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Quality Assurance Qa Associate Jobs (NOW HIRING)

The QA Associate will need to provide support with identifying operational and quality gaps. The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing ...

The QA Associate will need to provide support with identifying operational and quality gaps. The Quality Assurance Associate will exemplify excellent interpersonal skills and be capable of developing ...

Job Title Quality Assurance Associate Job Category Quality JOIN OUR TEAM AS A QUALITY ASSURANCE ASSOCIATE At HYMH, we're committed to delivering the right part, to the right place, at the right time ...

Overview NOW HIRING - QUALITY ASSURANCE ASSOCIATE Kemin is seeking a full-time Quality Assurance Associate for our Missouri campus! Our Missouri campus consists of operations in both Verona and ...

Quality Assurance Associate (Entry-Level / Early Career) 🔬 Launch your career in quality and compliance with hands-on experience in a regulated environment About the Role We're looking for a ...

Century Group is partnering with a client that is seeking a Quality Assurance Associate to assist their team. Exact compensation may vary based on skills, experience, and location. Expected starting ...

We are seeking a detail-oriented Quality Assurance Associate to support our quality management system and help ensure products meet customer, regulatory, and internal standards. In this role, you ...

Overview NOW HIRING - QUALITY ASSURANCE ASSOCIATE Kemin is seeking a full-time Quality Assurance Associate for our Missouri campus! Our Missouri campus consists of operations in both Verona and ...

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Quality Assurance Qa Associate information

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$29

$62

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

As of Jun 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.

More about Quality Assurance Qa Associate jobs
What cities are hiring for Quality Assurance Qa Associate jobs? Cities with the most Quality Assurance Qa Associate job openings:
What are the most commonly searched types of Quality Assurance Qa jobs? The most popular types of Quality Assurance Qa jobs are:
What states have the most Quality Assurance Qa Associate jobs? States with the most job openings for Quality Assurance Qa Associate jobs include:
Infographic showing various Quality Assurance Qa Associate job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 98% Full Time, and 1% Part Time. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.
Quality Assurance (QA) Associate

Quality Assurance (QA) Associate

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, PTO

Posted 23 days ago


Medpace rating

8.4

Company rating: 8.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

15th of 57 rated research


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 science 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). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks

  • Cincinnati Campus Overview
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards

  • Named a Top Workplace in 2024 by The Cincinnati Enquirer

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Employment Type: OTHER

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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