Quality Assurance Intern Jobs in Madison, WI
Quality Assurance Intern jobs in Madison are concentrated in the University Research Park, downtown, and the East Washington Avenue corridor, driven by demand from biotech, medical devices, software, and food manufacturing employers. Companies actively hiring include Foremost Farms, Promega Corporation, and Arrowhead Pharmaceuticals. Find a role that fits below and apply directly.
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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
Provides quality oversight for GLP/GCLP-compliant bioanalytical and biomarker activities. The QA Specialist II is responsible for conducting audits, collaborating with stakeholders, and ensuring that studies are compliant with regulatory standards.
Responsibilities
- Independently plan, conduct, and report study-specific audits, including method validation and sample analysis phases.
- Review and approve study protocols, validation reports, and analytical plans for QA compliance.
- Audit raw data (chromatography, LIMS) for integrity and regulatory alignment.
- Support regulatory readiness efforts, including preparing responses to audit findings.
- Manage QA activities across assigned clinical and nonclinical studies.
- Lead non-conformance investigations and draft comprehensive CAPAs.
- Proactively identify areas for quality improvement and update audit tools or SOPs accordingly.
- Serve as QA liaison for assigned projects and ensure proper documentation in systems like LIMS or Vault.
- May mentor QA Specialist I personnel and contribute to their onboarding.
Requirements
- Bachelor's degree in a scientific field.
- 3+ years of GLP/GCLP QA experience in pharma or CRO settings.
- Knowledge of OECD GLP, FDA/EMA regulations, ICH M10, and 21 CFR Part 11.
- Working experience auditing HPLC, LC-MS/MS, and ELISA.
- Excellent communication skills and experience drafting audit reports.
- Excellent interpersonal, verbal, and written communication skills.
- Ability to consistently communicate with external parties in a professional manner.
- Ability to follow company procedures, work instructions, and policies.
- Excellent attention to detail and organizational skills.
- Ability to work independently with minimal supervision as well as manage priorities within a fast-paced environment.
Preferred
- Master's degree
- ASQ Certified Quality Auditor (CQA) or equivalent certification.
- Experience supporting biologics, gene therapies, or biomarkers in oncology or rare disease programs.
- Familiarity with electronic systems including Veeva Vault QMS, LIMS, and eTMF.
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
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
Provides quality oversight for GLP/GCLP-compliant bioanalytical and biomarker activities. The QA Specialist II is responsible for conducting audits, collaborating with stakeholders, and ensuring that studies are compliant with regulatory standards.
Responsibilities
- Independently plan, conduct, and report study-specific audits, including method validation and sample analysis phases.
- Review and approve study protocols, validation reports, and analytical plans for QA compliance.
- Audit raw data (chromatography, LIMS) for integrity and regulatory alignment.
- Support regulatory readiness efforts, including preparing responses to audit findings.
- Manage QA activities across assigned clinical and nonclinical studies.
- Lead non-conformance investigations and draft comprehensive CAPAs.
- Proactively identify areas for quality improvement and update audit tools or SOPs accordingly.
- Serve as QA liaison for assigned projects and ensure proper documentation in systems like LIMS or Vault.
- May mentor QA Specialist I personnel and contribute to their onboarding.
Requirements
- Bachelor's degree in a scientific field.
- 3+ years of GLP/GCLP QA experience in pharma or CRO settings.
- Knowledge of OECD GLP, FDA/EMA regulations, ICH M10, and 21 CFR Part 11.
- Working experience auditing HPLC, LC-MS/MS, and ELISA.
- Excellent communication skills and experience drafting audit reports.
- Excellent interpersonal, verbal, and written communication skills.
- Ability to consistently communicate with external parties in a professional manner.
- Ability to follow company procedures, work instructions, and policies.
- Excellent attention to detail and organizational skills.
- Ability to work independently with minimal supervision as well as manage priorities within a fast-paced environment.
Preferred
- Master's degree
- ASQ Certified Quality Auditor (CQA) or equivalent certification.
- Experience supporting biologics, gene therapies, or biomarkers in oncology or rare disease programs.
- Familiarity with electronic systems including Veeva Vault QMS, LIMS, and eTMF.
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
See All 96 Quality Assurance Intern Jobs in Madison
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Find Quality Assurance Intern JobsQuality Assurance Intern Job Market in Madison
Who's Hiring
- Foremost Farms13
- Promega Corporation13
- Arrowhead Pharmaceuticals13
- Catalent Pharma Solutions13
- VIVA6
Quality Assurance Intern Jobs in Madison: Frequently Asked Questions
How do I get a quality assurance intern job in Madison?
Focus your search on Madison's strongest hiring sectors: biotech and life sciences firms near University Research Park, software companies downtown, medical device manufacturers on the east side, and food and beverage producers in the surrounding industrial corridors. Candidates with coursework in statistics, process improvement, or regulatory compliance stand out. Applying directly through company career pages and targeting companies with established internship pipelines gives you an edge in Madison's tight, relationship-driven market.
Which companies hire quality assurance interns in Madison?
Employers hiring quality assurance interns in Madison right now include Foremost Farms, Promega Corporation, and Arrowhead Pharmaceuticals, based on current listings on Migrate Mate as of November 2026. Madison's mix of university-affiliated research spinoffs, established medical device firms, and mid-size software companies means internship openings appear across a range of employer sizes and sectors throughout the year.
Are there remote quality assurance intern jobs in Madison?
Yes, though availability depends heavily on the role. Analytical and documentation-focused QA work, such as test case writing, defect tracking, and compliance review, adapts well to remote settings, while hands-on lab, manufacturing, or hardware testing roles almost always require on-site presence. About 37% of quality assurance intern openings tied to Madison are remote or hybrid as of November 2026. Software and data-oriented QA roles at Madison tech companies tend to offer the most scheduling flexibility.
How can I get a quality assurance intern job in Madison with little or no experience?
The most realistic entry path in Madison is leveraging the UW-Madison connection. Many local biotech, software, and manufacturing employers run structured internship programs specifically designed for students with limited experience, prioritizing coursework over a prior work history. Applying to QA technician or junior test associate roles at smaller East Washington corridor manufacturers or University Research Park startups is a strong local approach. Familiarity with spreadsheets, basic testing tools, or ISO documentation gives applicants a concrete advantage.
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See All 96 Quality Assurance Intern Jobs in Madison
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