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Cvs Qa 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

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 ...

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How much do cvs qa jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for cvs qa in the United States is $43.83, according to ZipRecruiter salary data. Most workers in this role earn between $38.70 and $47.84 per hour, depending on experience, location, and employer.

What is a CVS QA?

A CVS QA (Quality Assurance) job typically involves ensuring the quality and accuracy of pharmacy operations, software systems, or customer service processes within CVS Health. Responsibilities may include testing and identifying issues in digital platforms, verifying compliance with company and regulatory standards, and collaborating with teams to improve workflows. The role requires attention to detail, problem-solving skills, and knowledge of QA methodologies. Depending on the focus area, CVS QA professionals may work in pharmacy quality assurance, software testing, or operational audits.

What are the key skills and qualifications needed to thrive in the CVS QA position?

To excel as a CVS QA (Computerized Validation System Quality Assurance) professional, a solid background in quality assurance, computer system validation, and regulatory compliance (such as FDA or GxP) is essential. Familiarity with validation life cycle documentation, risk assessment tools, and systems like SAP, TrackWise, or other quality management systems, as well as certifications like ASQ or ISPE, are highly valued. Strong analytical thinking, attention to detail, and effective communication skills are important for collaborating with cross-functional teams and ensuring thorough documentation. These capabilities ensure that computerized systems comply with industry standards, avoid regulatory risks, and support the integrity of pharmaceutical or biotech operations.

What are the primary challenges faced by CVS QA professionals in their daily work?

CVS QA professionals often face the challenge of keeping up with ever-evolving regulatory requirements and ensuring all computerized systems within the organization remain compliant. They must meticulously review and document validation activities while coordinating with IT, operations, and QA teams to resolve issues or discrepancies. Effective prioritization and problem-solving are crucial, as projects frequently have tight deadlines and require balancing multiple systems simultaneously. Successfully managing these challenges not only ensures regulatory compliance but also contributes to maintaining patient safety and data integrity.

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Cvs Qa jobs near you
Infographic showing various Cvs Qa job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 4% Part Time, 6% Contract, and 1% Nights. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $91,156 per year, or $43.8 per hour.

Quality Assurance Associate

Krystal Biotech

Moon Township, PA • On-site

Full-time

Re-posted 21 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.

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