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Quality Assurance Associate Jobs in Iowa (NOW HIRING)

The Greenbrier Companies

QA Manager

Red Oak, IA · On-site

Summary The Quality Assurance Manager position is responsible for providing support to the GBX facility to ensure that products and workmanship meet Greenbrier, customer, and applicable regulatory ...

National Beef

Quality Assurance Supervisor

Tama, IA · On-site

Quality Assurance Supervisor responsibilities include but are not limited to: * Implementing the training of new hires, cross-training activities, and development of entirely new functions * Working ...

National Beef

Quality Assurance Supervisor

Tama, IA · On-site

Responsibilities Quality Assurance Supervisor responsibilities include but are not limited to: * Implementing the training of new hires, cross-training activities, and development of entirely new ...

Harris

Quality Assurance Analyst

Nevada, IA · On-site +1

$55K - $65K/yr

Primary Functions Reporting to the Mobile Team Lead, the Quality Assurance Analyst's key responsibilities will include: * Create, maintain, and execute test plans, test cases, and test scripts for ...

Cambrex

Quality Assurance Engineer

Charles City, IA · On-site

Job Overview The Quality Assurance Engineer is responsible for being the liaison between our generic clients and Charles City with regards to request for documentation to support their regulatory ...

National Beef

Quality Assurance Supervisor

Tama, IA · On-site

Responsibilities Quality Assurance Supervisor responsibilities include but are not limited to: * Implementing the training of new hires, cross-training activities, and development of entirely new ...

Cambrex Corp.

Quality Assurance Engineer

Charles City, IA · On-site

$65 - $95/hr

Job Overview The Quality Assurance Engineer is responsible for being the liaison between our generic clients and Charles City with regards to request for documentation to support their regulatory ...

IMT Insurance

QA Analyst

West Des Moines, IA · Hybrid

$53K - $67K/yr

QA ANALYST IMT Software Services, a division of IMT Insurance, is now looking to fill the position of QA Analyst. IMT Software Services is the industry-leading software provider for farm mutual ...

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Quality Assurance Associate information

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How much do quality assurance associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for quality assurance associate in Iowa is $27.51, according to ZipRecruiter salary data. Most workers in this role earn between $17.60 and $32.31 per hour, depending on experience, location, and employer.

What does a quality assurance associate do?

A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.

What skills and qualifications are needed to be a quality assurance associate?

To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.

What are common challenges faced by quality assurance associates in ensuring consistent product quality?

Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.

What is the difference between Quality Assurance Associate vs Quality Control Inspector?

AspectQuality Assurance AssociateQuality Control Inspector
CertificationsOften requires certifications like ASQ CQIA or related quality assurance trainingMay require certifications such as ISO auditor or specific industry standards
Work EnvironmentInvolves process audits, documentation, and improving quality systemsFocuses on inspecting products or materials for defects
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and tech industriesPrimarily in manufacturing, food production, and assembly lines

While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.

Is a Quality Assurance Associate an entry-level job?

A Quality Assurance Associate position is often considered entry-level, suitable for candidates with little to no prior experience in quality assurance or related fields. It typically requires basic knowledge of testing procedures, attention to detail, and may involve training on specific tools or software used in quality control processes.

What is the role of a quality assurance associate?

A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What are the most commonly searched types of Quality Assurance jobs in Iowa?

The most popular types of Quality Assurance jobs in Iowa are:

What are popular job titles related to Quality Assurance Associate jobs in Iowa?

For Quality Assurance Associate jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Quality Assurance Associate jobs in Iowa look for?

The top searched job categories for Quality Assurance Associate jobs in Iowa are:

What cities in Iowa are hiring for Quality Assurance Associate jobs?

Cities in Iowa with the most Quality Assurance Associate job openings:

Quality Assurance Associate jobs near you
Infographic showing various Quality Assurance Associate job openings in Iowa as of August 2026, with employment types broken down into 2% As Needed, 80% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $57,224 per year, or $27.5 per hour.

Quality Assurance Engineer

Perspective Therapeutics, Inc.

Coralville, IA • On-site

Full-time

Posted 15 days ago

Job description

Objective
The Quality Assurance Engineer provides Quality oversight activities for the aseptic fill/finish manufacturing suite. Provide Quality Assurance technical expertise to ensure aseptic manufacturing facility, processes and support systems are in compliance with company guidelines and CGMP regulations, manufactured products and/or their raw materials, APIs, excipients or components.Essential Functions
  • Collaborate with full range of personnel in manufacturing, facilities, inventory, quality control and assurance, supply chain, animal resources, and technical work teams that support Production to identify root cause of a problem and determine appropriate corrective action for investigations.
  • Consult with a range of internal and external clients to correct non-routine and, or comprehensive issues, identify trends and determine corrective actions. Make recommendations that meet technical, regulatory and business requirements.
  • Perform batch issuance, review and release of clinical drug products and associated records.
  • Provide technical expertise in conducting investigations and make recommendations for targeted data and information collection as required for quality events. Contribute to data and information collection and statistical analysis.
  • Alert management of critical issues that have significant impact related to manufacturing objectives and timelines.
  • Develop, review and approve qualification/validation protocols and reports for facilities, utilities, equipment, processes and systems.
  • Analyze qualification/validation data to ensure compliance with statistically sound, predefined acceptance criteria.
  • Create and Update Quality Assurance and Quality Systems policies and Standard Operating Procedures (SOPs) to ensure compliance to CGMPs.
  • Review validation reports, summarizing findings and providing recommendations for improvements.
  • Conduct cross-functional risk assessments to identify potential quality and compliance issues.
  • Implement and monitor risk mitigation strategies throughout the qualification/validation lifecycle.
  • Ensure all qualification/validation activities comply with relevant regulatory standards.
  • Maintain accurate and comprehensive documentation to support regulatory submissions and audits.
  • Lead and approve change controls related to and represent Quality in Change Control Board meetings as needed.
  • Represent QA in a range of team meetings, processes and initiatives both internally and externally.
  • Provide quality oversight support for regulated operations, including review of documentation, compliance monitoring, and QA surveillance activities, as applicable.
  • Actively promote safety rules and awareness. Demonstrate good safety practices at all times including the appropriate use of protective equipment. Report and take initiative to correct safety & environmental hazards.
  • Handling of and/or exposure to potentially hazardous chemical, radiological and/or biological materials. Required to follow all safety procedures and use personal and protective equipment provided.
  • Other duties as required.
Education/Experience
  • BS/BA degree in a scientific discipline with 3-5+ years of progressive experience in the pharmaceutical or radiopharmaceutical industry or related GMP environment, or equivalent.
  • 1-2+ years of experience in quality assurance and qualification/validation within a regulated industry (e.g., pharmaceuticals, medical devices, biotechnology).
  • Aseptic fill-finish experience, including familiarity with qualification/validation of aseptic manufacturing technologies and facilities is required.
  • Understanding of regulatory requirements and quality standards in the pharmaceutical industry preferred.
  • Understanding of risk management, quality by design principles, statistical analysis (DOE, SPC, ANOVA, etc...)

Knowledge/Skill/Ability
  • Ability to work in a team-oriented environment and represent the Quality organization on multi-disciplinary teams.
  • Knowledge and experience with GMP, GLP, and GCP requirements.
  • Knowledge of corporate governance, health care regulations, laws, and standards.
  • Strong understanding of quality management systems and (GxP), to ensure compliance with regulatory requirements.
  • Understanding of Facilities, Utilities, and Equipment Qualification and Computer System Validation Assurance requirements.
  • Ability to adapt quickly in a fast-paced dynamic environment.
  • Ability to communicate with and positively influence broad and diverse populations within and outside the organization.
  • Ability to work in a team environment with minimum supervision.
  • Strong collaborative, partnering, and interpersonal skills.
  • Excellent communication skills, both written and oral.
  • High ethical standards, trustworthy, operating with absolute discretion.
  • Highly organized with great attention to detail.
  • Flexibility to work various shifts, as required.
  • Ability to lift up to 50 pounds, to and from a mobile cart, utilizing proper lifting and movement techniques.
  • Travel up to 10% may be required.
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
During the course of this job, the employee may encounter exposure to radiation hazards.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

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