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Weekend Qa Supervisor Jobs in Madison, WI (NOW HIRING)

Perform wise variety of QA related tasks. QC inspection, Maintain training system Qualifications * Hard working and competent * 3-5 years of experience Education: * BS in related field Additional ...

Quality Assurance Specialist

Waunakee, WI · On-site

$62K - $90K/yr

Quality Assurance Specialist The Quality Assurance Specialist ensures that all quality systems, documentation, and processes comply with applicable GMP, FDA, and ISO regulations. This role focuses on ...

Quality Assurance Specialist

Madison, WI · On-site

$62K - $90K/yr

Quality Assurance Specialist The Quality Assurance Specialist ensures that all quality systems, documentation, and processes comply with applicable GMP, FDA, and ISO regulations. This role focuses on ...

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Weekend Qa Supervisor information

See Madison, WI salary details

$24.2K

$86.8K

$159.2K

How much do weekend qa supervisor jobs pay per year?

As of Aug 13, 2026, the average yearly pay for weekend qa supervisor in Madison, WI is $86,817.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,300.00 and $137,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Weekend QA Supervisor, and why are they important?

To thrive as a Weekend QA Supervisor, you need a solid understanding of quality assurance processes, supervisory experience, and a background in relevant industries such as manufacturing or food production. Familiarity with QA software, statistical process control tools, and standards like ISO 9001 or HACCP is typically required. Strong leadership, problem-solving abilities, and effective communication are essential soft skills for managing teams and resolving issues quickly. These skills ensure consistent product quality, regulatory compliance, and efficient weekend operations.

What are the main challenges a Weekend QA Supervisor typically faces, and how can they be addressed?

As a Weekend QA Supervisor, one common challenge is managing a smaller or rotating team during off-peak hours, which can impact workflow and communication. Additionally, you may need to quickly resolve quality issues without immediate access to weekday support staff or management. Success in this role often depends on strong organizational skills, the ability to make independent decisions, and effective communication with both on-site and remote teams. Proactively setting clear expectations and maintaining thorough documentation can help streamline weekend operations and ensure quality standards are consistently met.

What is a Weekend QA Supervisor?

Weekend QA Supervisors are quality assurance professionals who oversee and manage the quality control processes during weekend shifts in manufacturing, production, or service environments. Their responsibilities include supervising QA staff, ensuring compliance with quality standards, addressing quality issues, and maintaining accurate documentation. They play a critical role in maintaining product or service quality when regular weekday management may not be present, ensuring smooth operations and adherence to company policies during weekends.

What is the difference between Weekend Qa Supervisor vs Weekend Quality Assurance Technician?

AspectWeekend Qa SupervisorWeekend Quality Assurance Technician
CertificationsQuality assurance certifications, supervisory trainingQuality assurance certifications, technical training
Work EnvironmentOversees QA team, manages processes, reports to managersPerforms testing, inspects products, documents findings
Employer & Industry UsageManufacturing, food production, pharmaceuticalsManufacturing, food industry, electronics

The Weekend Qa Supervisor typically oversees QA teams and manages quality processes, requiring supervisory skills and certifications. In contrast, the Weekend Quality Assurance Technician focuses on performing tests and inspections directly on products. Both roles are essential in maintaining quality standards but differ in responsibilities and scope.

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago


Job description

JOB SUMMARY

Join our team at Scientific Protein Laboratories (SPL), a world leader in biosourced pharmaceuticals, located just outside of Madison, Wisconsin in Waunakee!  SPL is an innovative biopharmaceutical leader with unique products and services supporting the pharmaceutical industry globally.  For over 40 years, SPL specializes in the development and cGMP compliant manufacturing of Active Pharmaceutical Ingredients (APIs).  SPL has an exciting opportunity to join the team as an On-Site QA Supervisor. This is a 1st shift position.

This position is responsible for supervision of the sites on-site Quality Assurance responsibilities including but not limited to on-site inspection, batch record review and raw material inspection/release. Develops and maintains cGMP-compliant Quality Management Systems. Responsible for management of SPL's quality compliance throughout SPL which includes operational activities such as: release of intermediate product, release assessment of finished product; review of batch records; review of investigations, deviations, change controls and CAPAs; pest control; raw material inspections/release. The supervisor is responsible for personnel activities such as: reviews, workload management and coordination of training.

Responsibilities include:

•  Oversee the functions of the on-site QA staff to include but are not limited to on-site inspection of manufacturing/testing areas, sampling and release of raw materials, pest control, review of manufacturing and packaging batch records and

•  Organize the establishment/maintenance of relevant procedures/documents.

•  Assists all departments in the identification and evaluation of facility events. Assures proper documentation is initiated to capture the event.

•  Determine disposition of packaging materials, in-process materials and products on the basis of approved specifications.

•  Participates in the preparation of Annual Product Review documentation for all SPL Marketed Products.

•  Provide appropriate data and QA support for SPL regulatory functions.

•  Coordinates/reviews deviations, investigations, change controls and CAPAs

•  Participates in audits and addresses audit findings where necessary.

•  Performs intermediate product release and finished product release assessments.

•  Product shipping release.

•  Responsible for continuous improvement of SPL cGMP Quality Systems to support on-site QA in compliance with FDA, ICH, USDA, ISPE and other pertinent pharma industry requirements.

•  Compiles and communicates metrics associated with on-site QA to management as required.

Job Requirements and Qualifications:

  • Education: Associate’s degree required, Bachelor’s degree or above preferred
  • Experience: 5+ years’ required, 10+ years preferred
  • Schedule: 1st shift

WHY JOIN SPL?

Our employees are our success!  We recruit motivated people, recognize their contributions, and support their development to reach their full potential. 

Perks include: competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401k; advancement opportunities; team-oriented environment; community involvement; company events and more!

SPL is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law.