ZipRecruiter

Log In

1

Cvs Quality Assurance Jobs (NOW HIRING)

U-Haul

Quality Assurance Analyst

Phoenix, AZ · On-site

Our team is looking for a Quality Assurance Analyst to join the U-Haul family. This person must be ... CVS Virtual Care * UHaul Kids Program * 24Hour Nurse Line * Wellness Program (Healthier You ...

U-Haul

Quality Assurance Analyst

Phoenix, AZ · On-site +1

Our team is looking for a Quality Assurance Analyst to join the U-Haul family. This person must be ... CVS Virtual Care * U-Haul Kids Program * 24-Hour Nurse Line * Wellness Program (Healthier You ...

U-Haul

Quality Assurance Analyst

Phoenix, AZ · Remote

As a QA Analyst, you will play a key role in ensuring the quality, reliability, and performance of ... CVS Virtual Care * UHaul Kids Program * 24Hour Nurse Line * Wellness Program (Healthier You ...

U-Haul

Quality Assurance Analyst

Phoenix, AZ · On-site

Our team is looking for a Quality Assurance Analyst to join the U-Haul family. This person must be ... CVS Virtual Care * U-Haul Kids Program * 24-Hour Nurse Line * Wellness Program (Healthier You ...

MicroCoders LLC

Entry level QA/BA

Reston, VA · On-site

MicroCoders LLC , is currently hiring Quality assurance analyst, and Business Analyst for ... CVS, Deutsche Bank, Disney, Eli Lilly, Freddie Mac, Fannie Mae, GMAC Insurance, IBM, ING Direct ...

MicroCoders LLC

Entry level QA/BA

Reston, VA

MicroCoders LLC , is currently hiring Quality assurance analyst, and Business Analyst for ... CVS, Deutsche Bank, Disney, Eli Lilly, Freddie Mac, Fannie Mae, GMAC Insurance, IBM, ING Direct ...

next page

Showing results 1-20

All JobsCvs Quality Assurance Jobs

Cvs Quality Assurance information

See salary details

$13

$22

$38

How much do cvs quality assurance jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for cvs quality assurance in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $25.72 per hour, depending on experience, location, and employer.

What is the difference between Cvs Quality Assurance vs Cvs Quality Control?

AspectCvs Quality AssuranceCvs Quality Control
FocusProcesses and procedures to prevent defectsDetection and correction of defects in products
ActivitiesAudits, process improvements, complianceInspections, testing, defect identification
CredentialsQuality certifications, industry standardsTesting certifications, technical skills
Work EnvironmentDocumentation, process managementLaboratory, production lines

While both roles aim to ensure product quality, Cvs Quality Assurance focuses on preventing defects through process improvements, whereas Cvs Quality Control emphasizes identifying and fixing defects through testing and inspections. Understanding these differences helps employers and job seekers target the right skills and responsibilities in the CVS industry.

What does a CVS Quality Assurance professional do?

A CVS Quality Assurance professional is responsible for ensuring that products and services in the pharmacy and retail environment meet established quality standards and regulatory requirements. They develop and implement quality control procedures, conduct audits, and address any issues related to compliance or safety. Their work helps maintain customer trust and ensures that products, such as medications and health products, are safe and effective for use. Additionally, they collaborate with other teams to improve processes and resolve any quality concerns promptly.

What are the key skills and qualifications needed to thrive as a CVS Quality Assurance professional?

To thrive as a CVS Quality Assurance professional, you generally need a strong background in quality management, knowledge of regulatory standards (such as GMP or ISO), and a relevant degree in pharmacy, life sciences, or a related field. Familiarity with quality management systems (QMS), auditing tools, and documentation software is typically required, along with certifications like ASQ or Six Sigma being advantageous. Attention to detail, analytical thinking, and effective communication are vital soft skills for identifying issues and working collaboratively with teams. These skills ensure the consistent delivery of safe, compliant, and high-quality products and services in a regulated environment.

What are some common challenges faced by CVS Quality Assurance professionals, and how are they typically addressed?

CVS Quality Assurance professionals often encounter challenges such as maintaining compliance with strict regulatory standards, identifying and resolving process inconsistencies, and ensuring clear communication across cross-functional teams. These challenges are typically addressed by staying up-to-date with industry regulations, implementing robust documentation practices, and participating in regular team meetings to align on quality goals. Building strong relationships with pharmacy staff and utilizing quality management systems also play a key role in proactively identifying and correcting quality issues.
More about Cvs Quality Assurance jobs
What cities are hiring for Cvs Quality Assurance jobs? Cities with the most Cvs Quality Assurance job openings:
What states have the most Cvs Quality Assurance jobs? States with the most job openings for Cvs Quality Assurance jobs include:
What job categories do people searching Cvs Quality Assurance jobs look for? The top searched job categories for Cvs Quality Assurance jobs are:
Cvs Quality Assurance jobs near you
Infographic showing various Cvs Quality Assurance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $47,496 per year, or $22.8 per hour.

Quality Assurance Associate

Krystal Biotech

Moon Township, PA • On-site

Full-time

Re-posted 11 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 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.

Apply