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Quality Control Jobs in Oregon, WI (NOW HIRING)

Merck Group

Quality Control Scientist

Verona, WI · On-site

$95K/yr

The Scientist, Quality position is responsible for validating methods and technical transfers as well as providing technical and analytical leadership to the Quality Control department at Millipore ...

Merck Group

Quality Control Scientist

Verona, WI · On-site

$63K - $95K/yr

The Scientist, Quality position is responsible for validating methods and technical transfers as well as providing technical and analytical leadership to the Quality Control department at Millipore ...

Lkqcorp

Quality Control Technician

Janesville, WI · On-site

$20/hr

Inspect parts - matching description and quality to how they were inventoried. * Communicate with sales reps - Using email and/or phone to describe any discrepancies in quality or inventory of the ...

Lkqcorp

Quality Control Technician

Janesville, WI · On-site

$20/hr

Inspect parts - matching description and quality to how they were inventoried. * Communicate with sales reps - Using email and/or phone to describe any discrepancies in quality or inventory of the ...

Actalent

QC Analytical Chemist

Verona, WI

$22 - $25/hr

QC Analytical Chemist 2nd shift: 11:30am - 8:00pm Mon - Thurs & 9:30am - 6:00pm Friday This QC Analytical Chemist role focuses on testing and releasing raw materials used in manufacturing within a ...

New

Integrated Resources INC

Quality Control Tech 3

Madison, WI · On-site

$19 - $24.25/hr

Execute method transfers into QC and write summary reports. Perform method validations and write technical reports. Perform instrument calibration (IQ/OQ/PQ/PM) and routine equipment maintenance ...

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All JobsQuality Control JobsQuality Control Jobs in Oregon, WI

Quality Control information

See Oregon, WI salary details

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How much do quality control jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for quality control in Oregon, WI is $21.08, according to ZipRecruiter salary data. Most workers in this role earn between $16.97 and $23.61 per hour, depending on experience, location, and employer.

What is the job of quality control?

The job of quality control involves inspecting products or services to ensure they meet specified standards and are free of defects. Quality control professionals use testing, measurements, and documentation to identify issues and improve processes, often working with tools like checklists and quality management systems. Strong attention to detail and knowledge of industry standards are essential for this role.

What is the difference between Quality Control vs Quality Assurance?

AspectQuality ControlQuality Assurance
FocusDetecting defects in products or servicesPreventing defects through process improvements
ActivitiesInspections, testing, samplingProcess audits, standards development
CredentialsOften requires technical training or certifications in testingCertifications like ISO, Six Sigma are common
Work EnvironmentLaboratory, production lines, manufacturingProcess development, documentation, audits

While Quality Control focuses on identifying defects after production, Quality Assurance aims to prevent defects through process improvements. Both roles are essential for maintaining product quality, but they differ in approach and activities.

Do you need a degree for quality control?

A degree is not always required for a quality control position, as many employers accept candidates with a high school diploma or equivalent. However, having post-secondary education or certifications in quality management, such as Six Sigma or ISO standards, can improve job prospects and advancement opportunities.

Is quality control a good career choice?

Quality control is a viable career that involves inspecting products and processes to ensure standards are met, often requiring attention to detail and knowledge of industry regulations. It can offer stable employment with opportunities for advancement and may require certifications or training in specific tools or standards. The field is important across many industries, including manufacturing, healthcare, and food production.

What is quality control?

Quality control (QC) is a process by which businesses ensure that their products or services meet specific standards of quality. This typically involves systematic inspection, testing, and corrective actions to detect and address defects or inconsistencies. Quality control helps maintain customer satisfaction, comply with regulations, and reduce waste or costly errors. QC can be applied at various stages of production and is essential in industries such as manufacturing, food production, and pharmaceuticals.

What are some common challenges faced by quality control professionals and how can they be addressed?

Quality Control professionals often encounter challenges such as maintaining consistency across production batches, adapting to new regulatory standards, and managing tight deadlines without compromising quality. Addressing these challenges requires strong attention to detail, effective communication with production and engineering teams, and continuous learning to stay updated on industry best practices. Many companies support their QC staff with regular training sessions, clear documentation protocols, and collaborative problem-solving meetings to ensure quality standards are upheld.

Is quality control a good career path?

Quality control is a viable career that involves inspecting products and processes to ensure standards are met, often requiring attention to detail and knowledge of industry regulations. It can lead to advancement into supervisory or specialized roles and may require certifications such as Six Sigma or ISO standards. The job typically offers stable employment in manufacturing, healthcare, or technology sectors.

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

To thrive as a Quality Control professional, you need keen attention to detail, analytical skills, and a background in science, engineering, or manufacturing, often supported by relevant certifications like Six Sigma or ISO standards. Familiarity with quality management systems (QMS), statistical process control (SPC) software, and inspection equipment is typically required. Strong problem-solving abilities, communication, and teamwork set top performers apart in this role. These skills are crucial to ensure product consistency, prevent defects, and maintain compliance with industry standards.
More about Quality Control jobs
What cities near Oregon, WI are hiring for Quality Control jobs? Cities near Oregon, WI with the most Quality Control job openings:
Quality Control jobs near you
Infographic showing various Quality Control job openings in Oregon, WI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $43,855 per year, or $21.1 per hour.

Quality Control Scientist

Merck Group

Verona, WI • On-site

$95K/yr

Full-time

Medical, Retirement, PTO

Posted 19 days ago

Job description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
The Scientist, Quality position is responsible for validating methods and technical transfers as well as providing technical and analytical leadership to the Quality Control department at Millipore Sigma. Analysis involves the use of HPLC, GC, KF, DSC, TGA, IR, MS, NMR and XRPD among other tests and instruments. The position demonstrates the ability to work on, and solve, problems independently with some guidance. Other responsibilities may include initiation and review of deviations, OOS/OOT's, change controls, and CAPA's. Additionally, participation in process improvement initiatives, and working in a team environment. In this role, you will contribute to the overall success of the company by assisting in many areas beyond specific job duties.
  • Perform method validations, transfers and analytical testing of cGMP materials; ensure data accuracy with proper techniques and documentation.
  • Conduct and contribute to peer review of analytical data (e.g., HPLC, KF, GC) to ensure quality.
  • Train new or less experienced personnel on SOPs, analytical methods, and instrument operation.
  • Maintain a safe, audit-ready, and clean lab environment with rigorous data integrity.
  • Manage lab upkeep: order reagents, ensure clean glassware, dispose of waste properly, and perform general housekeeping.
  • Tackle complex data-analysis problems; apply critical thinking and lead root-cause analysis in OOS/OOT investigations with corrective/preventive actions.
  • Perform instrument PVs and OQs; coordinate with internal and external groups to keep projects on track.
  • Author and revise SOPs and specifications (raw materials to stability); ensure compliance with ICH Q7 and 21 CFR Parts 11/210/211; support right-first-time data integrity.

Physical Attributes:
  • Wear appropriate protective gear (hard hats, lab coats, safety glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protective equipment "PPE"to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors, or airborne particles.
  • Work with highly potent/hazardous materials requiring the use of proper PPE, which could include half/full face respirators, Saranex and/or Tyvek suits with powered respiration.
  • Regularly sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl for extended periods of time.
  • Occasionally lift and/or move up to 30 pounds unassisted, push/pull heavy materials to complete assignments, and lift more poundage with assistance
  • Speak, hear, taste, and smell.
  • Use close vision, distance vision, color vision, peripheral vision, depth vision and adjust focus.

Who You Are:
Minimum Qualifications:
  • Bachelor's Degree in Chemistry, Chemical Engineering, or other Life Science discipline.
  • 5+ years of experience in a GLP or cGMP analytical laboratory environment.

Preferred Qualifications:
  • Experience with method validation.
  • Experience as a project lead.
  • Experience with team and client interactions.
  • Experience with technical writing skills to author operating procedures, protocols and reports.
  • Knowledge and understanding of organic analytical chemistry.

Pay Range for this position: $63,600-$95,500.
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here
RSREMD
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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