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Senior Protein Engineer Jobs in Wisconsin (NOW HIRING)

Showing results 21-32

Senior Protein Engineer information

What is the difference between Senior Protein Engineer vs Protein Scientist?

AspectSenior Protein EngineerProtein Scientist
Required CredentialsBachelor's or Master's in Biochemistry, Molecular Biology, or related fields; experience in protein engineeringBachelor's or Master's; often a Ph.D. for advanced research roles; expertise in protein analysis
Work EnvironmentBiotech or pharmaceutical R&D labs, manufacturing facilitiesAcademic labs, research institutions, biotech companies
Employer & Industry UsageUsed in biotech, pharma, and industrial enzyme companiesCommon in academic research, biotech R&D, and pharmaceutical development

While both roles focus on proteins, Senior Protein Engineers typically work on designing and optimizing proteins for industrial applications, whereas Protein Scientists often conduct fundamental research to understand protein functions. The roles overlap in skills and industry but differ in focus and seniority.

What is a senior protein engineer?

Senior Protein Engineers are experienced scientists who design, modify, and optimize proteins for specific industrial, medical, or research applications. They use advanced techniques in molecular biology, biochemistry, and computational modeling to improve protein stability, activity, or specificity. These professionals often lead research projects, mentor junior staff, and collaborate with interdisciplinary teams to bring innovative protein-based solutions to market.

What skills and qualifications are needed to be a senior protein engineer?

To thrive as a Senior Protein Engineer, you need expertise in protein biochemistry, molecular biology, and structural biology, typically supported by a Ph.D. or equivalent experience in a related field. Proficiency in tools such as protein modeling software (e.g., Rosetta, PyMOL), high-throughput screening platforms, and familiarity with analytical instruments like mass spectrometers is essential. Strong problem-solving, collaboration, and project management skills help drive innovation and successful cross-functional teamwork. These skills and qualities are crucial for efficiently designing, optimizing, and characterizing proteins to advance scientific discoveries and product development.

How much does a senior protein engineer make?

A senior protein engineer typically earns between $90,000 and $150,000 annually, depending on experience, location, and industry. They often work in biotech or pharmaceutical companies, utilizing skills in molecular biology, protein design, and laboratory techniques.

How does a senior protein engineer collaborate with cross-functional teams during the development of new protein therapeutics?

Senior Protein Engineers often work closely with multidisciplinary teams, including molecular biologists, biochemists, computational scientists, and regulatory specialists, to bring new protein therapeutics from concept to reality. They contribute their expertise in protein design and engineering, lead experimental planning, and interpret complex data to guide project direction. Regular meetings and collaborative problem-solving sessions are common, ensuring that project goals align across departments. This collaborative environment fosters innovation, but also requires strong communication and project management skills.

What are the most commonly searched types of Protein Engineer jobs in Wisconsin?

The most popular types of Protein Engineer jobs in Wisconsin are:

What are popular job titles related to Senior Protein Engineer jobs in Wisconsin?

For Senior Protein Engineer jobs in Wisconsin, the most frequently searched job titles are:

What cities in Wisconsin are hiring for Senior Protein Engineer jobs?

Cities in Wisconsin with the most Senior Protein Engineer job openings:

Infographic showing various Senior Protein Engineer job openings in Wisconsin as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution.

Senior Data Reviewer, Quality Control

Arrowhead Pharmaceuticals

Verona, WI • On-site

$100K - $110K/yr

Full-time

Posted 10 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
The Senior Data Reviewer serves as a technical subject matter expert responsible for oversight of complex laboratory data review activities supporting operations. This role provides advanced expertise in data integrity, audit trail review, GMP compliance, and risk-based decision-making to ensure the accuracy, reliability, and inspection readiness of internal and external laboratory data. The Senior Data Reviewer leads complex investigations, drives continuous improvement initiatives, mentors junior staff, and partners cross-functionally to strengthen compliant and efficient review practices.
Responsibilities
  • Perform advanced technical review of internal data and external CDMO datasets for compliance with specifications, GDP, and data integrity requirements
  • Serve as SME for data integrity, audit trail review, and documentation standards
  • Lead complex data review investigations, compliance assessments, and root cause evaluations related to deviations, discrepancies, and data integrity concerns
  • Ensure all data and documentation are maintained in a state of inspection readiness
  • Review and approve routine release and stability data, method validation data and report, cleaning data, IPC data, and critical manufacturing support records.
  • Provide oversight of external laboratory/CDMO data quality and compliance
  • Serve as a primary representative during regulatory inspections, client audits, and compliance assessments
  • Assess compliance and data integrity risks, develop mitigation strategies, and drive corrective and preventive actions to reduce operational and regulatory risk
  • Lead continuous improvement initiatives focused on strengthening data review effectiveness, inspection readiness, workflow efficiency, and digital enablement strategies
  • Mentor and train Data Reviewers I and II; provide technical guidance and troubleshooting support
  • Partner with leadership to ensure milestones, timelines, and compliance objectives are achieved
  • Influence departmental procedures, review standards, and compliance strategies through technical expertise and risk-based decision-making
  • Embrace statistical tools for trend analysis, system suitability trending, deviation investigations, and overall laboratory performance.
  • Other duties as assigned

Requirements
  • Bachelor's degree in chemistry or (any STEM degree) and 8+ years of experience or master's degree and 5+ years of experience in a cGMP laboratory (pharmaceutical CMO/CRO).
  • Strong experience with analytical methods + data review + audit trail review
  • Deep knowledge of GMP, data integrity, and regulatory expectations
  • Working knowledge and experience with chemistry analytical methods such as HPLC, GC, LC-MS, NMR, FTIR, Appearance, pH, KF, UV spectrometry and microbiology testing.

Preferred
  • Working knowledge of USP, ISO, FDA and ICH guidelines
  • Familiarity with laboratory information systems.
  • Strong verbal and written communication skills and ability to work with diverse professionals in a matrix environment.
  • Solid organizational skills with ability to adapt to changing priorities and deadlines.

Wisconsin pay range
$100,000-$110,000 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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