gap assessments and risk evaluations to identify, prioritize, and proactively ...

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Per Diem Analytical Method Development information

What is the difference between Per Diem Analytical Method Development vs Per Diem Quality Control Analyst?

AspectPer Diem Analytical Method DevelopmentPer Diem Quality Control Analyst
Primary RoleDevelops and validates analytical methods for testing pharmaceuticalsPerforms routine testing and analysis of pharmaceutical products
Work EnvironmentLaboratory focused on method creation and validationLaboratory conducting routine quality testing
Required CredentialsBachelor's degree in Chemistry or related field; experience in method developmentBachelor's degree in Chemistry or related field; experience in quality testing

Per Diem Analytical Method Development specialists focus on creating and validating new analytical methods, while Per Diem Quality Control Analysts perform routine testing to ensure product quality. Both roles require similar educational backgrounds but differ in their primary responsibilities and work focus.

What are the most commonly searched types of Analytical Method Development jobs in Wisconsin?

The most popular types of Analytical Method Development jobs in Wisconsin are:

What cities in Wisconsin are hiring for Per Diem Analytical Method Development jobs?

Cities in Wisconsin with the most Per Diem Analytical Method Development job openings:

Infographic showing various Per Diem Analytical Method Development job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Senior Scientist I, Analytical Development

Madison, WI • On-site

Scorpion Therapeutics
51 - 200 employees

$115K - $135K/yr

Other

Posted 10 days ago


Job description

Responsibilities:
  • Work independently and collaboratively with project teams to deliver accurate, high-quality analytical results.
  • Provide technical leadership, guidance, and mentorship to junior scientists.
  • Serve as Analytical Project Coordinator or Lead; take ownership of analytical activities (planning, prioritizing, coordinating testing to meet timelines).
  • Independently design, develop, optimize, and validate analytical methods for drug substance/API and drug product development.
  • Develop specifications and test methods for raw materials, in-process materials, intermediates, drug substances, and drug products.
  • Lead analytical activities supporting process development, impurity characterization, GLP toxicology studies, and cGMP clinical trial materials.
  • Analyze/interprete complex data, troubleshoot technical challenges, and recommend follow-up activities.
  • Prepare/review technical documentation (test methods, development/validation protocols and reports, SOPs, presentations).
  • Communicate status, results, risks, and recommendations to project teams and management.
  • Ensure work is performed per SOPs, cGMP requirements, regulatory guidelines, and industry standards.
  • Contribute to continuous improvement; perform other duties as assigned.
Requirements:
  • Ph.D. (2+ yrs), M.S. (10+ yrs), or B.S. (12+ yrs) in Chemistry or related field.
  • Analytical method development, optimization, qualification, and validation for pharmaceutical drug substance and drug product.
  • Experience developing analytical methods/specifications for raw materials, intermediates, drug substances, and drug products.
  • Proficiency with instrumentation/techniques: HPLC, GC, FTIR, UV/Vis, LC/MS, Karl Fischer (KF).
  • Strong knowledge of instrumentation principles, test methodologies, and method validation.
  • Strong understanding of CMC regulatory requirements and applicable cGMP, ICH, and FDA/CDER guidelines.
  • Knowledge of synthetic organic chemistry principles; strong judgment, problem-solving, data interpretation.
  • Excellent organizational skills, communication, attention to detail, data quality/integrity; ability to work independently and cross-functionally.
  • Candidates must have current, valid authorization to work in the country where this role is located.
Preferred:
  • Experience mentoring/training junior scientists.
  • Experience serving as analytical project lead/coordinator.
  • Experience supporting analytical activities across multiple stages of drug development.
  • Demonstrated ability to influence scientific direction and communicate technical recommendations.
Benefits/Pay:
  • Wisconsin pay range: $115,000 USD - $135,000 USD.
  • Competitive salaries and an excellent benefit package.
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