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Quality Control Associate Jobs in Mount Horeb, WI

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Quality Control Associate information

See Mount Horeb, WI salary details

$11

$25

$37

How much do quality control associate jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for quality control associate in Mount Horeb, WI is $25.16, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $30.62 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 Mount Horeb, WI are hiring for Quality Control Associate jobs? Cities near Mount Horeb, WI with the most Quality Control Associate job openings:
Infographic showing various Quality Control Associate job openings in Mount Horeb, WI as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $52,332 per year, or $25.2 per hour.

PCI Pharma Services Pharmaceutical Career Fair - Madison, WI - Friday August 7, 2026

PCI Pharma Services

Madison, WI • On-site

Full-time

Posted 12 days ago


PCI Pharma Services rating

6.7

Company rating: 6.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

437th of 538 rated manufacturers


Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI.


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

PCI is hosting an onsitecareer fairfor multiple positions. At PCI Pharma Services, weprovidea comprehensive range of pharmaceutical services from the earliest stages of developmentthrough tocommercial launch and ongoing supply. We have an uncompromising focus on providing quality and operational excellence and providing the industry with leading customer experience.

  • PCI Pharma Services Pharmaceutical Career Fair

  • Friday, August 7th, 2026

  • 1:00 PM-3:00 PM

  • 5501 Research Park Blvd. Madison, WI

Summary of positions available:

Manufacturing Technician I/II/III:Learn and perform a variety of tasksin accordance withthe manufacturing GMP/ISOrequirementand standards.Performs routine and critical manufacturing operations, including but not limited to work functions in equipment prep, formulation, aseptic compounding, and filling activities for biopharma and medical device products.

Manufacturing TechnicianIV :Leads others in complex manufacturing tasks while ensuring compliance with GMP/ISO and PCI safety standards. Performs and oversees all operations, including equipment prep, dispensing, dissolution, formulation, purification, aseptic compounding, filling, and packaging. Resolvesnonroutineissues using advanced technicalexpertiseand escalates matters as needed. Reviews and updates MPRs and SOPs, monitors team behaviors, trains less experienced staff, andmodelsGuardian values.

Material Handler I/II/III:Assists in the day-to-day activities relating to inventory control functions supporting pharmaceutical fill/finish operations. The main responsibility of this position is toassistwith all aspects oflogisticssuch as receiving, shipping, data entry, inventory control,labelingandmaintainingall associated cGMP documentation as needed.

QA Associate I - Operations: Provides real-time QA support on the floor for GMP Manufacturing of drugproduct. The work scope includes floor oversight of manufacturing includingobservingcritical processes and performing AQL visual inspection,executedGMP documentation review and supporting other QA functions as needed.

QA Specialist I - Aseptic Core Monitoring:Providesrealtimemonitoring of aseptic behaviors during sterile manufacturing, including gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas. Supports PCI's commitment to aseptic integrity, product quality, and patient safety.

QA Specialist I - Operations:Ensures product quality and compliance with internal procedures and external standards.Core responsibilities include Batch Record Review, Lot Disposition, and Quality System oversight.May also evaluate deviations,determineescalation needs, review and approve investigations, and manage associated CAPAs. This roleprovidesthe opportunity to strengthenGxPprograms by delivering QAexpertisefor clinical and commercial manufacturing.

QC Microbiology Technician I:Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and othertasks asassigned by management.

QC MicrobiologistI:Conducts environmental andcleanutilitysampling and testingin accordance withapproved procedures. Performs laboratory analyses and supportsadditionalmicrobiology tasks as assigned by management.

QC Sample Coordinator:Supports daily operations within the QC Sample Management group. The work scope includes executing material control procedures and reviewing specification documents, performing raw material sampling and inspection, coordinating testing activities with internal and external laboratories, and collecting data and material certificates for QA reviews.

Supervisor, Quality:Leads the QA Associates, who provide QA support in the manufacturing of clinical and commercial drug products, to ensure compliance with the principles and guidelines of cGMP.Assistsinmaintainingquality systems, management of investigations, material management, and providing QA support in real time for manufacturing, to ensure control of the manufacturing process.

Visual Inspection Technician I:Performing visual inspection of sterile filled containers (vials)in accordance withall applicable procedures, regulations, and safety directives. The primary job function will be to ensure finished drug product vials manufactured by PCI are free of visible defects which are culled through the visual inspection process to support patient safety and product quality.
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Join us and be part of building the bridge between life changing therapies and patients. Let's talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.


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