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

Integrated Resources INC

Quality Control Tech 3

Madison, WI · On-site

$19 - $24.25/hr

We deliver strategic workforce solutions that help you manage your talent and business more ... Execute method transfers into QC and write summary reports. Perform method validations and write ...

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Quality Control Manager information

See Madison, WI salary details

$30.7K

$81.9K

$130.5K

How much do quality control manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for quality control manager in Madison, WI is $81,944.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $100,800.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

What is the difference between Quality Control Manager vs Quality Assurance Supervisor?

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

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

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.
More about Quality Control Manager 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 Manager jobs in Madison, WI? For Quality Control Manager jobs in Madison, WI, the most frequently searched job titles are:
What job categories do people searching Quality Control Manager jobs in Madison, WI look for? The top searched job categories for Quality Control Manager jobs in Madison, WI are:
What cities near Madison, WI are hiring for Quality Control Manager jobs? Cities near Madison, WI with the most Quality Control Manager job openings:
Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Madison, WI as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 20% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $81,944 per year, or $39.4 per hour.

Scientist I, Quality Control

Arrowhead Pharmaceuticals

Verona, WI • On-site

Full-time

Re-posted 21 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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