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Qa Engineer Jobs in Middleton, WI (NOW HIRING)

Quality Assurance Reporting To: Quality Assurance Operations Supervisor Responsible For (Staff): No The Quality Associate I - Operations is the first of two levels within the QA Associate jobfamily ...

... quality systems, engineering design fundamentals, regulatory authority expectations and industry standards, as well as review and approve relevant documents. You will perform quality oversight of all ...

New

FUJIFILM Cellular Dynamics, Inc. is seeking an expert in validation engineering who will apply knowledge of qualification and validation principles to manufacturing processes, quality systems ...

New

... quality systems, engineering design fundamentals, regulatory authority expectations and industry standards, as well as review and approve relevant documents. You will perform quality oversight of all ...

Continuously improve QA/QC processes to enhance project efficiency and reliability. * Travel to ... Strong understanding of engineering drawings, specifications, and industry standards (ASME, ASTM ...

The Position The position within the Quality Assurance department will support ongoing programs for ... Serve as a resource to mentor Quality Assurance members in Quality Engineering functions (e.g ...

Showing results 41-60

Qa Engineer information

See Middleton, WI salary details

$36.6K

$95.5K

$139K

How much do qa engineer jobs pay per year?

As of Aug 25, 2026, the average yearly pay for qa engineer in Middleton, WI is $95,506.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,300.00 and $111,900.00 per year, depending on experience, location, and employer.

What is a QA engineer?

QA Engineers, or Quality Assurance Engineers, are professionals responsible for ensuring that software products meet established quality standards before they are released to customers. They design and execute tests, identify bugs or issues, and work closely with development teams to resolve problems. QA Engineers play a crucial role in the software development lifecycle by preventing defects, improving product reliability, and ensuring a smooth user experience. Their work may involve manual testing, automated testing, and creating test documentation.

What does a QA engineer do?

As a QA engineer, you monitor the development process and design troubleshooting tests to ensure software or manufacturing materials have no significant issues. If your tests identify problems with the software, you then send the review and feedback to the product design team so they can make plans to debug the software and return it to you for further testing. Your duties include designing various tests, scenarios, and scripts to assess whether or not a piece of software is ready for release. You also track and document your findings using a bug tracking system and participate in design review meetings to provide reports on your results.

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

To thrive as a QA Engineer, you need a solid understanding of software testing principles, programming or scripting knowledge, and familiarity with quality assurance methodologies, often supported by a degree in computer science or a related field. Experience with test automation tools (such as Selenium or JUnit), bug tracking systems, and sometimes certifications like ISTQB are typically required. Attention to detail, analytical thinking, and strong communication skills help QA Engineers identify issues and collaborate effectively with development teams. These skills ensure the delivery of reliable, high-quality software products that meet user requirements and business goals.

How does a QA engineer typically collaborate with developers and other team members during the software development lifecycle?

QA Engineers work closely with developers, product managers, and sometimes UX/UI designers throughout the software development lifecycle. They participate in sprint planning meetings, provide input on testability during requirements discussions, and collaborate with developers to understand new features and identify potential issues early. Regular communication helps ensure that quality standards are met and bugs are addressed promptly, resulting in a more efficient release process and higher-quality products. This collaborative environment also provides QA Engineers with opportunities to expand their technical knowledge and grow within the team.

What is the difference between Qa Engineer vs Software Tester?

AspectQa EngineerSoftware Tester
CertificationsISTQB, CSTE, CSQAISTQB, CSQA (optional)
Work EnvironmentInvolved in automation, process improvement, and quality strategyPrimarily manual testing and test case execution
ResponsibilitiesDesigning test plans, automation, defect analysis, quality assuranceExecuting test cases, reporting bugs, verifying fixes
Industry UsageUsed across software development companies, especially in Agile and DevOpsCommon in traditional and Agile environments

The main difference between a Qa Engineer and a Software Tester lies in their scope and responsibilities. Qa Engineers typically focus on automation, quality processes, and strategic testing, while Software Testers mainly perform manual testing and bug reporting. Both roles are essential for ensuring software quality, but Qa Engineers often have a broader role in quality assurance and process improvement.

Are QA engineers paid well?

QA engineers typically earn competitive salaries that vary based on experience, location, and industry. Entry-level positions may start lower, but with skills in automation tools and testing frameworks, salaries tend to increase significantly for experienced professionals. Overall, QA engineering is considered a well-paying role within the tech industry.

Is QA engineer a stressful job?

A QA engineer's job can be stressful during tight deadlines, bug fixes, or complex testing scenarios, but it often involves structured processes and collaboration. The level of stress varies depending on the company, project scope, and workload, and skills in time management and communication can help manage pressure.

What are the most commonly searched types of Qa Engineer jobs in Middleton, WI?

The most popular types of Qa Engineer jobs in Middleton, WI are:

What job categories do people searching Qa Engineer jobs in Middleton, WI look for?

The top searched job categories for Qa Engineer jobs in Middleton, WI are:

What cities near Middleton, WI are hiring for Qa Engineer jobs?

Cities near Middleton, WI with the most Qa Engineer job openings:

Infographic showing various Qa Engineer job openings in Middleton, WI as of August 2026, with employment types broken down into 87% Full Time, 8% Part Time, and 5% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $95,506 per year, or $45.9 per hour.

Qa Associate I - Ops

Madison, WI • On-site


PCI Pharma Services

6.7

Company rating: 6.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

442nd of 544 rated manufacturers

Paid breaks

Respectful managers

Uninterrupted breaks


Full-time

Posted 14 days ago


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.

SECOND SHIFT

Position Title: QA Associate I - Operations

Location: Madison, Wisconsin

Department: Quality Assurance

Reporting To: Quality Assurance Operations Supervisor

Responsible For (Staff): No

The Quality Associate I - Operations is the first of two levels within the QA Associate jobfamily Theassociate I provides real-time QA support on the floor for GMP Manufacturing of drug product. 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.Real timecontinuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phaseappropriate GMPmanufacture of drug products

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Perform QA On-the-Floor activities supporting client projects, including room release, auditing critical processes, reviewing documentation in real time, and resolving issues that occur during manufacturing
  • Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and Good Documentation Practices
  • Review executed Manufacturing Batch Records and supporting documentation for completeness,accuracyand compliance
  • Support the evaluation and lot disposition of intermediates, finish bulk drugsubstanceand drug product
  • Act as first responder for on the floor quality issuesin a timely manner, documentation of all events/investigations andrequiredimmediate corrective actions
  • Mayparticipatein root cause analysis using methodologies,such as:fishbone, 5 whys, etc.
  • Act as QA reviewer for deviations and CAPA issuance; with limited approval authority asdesignatedby QA Management
  • Perform Acceptable Quality Limit (AQL) visual inspection of drug product
  • Participate in SOP revision as it pertains to process improvements
  • Participate in site quality and process improvement initiatives. Represent QA on project teams and represent QA perspective as necessary
  • Guide personnel indirectly and directly involved in GMP operationspertaining tocGMP compliance, internal procedures, regulatoryrequirementsand industry best practices

QUALIFICATIONS:

Required:

  • Bachelor's Degree in a relevant scientific discipline preferred with a minimum of 0-2 years of pharmaceutical or biotech industry experience with 1+ years of experience in a QA Operations role supportinglate stageclinical and/or commercial production preferred
  • Exposure to RCA, technical writing, and working with quality related investigations
  • Exposure to lean operation excellence highly desirable
  • Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as ICH
  • Knowledge and ability to apply basic scientific principles to solve operational, as well as routine quality tasks
  • Knowledge and exposure to using Risk Management Tools (FMEA, HACCP, PHA, etc.) and familiarity with ICH Q9 preferred
  • ASQ certification preferred

#LI-RS1

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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