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Quality Control Assistant Jobs in Madison, WI (NOW HIRING)

PCI Pharma Services

QC Sample Coordinator II

Madison, WI · On-site

$20 - $27.50/hr

Quality Control / Incoming materials and samples coordinator Reporting To: Manager, Quality Control ... Submit all applicable sample submission paperwork to the appropriate testing labs * Assist with ...

PCI Pharma Services

QC Sample Coordinator II

Madison, WI

$20 - $27.50/hr

Quality Control / Incoming materials and samples coordinator Reporting To: Manager, Quality Control ... Submit all applicable sample submission paperwork to the appropriate testing labs * Assist with ...

MasTec Industrial

Quality Inspector, (CWI)

Madison, WI · On-site

$35.64 - $55.30/hr

Methodical and detail-oriented to assist the project team in assuring that Project QC documentation is complete and procedures are followed to ensure issues are closed and project risk is mitigated.

Mastermold LLC

Quality Technician

Johnson Creek, WI · On-site

$20 - $28/hr

... * Assist with control plans, PFMEAs, SPC, audits, and continuous improvement. * Partner with ... Manufacturing quality control, quality assurance, or inspection experience. * Experience using ...

Mastermold LLC

Quality Technician

Johnson Creek, WI · On-site

$20 - $28/hr

... * Assist with control plans, PFMEAs, SPC, audits, and continuous improvement. * Partner with ... Manufacturing quality control, quality assurance, or inspection experience. * Experience using ...

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Quality Control Assistant information

See Madison, WI salary details

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How much do quality control assistant jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for quality control assistant in Madison, WI is $23.01, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $23.27 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality control assistant, and why are they important?

To thrive as a Quality Control Assistant, you need strong attention to detail, basic understanding of quality assurance principles, and at least a high school diploma or equivalent. Familiarity with industry-specific inspection tools, measurement instruments, and software such as Microsoft Excel or specialized quality management systems is often required. Excellent organizational skills, effective communication, and the ability to work both independently and collaboratively set top performers apart. These skills are crucial for ensuring products consistently meet quality standards and for supporting efficient production processes.

What do quality control assistants do?

Quality control assistants inspect products, materials, or processes to ensure they meet quality standards and specifications. They often use testing tools, follow detailed procedures, and document findings to help maintain product consistency and safety in manufacturing or production environments.

What is a quality control assistant?

Quality Control Assistants are professionals who help ensure that products or services meet established quality standards. They assist in inspecting, testing, and evaluating materials or products during various stages of production. Their responsibilities often include recording data, reporting defects, and supporting the implementation of quality assurance procedures. By maintaining high quality standards, they help companies reduce errors, improve customer satisfaction, and comply with industry regulations.

What are some common challenges quality control assistants face when ensuring product consistency, and how can they overcome them?

Quality Control Assistants often encounter challenges such as identifying subtle defects in products, maintaining accurate records under time pressure, and effectively communicating quality issues to production teams. Overcoming these challenges requires keen attention to detail, strong organizational skills, and the ability to collaborate with colleagues from different departments. Regular training on inspection standards and open communication with supervisors can help QC Assistants stay updated and maintain high-quality results.

What is the difference between Quality Control Assistant vs Quality Inspector?

AspectQuality Control AssistantQuality Inspector
CertificationsBasic quality assurance training, sometimes certifications like Six Sigma or ISO awarenessMore advanced certifications often preferred, such as Certified Quality Inspector (CQI)
Work EnvironmentAssist in quality checks, support documentation, and process monitoring in manufacturing or production settingsConducts detailed inspections, tests products, and ensures compliance with standards on the production line
Employer & Industry UsageUsed across manufacturing, food production, and assembly industries as entry-level or support roleCommonly employed in manufacturing, aerospace, automotive, and electronics industries for quality assurance

While both roles focus on quality assurance, the Quality Control Assistant typically supports inspection processes and documentation, whereas the Quality Inspector performs detailed product inspections and testing. The roles often overlap, but the inspector usually has more specialized training and responsibilities.

More about Quality Control Assistant jobs
What are the most commonly searched types of Quality Control jobs in Madison, WI? The most popular types of Quality Control jobs in Madison, WI are:
What are popular job titles related to Quality Control Assistant jobs in Madison, WI? For Quality Control Assistant jobs in Madison, WI, the most frequently searched job titles are:
What job categories do people searching Quality Control Assistant jobs in Madison, WI look for? The top searched job categories for Quality Control Assistant jobs in Madison, WI are:
What cities near Madison, WI are hiring for Quality Control Assistant jobs? Cities near Madison, WI with the most Quality Control Assistant job openings:
Quality Control Assistant jobs near you
Infographic showing various Quality Control Assistant job openings in Madison, WI as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 23% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $47,869 per year, or $23 per hour.

Scientist I, Quality Control

Arrowhead Pharmaceuticals

Verona, WI

Full-time

Re-posted 26 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. A Scientist I, Quality Control will support the analytical testing of Environmental monitoring samples, pharmaceutical raw materials, in­ process manufacturing samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Senior Scientist I will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Senior Scientist I is expected to be proficient in several analytical techniques and will be capable of making independent scientific decisions. The position also requires the ability to lead and mentor co-workers. This position reports to QC Laboratory Management.

Responsibilities

  • Fully knowledgeable of cGMP requirements and ICH guidelines
  • Works independently to meet project timelines and deliverables with minimal supervision to no supervision
  • Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols
  • Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures
  • Proficient with various analytical instrumentation theory and practice
  • Executes training requirements for assigned SOPs and participates in department specific training modules.
  • Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples
  • Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation as
  • Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization
  • Performs analyses in a timely and efficient manner to support ongoing prioritized studies
  • Works closely with other department personnel for efficient project execution and timely/accurate deliverables while building a relationship with respect and communication
  • Trains and mentors co-workers (analysts)
  • Shows initiative and interest in mastering new techniques and tests
  • Ability to track/trend data and interpret degrative changes to the product on stability
  • Uses stability tracking software as a repository generated results (data entry, review and approval).
  • Owns and leads scientific technical discussions and brainstorming sessions
  • Identifies and troubleshoots analytical method issues with instrumentation, general chemistry, test methodology and sample product
  • Communicates laboratory testing issues or challenges to laboratory management
  • Maintains a clear, concise, and accurate notebook
  • Performs technical data review on data acquired by other QC analysts as applicable
  • Drafts technical documents such as COAs, investigations, deviations, and CAPAs
  • Possesses excellent written and verbal communication skills
  • Embraces cGMP and ICH requirements for all associated work
  • Works cooperatively in a team environment
  • Demonstrates a high attention to detail
  • Calibration, maintenance, and troubleshooting of analytical equipment with little to no guidance from management
  • Routinely makes sound, scientific decisions independently and serves as a back-up to Laboratory Management
  • Demonstrates enduring flexibility and understanding with changing priorities.

Requirements

  • M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience
  • B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience
  • Fully knowledgeable of cGMP and ICH laboratory requirements and operations
  • Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices
Wisconsin pay range
$90,000—$108,000 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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