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Quality Control Associate Jobs in Mineral Point, WI

Sabrosura Foods

General Labor 1st Shift

Monticello, WI · On-site

The DMC Processing Associate LV3 plays a critical role in ensuring the accurate and efficient ... Familiarity with database management systems and data quality control tools. * Prior experience ...

Sabrosura Foods

General Labor 3rd Shift

Monticello, WI · On-site

$21.49/hr

The DMC Processing Associate LV3 plays a critical role in ensuring the accurate and efficient ... Familiarity with database management systems and data quality control tools. * Prior experience ...

The Dental Office

Associate Dentist

Lancaster, WI · On-site

$250K - $300K/yr

... quality family dental care. Our dentist and staff provide general services, including teeth ... The successful candidate will ensure adherence to HIPAA regulations and infection control protocols ...

Hibbett Retail, Inc.

Sales Associate

Platteville, WI · On-site

$10 - $12.50/hr

... quality customer service. The Sales Associate is knowledgeable in each product area or department ... control procedures and informing management and/or appropriate officials of potential fraud risk.

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Mineral Point, WI

Quality Control Associate information

See Mineral Point, WI salary details

$11

$25

$38

How much do quality control associate jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for quality control associate in Mineral Point, WI is $25.57, according to ZipRecruiter salary data. Most workers in this role earn between $18.61 and $31.15 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 cities near Mineral Point, WI are hiring for Quality Control Associate jobs?

Cities near Mineral Point, WI with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Mineral Point, WI 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 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $53,178 per year, or $25.6 per hour.

Senior Quality Control Associate Scientist-Madison, Wisconsin

Mount Horeb, WI

Merck Group
See more jobs at Merck Groupexternal

$24 - $39/hr

Full-time

Medical, Retirement, PTO

Posted 3 days ago

New

Job description

Work Location: Madison, Wisconsin
Shift:
Department: LS-SC-UYWQFC QC Release, MSN
Hiring Manager: Evan Schmitz
This information is for internals only. Please do not share outside of the organization.
Your Role:
The Madison 1st shift Scientist, Quality Associate Senior position is responsible for cGMP analytical laboratory analysis in the Quality Control department of MilliporeSigma. Primary responsibilities include oversight of reference standard program and coordination of material requests with internal and external partners. Analysis/review may consist of all/some of the following: incoming raw material analysis, in-process testing, final product analysis, method validation/qualification, cleaning, and environmental monitoring to support Quality Control activities at the Madison and Verona sites. Analysis includes techniques specific to, but not limited to: HPLC, GC, KF, DSC, TGA, IR, MS, NMR and XRPD among other tests and instruments. Other responsibilities may include initiation and review of deviations, OOS/OOT's, change controls, and CAPA's. Additionally, participation in process improvement initiatives, working in a team environment, maintaining a clean and safe work area, and supporting the department in maintaining the laboratory in an audit ready state are other duties. The Scientist, Quality Associate Senior position will require a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.
Physical Attributes:
  • Work in an analytical testing lab with hazardous and toxic chemicals.

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

Preferred Qualifications:
  • 4+ years of experience in a GMP manufacturing or testing laboratory
  • Understanding of 21 CFR Part 11, 210 and 211, and ICH Q7
  • Experience with chemical analyses including HPLC, GC, KF, DSC, TGA, IR, MS, NMR, and/or XRPD
  • Excellent written and verbal communication skills and good documentation practices and attention to detail
  • Knowledge and understanding of analytical chemistry techniques

Pay Range for this position: $24-$39 per hour.
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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