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Quality Assurance In Pharmaceutical Jobs (NOW HIRING)

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing ... Quality Assurance Engineer Location: Tampa, FL - 33634 Duration: 12 months Job Type: Temporary ...

Cipla

QA Inspector I - 1st Shift

Fall River, MA · On-site

$23 - $30/hr

Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES

Cipla

QA Inspector I - 3rd Shift

Fall River, MA · On-site

$23 - $30/hr

Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES

Cipla

QA Inspector I - 1st Shift

Fall River, MA · On-site

$23 - $30/hr

Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES

Cipla

QA Inspector I - 3rd Shift

Fall River, MA · On-site

$23 - $30/hr

Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. * Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES

Cipla

$23 - $30/hr

Minimum of two (2) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...

Cipla

$23 - $30/hr

Minimum of two(2) years' experience in quality assurance in a GMP pharmaceutical manufacturing ... operation and work environment. Experience in MDI preferred. KNOWLEDGE, SKILLS, AND ABILITIES ...

Alkermes

Product Quality Lead

Waltham, MA · On-site

... Quality Assurance in support of pharmaceutical development operations. * Ability to be main point of contact and interact effectively in relation to on-site cGMP audits by external auditors.

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How much do quality assurance in pharmaceutical jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for quality assurance in pharmaceutical in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

What is the highest salary in QA Pharma?

The highest salaries for Quality Assurance professionals in the pharmaceutical industry can reach over $120,000 annually, especially for senior roles with extensive experience, advanced certifications, and leadership responsibilities. Salaries vary based on location, company size, and individual expertise, with top earners often working in major pharmaceutical hubs and holding specialized skills in GMP compliance and validation.

What does quality assurance do in pharma?

In pharmaceutical quality assurance, professionals ensure that manufacturing processes and products meet regulatory standards and company quality policies. They conduct audits, review documentation, and implement procedures to prevent defects and ensure product safety and efficacy. QA specialists often use tools like GMP guidelines and may hold certifications such as CQE or CQA.

Does QA or QC pay more?

In pharmaceutical quality assurance (QA) and quality control (QC) roles, QA positions often have higher salaries due to their focus on process improvement, compliance, and documentation, while QC roles typically involve laboratory testing and inspection. Salary differences can vary based on experience, certifications, and location, but generally, QA roles tend to pay more than QC roles in the industry.

Is quality assurance in pharma a good career?

Quality assurance in pharmaceutical is a stable and growing career that involves ensuring products meet safety and quality standards, often requiring knowledge of Good Manufacturing Practices (GMP) and quality management systems. It offers opportunities for advancement, certifications, and a role in public health, making it a valuable profession for those interested in the industry.

What are some common challenges faced by Quality Assurance professionals in the pharmaceutical industry, and how can they be effectively managed?

Quality Assurance (QA) professionals in the pharmaceutical industry often face challenges such as keeping up with evolving regulatory requirements, ensuring consistent documentation, and coordinating cross-functional teams during audits. Managing these challenges requires continuous training, strong attention to detail, and effective communication skills. Collaboration with other departments, such as production and regulatory affairs, is key to identifying issues early and maintaining compliance with Good Manufacturing Practices (GMP). Establishing clear quality procedures and staying proactive with process improvements also help QA professionals maintain high standards and reduce risks.

What are the key skills and qualifications needed to thrive as a Quality Assurance professional in the pharmaceutical industry, and why are they important?

A successful Quality Assurance professional in pharmaceuticals needs a solid background in life sciences or pharmacy, understanding of GMP regulations, and relevant QA experience. Familiarity with quality management systems (QMS), documentation software, and regulatory compliance tools is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for excelling in this role. These skills ensure product safety, regulatory compliance, and the consistent delivery of high-quality pharmaceutical products.

What does a Quality Assurance professional do in the pharmaceutical industry?

A Quality Assurance (QA) professional in the pharmaceutical industry is responsible for ensuring that all products meet established standards of quality, safety, and efficacy. They develop, maintain, and monitor procedures and systems that comply with regulatory requirements such as Good Manufacturing Practices (GMP). QA professionals conduct audits, review documentation, manage deviations, and support continuous improvement to ensure that medications are safe for patients. Their work is critical in preventing errors, ensuring product consistency, and maintaining the trust of regulatory agencies and consumers.

What is the difference between Quality Assurance In Pharmaceutical vs Quality Control In Pharmaceutical?

AspectQuality Assurance In PharmaceuticalQuality Control In Pharmaceutical
FocusProcesses, compliance, and preventing defectsTesting and inspecting products for defects
ResponsibilitiesDeveloping quality systems, audits, documentationSampling, testing, and analyzing products
CredentialsGMP certifications, quality management trainingLab certifications, analytical testing skills
Work EnvironmentOffice-based, quality departments, manufacturing sitesLaboratories, manufacturing facilities

Quality Assurance In Pharmaceutical focuses on establishing and maintaining quality systems to prevent issues, while Quality Control In Pharmaceutical emphasizes testing products to identify defects. Both roles are essential in ensuring pharmaceutical safety and compliance, but they differ in scope and daily tasks.

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Quality Assurance In Pharmaceutical jobs near you
QA Auditing Reviewer

QA Auditing Reviewer

Amneal Pharmaceuticals LLC

Piscataway, NJ

$23 - $32/hr

Full-time

Medical, Retirement

Posted 29 days ago

Amneal Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

57th of 74 rated pharmaceutical

Job description

Description:

This QA Auditing Reviewer role is responsible for thoroughly auditing production records, determining batch disposition (Release, Hold, Reject), and executing those decisions in systems like JDE while ensuring held or rejected batches are properly controlled and stored. It also logs and loads batch data into required databases, regularly audits QA inprocess data, and may fill in for inprocess QA inspectors when needed.


Essential Functions:

  • Thoroughly audit all production records (work order #1 and #2 for commercial and exhibit batches) and determine batch disposition (Release, Hold, Reject). Physically perform batch disposition for each lot of product produced, including making the correct entries in JDE.
  • Responsible for making sure Batches placed on Hold or Reject status are appropriately stored in their designated limited access areas.
  • Log RFT data in accordance with established QA Processes
  • Load batch data into the APR database (if required)
  • Communicating clearly and concisely, both orally and in writing.
  • Operating scientific calculators and personal computers
  • Performs timely reviews of QA In-Process Data


Additional Responsibilities:

  • Must be able to fill in for In-process QA inspectors when needed

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com. Requests will be handled confidentially and in accordance with applicable laws. 


Education:

  • High School or GED - Required
  • Bachelors Degree in Related Field - Preferred

Experience:

  • 2 years or more in Pharmaceutical QA, QC or QM

Specialized Knowledge:

  • Excellent knowledge of manufacturing processes from Raw Material Receipt through finished goods packaging
  • Comprehensive understanding of GMP standards, including 21 CFR Parts 210, 211, 820, and relevant ICH guidance.

The hourly rate for this position ranges from $23.00-$32.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.

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