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Quality Assurance Qa Associate Jobs (NOW HIRING)

Tailstorm Health Inc

QA Associate

Chandler, AZ · On-site

$45K/yr

Position Summary The Quality Assurance Associate - Document Control & Compliance is responsible for supporting document control, customer qualification, regulatory compliance, and record management ...

Alcon3Pl

QA Associate - Livermore, CA

Livermore, CA · On-site

$26 - $30/hr

QA Associate - Livermore, CA Lobos Staffing is hiring a QA Associate for a temp-to-perm opportunity in Livermore, CA. Schedule: Monday-Friday, 7:00 AM-3:30 PM Pay: $26-$30/hour, DOE Must be available ...

Linde

Quality Assurance Associate

Phoenix, AZ · On-site

Quality Assurance Associate Phoenix, AZ, United States req32255 Work Schedule: 1st Shift What you will enjoy doing* * Support and lead quality investigations involving defects, non-conformances ...

ANI Pharmaceuticals

QA Associate

East Windsor, NJ · On-site

$52K - $70K/yr

Quality Standards and Best Practices * Rules and Regulations Minimum Experience * 5 years' experience in Quality Assurance Minimum Field of Expertise * Computer skills * Previous work in a regulated ...

Via Logic LLC

Quality Assurance (QA) Lead

Chantilly, VA · On-site

$92K - $166K/yr

The QA Lead will be responsible for developing and implementing quality standards and procedures to ensure compliance with customer expectations, contractual obligations, and applicable regulatory ...

SynQor

Quality Assurance (QA) Inspector

Salem, NH · On-site

$19 - $22/hr

Description The Quality Assurance (QA) Inspector will provide support to the SMT, Through Hole, and Systems Integration processes. The QA Inspector will perform product quality control inspections ...

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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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Quality Assurance Qa Associate jobs near you
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 Associate

Pittsburgh, PA • On-site

Krystal Biotech
Biotechnology Research and Development • 51 - 200 employees
Learn more about Krystal Biotechexternal

Full-time

Re-posted 13 days ago

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 headquarters in Pittsburgh's South Side.
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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