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Quality Associate Jobs in Pittsburgh, PA (NOW HIRING)

ConnectiveRx

Analyst, Operations QA

Pittsburgh, PA · On-site

Perform data analysis on data collected by Quality Associates to identify trends, insights, and areas of opportunity within programs and agent performance. Create slide decks and present these ...

New

System One

Quality Assurance Associate

Pittsburgh, PA · On-site

Tittle: Quality Assurance Associate Location : PA - Pittsburgh Mode : 5 days on site Duration : Contract to Hire Years Of Exp Required : 3+ Years Function of the Group: Testing for Teller ...

AccountStaff, Inc.

CSR QA Associate

Pittsburgh, PA · On-site

CSR QA Associate (Operations Quality Assurance) Join a quality-focused operations team where your evaluations directly improve customer experiences and program outcomes. As a CSR QA Associate ...

Quality Life Services

Medicaid Pending Associate

Butler, PA · On-site

$14.25 - $19/hr

Description Medicaid Pending Associate Opportunity at Quality Life Services Quality Life Services is seeking a Medical Pending Associate to join our team. The Medicaid Pending Associate is ...

Quality Life Services

Medicaid Pending Associate

Butler, PA · On-site

$14.25 - $19/hr

Description Medicaid Pending Associate Opportunity at Quality Life Services - Butler This is a Full-Time, in office position in Butler, PA Quality Life Services - Butler welcomes compassionate ...

Quality Life Services

Medicaid Pending Associate

Butler, PA · On-site

$14.25 - $19/hr

Medicaid Pending Associate Opportunity at Quality Life Services Quality Life Services is seeking a Medical Pending Associate to join our team. The Medicaid Pending Associate is responsible for ...

Oberg Industries

Quality Supervisor

Freeport, PA · On-site

Associate's or Bachelor's degree in Engineering, Quality Management, Manufacturing Technology, or related field (Associate degree with significant relevant experience considered). * Minimum 3-5 years ...

Oberg Industries

Quality Supervisor

Freeport, PA · On-site

Associate's or Bachelor's degree in Engineering, Quality Management, Manufacturing Technology, or related field (Associate degree with significant relevant experience considered). * Minimum 3-5 years ...

ATI

Quality Specialist

Washington, PA · On-site

Associates degree in a technical or engineering field, or minimum of five years work experience in ... Prior experience in a quality inspection role. Knowledge, Skills, and Abilities: * Detail-oriented

New

Seegrid

Quality Technician

Pittsburgh, PA · On-site

$16.50 - $22.25/hr

The Quality Technician must execute all Quality Control Standard operating procedures, work ... Minimum Associate Degree or technical school degree in Mechanical/Electrical Engineering, Electro ...

Seegrid

Quality Technician

Pittsburgh, PA · On-site

$16.50 - $22.25/hr

The Quality Technician must execute all Quality Control Standard operating procedures, work ... Minimum Associate Degree or technical school degree in Mechanical/Electrical Engineering, Electro ...

Seegrid

Quality Technician

Pittsburgh, PA · On-site

$16.50 - $22.25/hr

The Quality Technician must execute all Quality Control Standard operating procedures, work ... Minimum Associate Degree or technical school degree in Mechanical/Electrical Engineering, Electro ...

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All JobsQuality Associate JobsQuality Associate Jobs in Pittsburgh, PA

Quality Associate information

See Pittsburgh, PA salary details

$10

$26

$49

How much do quality associate jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for quality associate in Pittsburgh, PA is $26.15, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $30.58 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

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

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Pittsburgh, PA?

The most popular types of Quality jobs in Pittsburgh, PA are:

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For Quality Associate jobs in Pittsburgh, PA, the most frequently searched job titles are:

What job categories do people searching Quality Associate jobs in Pittsburgh, PA look for?

The top searched job categories for Quality Associate jobs in Pittsburgh, PA are:

What cities near Pittsburgh, PA are hiring for Quality Associate jobs?

Cities near Pittsburgh, PA with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Pittsburgh, PA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $54,384 per year, or $26.1 per hour.

Quality Assurance Associate

Krystal Biotech

Moon Township, PA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

About Krystal Bio:
At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Job Description Summary:
Krystal Biotech, Inc. is seeking a highly motivated and experienced Quality Associate to support quality systems, GMP manufacturing processes and documentation practices at our Astra manufacturing facility in Moon Township, PA.
Primary Responsibilities:
  • Work with internal teams to obtain an understanding of the product and the documentation requirements.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended use.
  • Develop expertise on FDA regulations and audit processes.
  • Initiate and update GMP manufacturing associated documentation, such as clearing procedures.
  • Provide oversight of daily QA functions which include review and approval of records generated by manufacturing and quality control documents.
  • Provide support for updates on standard operating procedures and associated forms.
  • Assist with QA efforts for site cGXP documentation related to the operation of gene therapy manufacturing.
  • Ensure compliance with regulatory agencies and oversee continuous improvement of company's QA and compliance functions.
Requirements & Desired Competencies:
  • Minimum of a Bachelor's Degree (Biology or related Life Science) with 3+ years of relevant quality systems experience in the biotech or pharmaceutical industry.
  • Background that includes knowledge/experience in GMP, GLP, and GCP.
  • Experience with FDA audits is highly preferred.
  • Strong knowledge of GMP and ICH requirements.
  • Must be a self-starter and capable of working with minimal oversight.
  • Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately.
  • Excellent oral and written communication skills.

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.

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