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Quality Control Associate Jobs in Wisconsin (NOW HIRING)

Faithtechnologies

Electrical QA/QC Engineer

Menasha, WI · On-site

... QC activities. This work is completed under the general oversight of an upper level QA Engineer ... Associate of Applied Science Degree Experience: 5 years of hands-on field commissioning experience ...

Simos

Quality Control Line Tech

Port Washington, WI · On-site

$17 - $17.50/hr

Description Staff management is hiring a Quality Control Line Technician for one of the world ... Proven ability to maintain confidentiality and discretion with information Associate Requirements

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How much do quality control associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for quality control associate in Wisconsin is $25.70, according to ZipRecruiter salary data. Most workers in this role earn between $18.70 and $31.30 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

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

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

What cities in Wisconsin are hiring for Quality Control Associate jobs?

Cities in Wisconsin with the most Quality Control Associate job openings:

What are popular job titles related to Quality Control Associate jobs in WI?

For Quality Control Associate jobs in WI, the most frequently searched job titles are:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $53,458 per year, or $25.7 per hour.

Associate Scientist II, Quality Control

Arrowhead Pharmaceuticals

Verona, WI • On-site

Full-time

Re-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
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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