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Cvs Qa Jobs (NOW HIRING)

Perrigo Company plc

QA Technician - 2nd

Holland, MI · On-site

Scope of the Role The QA Technician responds to quality events, completes related documentation ... and CVs, must be submitted in English. Thank you. We are an equal opportunity employer. All ...

Perrigo

QA Technician - 2nd

Holland, MI

Scope of the Role The QA Technician responds to quality events, completes related documentation ... and CVs, must be submitted in English. Thank you. We are an equal opportunity employer. All ...

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 ...

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 ...

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How much do cvs qa jobs pay per hour?

As of May 29, 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 job?

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, and why are they important?

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 May 2026, with employment types broken down into 1% As Needed, 90% Full Time, and 9% Part Time. Highlights an 74% Physical, and 26% Remote job distribution, with an average salary of $91,156 per year, or $43.8 per hour.

Quality Assurance Associate

Lupin Pharmaceuticals Inc.

Coral Springs, FL • On-site

Full-time

Posted 26 days ago

Job description

Overview
Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way.
Responsibilities
Role Summary
Quality Assurance Associate independently performs tasks with minimal supervision ensuring compliance with LIRC Quality Assurance programs and procedures, and all applicable predicate rules. Assists in the maintenance of Quality Systems and develops new controls and procedures that are appropriate and effective as part of continuous Quality Improvement activities at the site. Ensures that Laboratory and Manufacturing functions are operating in full compliance with the Current Good Manufacturing Practices (cGMPs), regulatory requirements, company procedures and continuous improvement.
This position will require flexibility to work between 1st and 2nd shift - but will lean heavier to 2nd Shift. 3:00 p.m. - 11:00 p.m.
Essential Duties and Responsibilities
  • Participate in the design and development of Lupin's Quality Systems and provide support of continuous improvement and management of Quality Systems.
  • Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc.
  • Release of cleanrooms after cleaning activities.
  • Inspection and release of GMP area prior to manufacturing activities.
  • Inspection of incoming materials, in process and finished products.
  • Provide support in the review of cGMP documentation, including, but not limited to specifications, standard operating procedures/ test methods, and batch records.
  • Support internal and to 3rd party audits at LIR site.
  • Facilitate quality-related training and mentoring, where required.
  • Partnership with other functional areas (Operations, Product Development, Quality Control, Engineering and Facilities, Manufacturing, and Supply Chain) to ensure site continuous compliance.
  • Support employee training program.
  • Management of QA retain samples and archival of GMP documents.
  • Provide support in the documentation of investigations and Root Cause Analysis.
  • Perform other QA duties as assigned.

Qualifications
Education & Experience
  • A Bachelor's Degree (B.S.) in Chemistry, Biology, Microbiology or Pharmacy related field is preferred.
  • A minimum of 1-3 years' experience in an FDA-regulated or Pharmaceutical/Medical Device manufacturing environment.
  • A thorough knowledge of cGMP regulations as they apply to Drugs and Medical Devices is required. Relevant experience with laboratory and manufacturing functions along with GMP quality assurance functions is required.
  • Ability to enforce adherence to internal quality policies, procedures and cGMP.
  • Ability to interface and work with a diverse group of departments and individuals is required.
  • Must be team oriented with excellent interpersonal skills. Must have the ability to express regulatory requirements clearly and understandably.
  • Must possess good oral and written skills in the English language.
  • Availability to work in second shift.

Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran's status, or any other classification as required by applicable law.
Physical Requirements
The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally work is performed in an office environment.
Search Firm Representatives Please Read Carefully
Lupin USA, and its Affiliates does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms for any current openings at our company without a valid written search agreement in place will be deemed the sole property of Lupin. No fee will be paid in the event a candidate is hired by Lupin as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, No phone calls or emails

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