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Per Diem Analytical Method Development Jobs (NOW HIRING)

WI · On-site

$70 - $90/hr

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 ...

New

Responsibilities Analytical Method Development, Transfer & Validation Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small ...

Lead the development, qualification, validation, and transfer of robust analytical methods, ensuring high-quality data generation and reproducibility.* Collaborate cross-functionally to identify and ...

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Per Diem Analytical Method Development information

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$89K

$191.4K

$287.5K

How much do per diem analytical method development jobs pay per year?

As of Aug 20, 2026, the average yearly pay for per diem analytical method development in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

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 cities are hiring for Per Diem Analytical Method Development jobs?

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

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

The most popular types of Analytical Method Development jobs are:

What states have the most Per Diem Analytical Method Development jobs?

States with the most job openings for Per Diem Analytical Method Development jobs include:

Infographic showing various Per Diem Analytical Method Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.

Senior Scientist I, Analytical Development

Socket.dev

Verona, WI • On-site

$115 - $135/hr

Other

Posted 2 days ago

New


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 a 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 This position is within the Analytical Development (AD) group in the CMC Manufacturing organization. The Senior Scientist I, Analytical Development will provide scientific and technical leadership for analytical activities supporting drug substance and drug product development. This role will lead method development and validation activities and support analytical testing for process development, impurity characterization, GLP toxicology studies, and cGMP clinical trial materials. The Senior Scientist I will work independently and collaboratively across project teams, serve as an analytical lead for assigned programs, and provide technical guidance and mentorship to less experienced scientists. This position reports to Analytical Development management.

Responsibilities
  • Work independently and collaboratively with project teams to deliver accurate, high-quality analytical results in support of new and ongoing development programs.
  • Provide technical leadership, guidance, and mentorship to junior scientists.
  • Serve as Analytical Project Coordinator or Lead for assigned programs, taking ownership of analytical activities, including planning, prioritizing, and coordinating testing to meet project timelines and deliverables.
  • Independently design, develop, optimize, and validate analytical methods supporting all stages of 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 and interpret complex analytical data, troubleshoot technical challenges, and recommend appropriate follow-up activities.
  • Prepare and review technical documentation, including analytical test methods, development and validation protocols and reports, SOPs, and presentations.
  • Communicate project status, analytical results, risks, and recommendations to project teams and management.
  • Ensure analytical activities are conducted in accordance with applicable SOPs, cGMP requirements, regulatory guidelines, and industry standards.
  • Contribute to continuous improvement of analytical methods, laboratory practices, and departmental processes.
  • Perform other duties as assigned.
Requirements
  • Ph.D. in Chemistry or a related scientific discipline with 2+ years of relevant experience; M.S. with 10+ years of relevant experience; or B.S. with 12+ years of relevant experience.
  • Demonstrated experience in analytical method development, optimization, qualification, and validation supporting pharmaceutical drug substance and drug product development.
  • Experience developing analytical methods and specifications for raw materials, intermediates, drug substances, and drug products.
  • Demonstrated experience with analytical instrumentation and pharmaceutical development processes.
  • Experience independently analyzing complex data, troubleshooting analytical challenges, and recommending appropriate solutions.
  • Experience leading analytical activities or serving as an analytical representative on cross-functional project teams.
  • Proficiency with analytical techniques and instrumentation such as HPLC, GC, FTIR, UV/Vis, LC/MS, Karl Fischer (KF), and related technologies.
  • Strong knowledge of analytical instrumentation principles, test methodologies, and method validation.
  • Strong understanding of CMC regulatory requirements and applicable cGMP, ICH, and FDA/CDER guidelines.
  • Knowledge of the principles of synthetic organic chemistry.
  • Strong scientific judgment, problem-solving, and data interpretation skills.
  • Excellent organizational skills with the ability to manage multiple priorities and project timelines.
  • Strong written and verbal communication skills.
  • Strong attention to detail and commitment to data quality and integrity.
  • Ability to work effectively both independently and within cross-functional teams.
Preferred
  • Experience providing technical guidance, training, or mentorship to junior scientists.
  • Experience serving as an analytical project lead or coordinator for pharmaceutical development programs.
  • Experience supporting analytical activities across multiple stages of drug development.
  • Demonstrated ability to influence scientific direction and effectively communicate technical recommendations across functions.

Wisconsin pay range $115,000 — $135,000 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. California Applicant Privacy Policy

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