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Associate Quality Analyst Jobs in Wisconsin (NOW HIRING)

PCI Pharma Services

Qa Associate I - Ops

Madison, WI · On-site

No The Quality Associate I - Operations is the first of two levels within the QA Associate ... Mayparticipatein root cause analysis using methodologies,such as:fishbone, 5 whys, etc. * Act as QA ...

Aspen Technology, Inc.

WI · On-site

$104.40 - $130.50/hr

... Associate Manager, Software Quality Engineering leading the testing of Aspen Products providing ... Lead the analysis of requirements, creation, and execution of test strategies and test cases ...

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How much do associate quality analyst jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for associate quality analyst in Wisconsin is $32.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $37.36 per hour, depending on experience, location, and employer.

What does an associate quality analyst do?

An Associate Quality Analyst is responsible for assisting in the testing and evaluation of products or software to ensure they meet established quality standards. Their duties typically include executing test cases, documenting defects, and collaborating with developers to resolve issues. They also help maintain quality documentation and participate in continuous improvement initiatives. This entry-level role is essential for supporting the quality assurance team and ensuring the final product is reliable and meets customer expectations.

What are the key skills and qualifications needed to thrive as an associate quality analyst?

To thrive as an Associate Quality Analyst, you need a solid understanding of quality assurance processes, basic knowledge of software testing methodologies, and often a bachelor's degree in a related field. Familiarity with tools like Jira, Selenium, or other test management systems and certifications such as ISTQB can be advantageous. Strong attention to detail, analytical thinking, and effective communication skills help you collaborate with teams and identify issues efficiently. These skills and qualities are crucial to ensuring product quality, reducing defects, and supporting seamless software development cycles.

What are some common challenges faced by an associate quality analyst during software testing cycles?

Associate Quality Analysts often encounter challenges such as managing tight testing deadlines, quickly adapting to evolving project requirements, and effectively communicating defects to development teams. They may also need to balance multiple testing tasks while ensuring thoroughness and accuracy. Collaborating with cross-functional teams and learning new testing tools or methodologies can require adaptability, but overcoming these challenges helps build strong analytical and communication skills for future career growth.

What is the difference between Associate Quality Analyst vs Quality Control Inspector?

AspectAssociate Quality AnalystQuality Control Inspector
CertificationsBasic quality assurance certifications, such as Six Sigma Green BeltOften requires industry-specific certifications or training
Work EnvironmentCollaborative, involves data analysis, testing, and process improvementHands-on inspection, physical testing, and product evaluation
Employer & Industry UsageUsed across manufacturing, software, and service industries for process improvementPrimarily in manufacturing and production for product quality checks

The Associate Quality Analyst focuses on analyzing data, improving processes, and supporting quality assurance initiatives, often working closely with teams to implement standards. In contrast, a Quality Control Inspector primarily conducts physical inspections and tests products to ensure they meet quality specifications. Both roles are essential in maintaining quality but differ in scope and daily tasks.

Is an Associate Quality Analyst a good entry-level job?

An Associate Quality Analyst is typically considered an entry-level position in quality assurance and testing roles. It provides foundational skills in process evaluation, testing methodologies, and tools like Excel or testing software, making it suitable for those starting a career in quality assurance or software testing.

What are the most commonly searched types of Quality Analyst jobs in Wisconsin?

The most popular types of Quality Analyst jobs in Wisconsin are:

Associate Quality Analyst jobs near you
Infographic showing various Associate Quality Analyst job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution, with an average salary of $68,053 per year, or $32.7 per hour.

Associate Scientist II, Quality Control

Arrowhead Pharmaceuticals

Verona, WI • On-site

Full-time

Re-posted 12 days ago

Key responsibilities

  • Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and/or stability samples using established test methods and procedures

  • Performs routine Environmental Monitoring sample collection within a cGMP Manufacturing space

  • Maintains and troubleshoots analytical instrumentation, and reviews test data to ensure compliance with cGMP requirements

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
This position is within the Quality Control structure, under the Quality Organization. An Associate Scientist II, Quality Control will support the analytical testing of pharmaceutical raw materials, in-process samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Associate Scientist II will also support Environmental Monitoring sample collection, support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Associate Scientist II is expected to perform several analytical techniques and can make sound scientific decisions with guidance from management. This position reports to the QC-EM Scientist.
Responsibilities
  • Developing understanding and knowledge of cGMP requirements.
  • With guidance from laboratory leadership, works to meet project timelines and deliverables
  • Performs routine Environmental Monitoring sample collection within a cGMP Manufacturing space.
  • Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and/or stability samples using established test methods and procedures
  • Executes training requirements, applies relevant SOPs and associated procedural guides
  • Ensures that training records are up to date and in compliance
  • Familiar with various analytical instrumentation theory and practice
  • Trains on, and becomes proficient with, a variety of analytical instrumentation (e.g., HPLC, GC, FT-IR, UV/Vis, KF, etc.)
  • Can set up various instrumentation for testing according to written test methods with little to no supervision
  • Plans and executes work related tasks with minimal supervision
  • Performs analyses in a timely manner
  • Works collaboratively with others
  • Shows initiative and interest in learning new techniques and tests
  • Identifies and troubleshoots minor analytical problems with instrumentation, general chemistry and computer applications
  • Quickly communicates analytical or sample issues to senior staff and/or management
  • Maintains a clear, concise and accurate laboratory notebook or worksheet records.
  • Reviews test data acquired by others, as applicable.
  • Aids with the drafting of technical documents such as OOS/atypical investigations, deviations and CAPAs
  • Possesses good written and verbal communication skills
  • Consistently and correctly analyze data/results and interpret outcome of experiments and to propose appropriate follow-up with supervision.
  • Embraces cGMP requirements for all associated work
  • Works cooperatively in a team environment
  • Developing attention to detail
  • Calibration, maintenance, and troubleshooting of analytical equipment with supervision.
  • Remains flexible with changing priorities
  • Additional duties as assigned

Requirements
  • Masters in Chemistry (or related field) with 1+ years' relevant laboratory experience in pharmaceutical/regulated environment or Bachelors in Chemistry (or related field) with 3+ years in a GMP QC or analytical laboratory environment.
  • Experience with cGMP laboratory requirements and operations
  • Familiar with analytical instrumentation, test methodology/validations, data acquisition systems, and cGMP policies and practices.

Preferred
  • Previous Environmental Monitoring and/or cleanroom experience.
  • Previous Microbiology experience.
  • Language Skills: Ability to read, analyze and interpret SOPs, test methods, procedural guides and associated technical documents. Ability to write in a clear and concise manner. Ability to effectively present information and respond to questions from management, peers and colleagues.
  • Mathematical Skills: Must be able to perform complex math functions, compute ratios, rate, and percent. Must be able to draw and interpret graphs and charts.
  • Reasoning Skills: Must be able to solve practical problems. Must be able to interpret a variety of instructions furnished in written, oral, diagram or schedule form.
  • Other Skills and Abilities: Must be able to work with people at various levels of the organization. Must have basic knowledge of computers and PC's. Ability to use windows-based software including MS Office and chromatography data collection software.

Wisconsin pay range
$70,000-$85,000 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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