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Quality Assurance Qa Associate Jobs (NOW HIRING)

Quality Assurance Associate Minimize monetary loss of defective merchandise by identifying the most effective defect recovery process for each item. Essential Duties and Responsibilities include the ...

Quality Assurance Associate Minimize monetary loss of defective merchandise by identifying the most effective defect recovery process for each item. Essential Duties and Responsibilities include the ...

The Quality Assurance Associate must demonstrate a high level of individual responsibility and accountability and possess the ability to perform to the requirements listed below. The QA Associate ...

The Quality Assurance Associate will ensure each center process adheres to all federal, local, and organizational standards related to the collection and manufacturing of human blood plasma. On-site ...

Job Title: QA Associate (Quality Assurance) Location:Pomona, CA (In-office) Position Type:Full-time Vacancy Status:This position is vacant AI Disclosure in Hiring:We use artificial intelligence to ...

Pomona, CA,United States | Full-time regular Job Title: QA Associate (Quality Assurance) Location: Pomona, CA (In-office) Position Type: Full-time Vacancy Status: This position is vacant AI ...

The Quality Assurance Associate must demonstrate a high level of individual responsibility and accountability and possess the ability to perform to the requirements listed below. The QA Associate ...

We are looking for a Quality Assurance Associate to join a high-tech pharm/biotech environment in Middleton, Wisconsin. This Long-term Contract position is well suited for an early-career quality ...

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Quality Assurance Qa Associate information

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How much do quality assurance qa associate jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for quality assurance qa associate in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What does a quality assurance QA associate do?

A Quality Assurance (QA) Associate is responsible for ensuring that products or services meet established quality standards and regulatory requirements. They develop and implement testing procedures, conduct inspections, and identify areas for improvement in production or service processes. QA Associates work closely with other departments to resolve quality-related issues and help maintain compliance with company policies and industry regulations. Their work is essential for delivering consistent, safe, and effective products to customers.

How does a quality assurance QA associate typically interact with other departments to ensure product quality?

Quality Assurance QA Associates frequently collaborate with teams such as Production, Research & Development, and Regulatory Affairs to uphold product quality standards. They review documentation, provide feedback on process improvements, and may participate in cross-functional meetings to address quality concerns or deviations. This teamwork is essential for identifying potential issues early, ensuring compliance with regulations, and supporting a culture of continuous improvement throughout the organization.

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

To thrive as a Quality Assurance QA Associate, you need a strong understanding of quality control processes, documentation standards, and often a degree in a scientific or technical field. Familiarity with quality management systems (such as ISO standards), proficiency in data analysis tools, and experience with software like LIMS or ERP systems are typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for this position. These skills ensure products meet regulatory requirements and company standards, ultimately protecting consumer safety and business reputation.

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

AspectQuality Assurance Qa AssociateQuality Control Inspector
Primary FocusPreventing defects through process improvementsDetecting defects in finished products
Work EnvironmentCollaborates with teams, audits, documentationInspects products on production lines or in labs
CertificationsOften requires QA certifications, ISO standards knowledgeMay require specific industry certifications, safety training
Industry UsageCommon in manufacturing, software, healthcarePrimarily in manufacturing, food, electronics

The main difference is that a Quality Assurance Qa Associate focuses on preventing defects through process improvements and audits, while a Quality Control Inspector primarily detects defects in finished products. QA associates work proactively to ensure quality standards are met, whereas QC inspectors verify product quality after production. Both roles are essential in maintaining product standards but serve different points in the quality management process.

Is a Quality Assurance Qa Associate an entry level job?

A Quality Assurance QA Associate is often an entry-level position that requires basic knowledge of testing processes, attention to detail, and familiarity with tools like test management software. Many employers provide on-the-job training, and the role typically does not require extensive prior experience or advanced certifications.
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Infographic showing various Quality Assurance Qa Associate job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

Quality Assurance (QA) Associate

Cincinnati, OH • On-site

Medpace, Inc.
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

Full-time

Medical, Retirement, PTO

Re-posted 25 days ago


Key responsibilities

  • Facilitate Medpace sponsor audits onsite and manage pre-inspection activities.

  • Review and assess responses to sponsor audit reports and provide guidance during audits.

  • Manage inspection backroom during regulatory inspections and conduct inspection readiness activities.


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz


Job description

Job Summary

The successful candidate will be responsible for facilitating the management of sponsor audits, broad range of regulatory inspections (FDA, EMA, MHRA) and facilitating QA relationship with external clients. The position will also include conducting inspection readiness activities for Medpace and Medpace stakeholders.

Responsibilities
  • Facilitating Medpace sponsor audits onsite;
  • Review and assess responses to sponsor audit reports;
  • Provide clarity to the Quality Management System (QMS) during sponsor audits and other external audits;
  • Provide guidance to Medpace study teams during sponsor audits;
  • Manage pre-inspection activities for Medpace inspections;
  • Provide inspection data trends to the Quality Metrics group for executive management review;
  • Manage the inspection backroom during regulatory inspections to facilitate the timely delivery of requested documents;
  • Conduct mock interviews for subject matter experts (SMEs) during inspection preparation;
  • Reviewing, and analyzing regulatory inspection data issued by regulatory authorities (e.g. MHRA, EMA, FDA);
  • Manage training for Medpace stakeholders with respect to inspection readiness;
  • Conducting inspection readiness visits at selected sites (as applicable) to assess inspection risk;
  • Act as QA lead for inspections at Medpace;
  • Provide as needed support for inspections at Medpace external clients (sponsors and investigator sites); and
  • Maintain the memorializing of frequently asked questions repository for regulatory inspection.
Qualifications
  • Bachelor's degree in Life Sciences or a related field;
  • Experience in conducting and supporting regulatory inspections is a plus (FDA, MHRA and EMA);
  • Strong communication skills;
  • Strong quality mindset;
  • Experience in supporting or conducting audits;
  • Excellent written and verbal communications skills in English;
  • Independent thinking and planning ability;
  • Experience with a wide range of computerized systems;
  • Good time management skills;
  • Ability to switch between both big picture view and attention to detail; and
  • The ability to work well on a team as well as independently.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992