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Associate Scientist Analytical Development Jobs in Wisconsin

Realta Fusion Inc.

Associate Computational Scientist

Madison, WI · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Associate Scientist will support ongoing research and development activities related to plasma ... Support analysis and interpretation of simulation & experimental data using scientific programming ...

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Associate Scientist Analytical Development information

What are the key skills and qualifications needed to thrive as an associate scientist analytical development, and why are they important?

To thrive as an Associate Scientist Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a bachelor’s or master’s degree. Familiarity with analytical techniques like HPLC, GC, mass spectrometry, and relevant laboratory information management systems (LIMS) is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are important soft skills for this role. These competencies ensure accurate data generation, regulatory compliance, and successful collaboration in the development of pharmaceutical products.

What are some common challenges an associate scientist analytical development might face when working on new drug formulations?

Associate Scientists in Analytical Development frequently encounter challenges such as developing robust analytical methods for complex or novel drug formulations and ensuring these methods meet regulatory standards. Balancing tight project timelines with the need to thoroughly validate methods can also be demanding. Additionally, they often need to troubleshoot unexpected results and collaborate closely with cross-functional teams—including formulation scientists and quality assurance—to resolve technical issues and deliver reliable data. These challenges require strong problem-solving skills and adaptability.

What does an associate scientist analytical development do?

An Associate Scientist in Analytical Development is responsible for designing, conducting, and analyzing experiments to develop and validate analytical methods used in the testing of pharmaceutical products. They work closely with cross-functional teams to ensure the quality and consistency of drug formulations by using various laboratory techniques such as chromatography, spectroscopy, and wet chemistry. Their role is critical in supporting drug development, regulatory submissions, and ensuring products meet industry standards.

What is the difference between Associate Scientist Analytical Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Analytical DevelopmentAssociate Scientist Quality Control
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experienceBachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing
Work EnvironmentResearch and development labs, method development, process optimizationQuality control labs, testing, sample analysis, compliance with regulations
Employer & Industry UsagePharmaceutical, biotech companies, focus on method developmentPharmaceutical, biotech companies, focus on product testing and quality assurance

Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

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Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in Wisconsin as of August 2026, with employment types broken down into 57% Full Time, 38% Contract, and 5% Nights. Highlights an 100% In-person job distribution.

Senior Scientist II, Discovery Analytical Chemistry

Arrowhead Pharmaceuticals

Madison, WI • On-site

$92K - $126K/yr

Full-time

Posted 28 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

Arrowhead is seeking a highly motivated and experienced Senior Scientist on Analytical Chemistry to lead analytical method development, characterization, and testing activities supporting pharmaceutical development programs. This role will be responsible for developing and qualifying analytical methods, overseeing analytical activities performed at contract development and manufacturing organizations (CDMOs), and authoring analytical sections of regulatory submissions. The successful candidate will serve as a technical expert in Antibody oligo conjugate (AOC) drug characterization and will collaborate closely with Process Development, Manufacturing, Quality, Regulatory Affairs, and external partners.

Responsibilities

  • Design, develop, optimize, qualify, and transfer analytical methods to support development and manufacturing activities.
  • Lead analytical characterization studies for drug substances, intermediates, and related materials.
  • Develop and execute analytical strategies to assess product identity, purity, potency, impurities, and stability.
  • Interpret analytical data, investigate trends, and provide scientific recommendations to project teams.
  • Support method lifecycle management, troubleshooting, and continuous improvement activities.
  • Provide scientific and technical oversight of analytical development, testing, method qualification, and transfer activities conducted at CDMOs.
  • Review protocols, reports, deviations, investigations, and technical documents generated by external partners.
  • Monitor project timelines, deliverables, and analytical performance to ensure project objectives are achieved.
  • Serve as the primary analytical subject matter expert during interactions with CDMOs and contract testing laboratories.
  • Collaborate with Process Development, Manufacturing, Quality Control, Quality Assurance, Regulatory Affairs, and CMC teams to support program milestones.
  • Contribute to analytical control strategy development and product specification setting.
  • Present analytical findings and recommendations to internal teams and management.
  • Author and review analytical sections of regulatory submissions, including INDs, IMPDs, CTAs, BLAs, and other global regulatory filings.
  • Support responses to regulatory agency questions and inspections.
  • Ensure analytical activities comply with applicable GMP, ICH, FDA, EMA, and other regulatory requirements.
  • Participate in quality investigations, change controls, risk assessments, and CAPA activities as needed.

Requirements

  • PhD in analytical chemistry or close related fields with 5+ years pharmaceutical relevant industry experience; or M.S. with 8+ years of relevant industry experience; or B.S. with 10+ years of relevant industry experience.
  • Extensive knowledge of Oligo, mAb, ADC or AOC-related analytical techniques and applications.
  • Demonstrated expertise with chromatographic methods, including HPLC, UHPLC, and related analytical platforms.
  • Experience with GMP-regulated analytical development and testing environments.
  • Strong understanding of method transfer, validation, and lifecycle management principles.
  • Experience authoring analytical CMC documentation for regulatory submissions.
  • Strong scientific problem-solving and troubleshooting skills.
  • Excellent technical writing and communication abilities.
  • Ability to manage multiple projects in a fast-paced environment.
  • Strong organizational skills and attention to detail.
  • Effective collaborator with demonstrated ability to influence cross-functional teams and external partners.

Preferred

  • Hands-on Experience with Size Exclusion Chromatography coupled with Multi-Angle Light Scattering (SEC-MALS) is preferred but not necessary.
  • Experience supporting biologics, oligonucleotides, ADC, AOC or other complex modalities.
  • Prior experience managing external laboratories and CDMOs.
  • Familiarity with ICH guidelines and global regulatory expectations.
Wisconsin pay range
$130,000—$150,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

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