This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
The correct title for this position is Quality Sr. Scientist (Quality Assurance). Primarily focused ... Pharmaceutical quality standards. Performs testing including, but not limited to clinical and/or ...
The correct title for this position is Quality Sr. Scientist (Quality Assurance). Primarily focused ... Pharmaceutical quality standards. Performs testing including, but not limited to clinical and/or ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While ...
... of the world's best pharmaceutical, biotechnology and medical companies. As specialists in ... Experience in commercial quality assurance (marketed jobs, not just on the clinical and research ...
... of the world's best pharmaceutical, biotechnology and medical companies. As specialists in ... Experience in commercial quality assurance (marketed jobs, not just on the clinical and research ...
Quality Assurance Specialist
Clayton, IN · On-site
Knowledge of FDA 21 CFR Parts 111, 210 and 211 and applicable cGMP pharmaceutical quality requirements * Minimum of 3-5 years of Quality Assurance experience in a GMP-regulated pharmaceutical ...
Quick apply
Quality Assurance Specialist
Clayton, IN · On-site
Knowledge of FDA 21 CFR Parts 111, 210 and 211 and applicable cGMP pharmaceutical quality requirements * Minimum of 3-5 years of Quality Assurance experience in a GMP-regulated pharmaceutical ...
Quality Assurance Specialist
Clayton, IN · On-site
Knowledge of FDA 21 CFR Parts 111, 210 and 211 and applicable cGMP pharmaceutical quality requirements * Minimum of 3-5 years of Quality Assurance experience in a GMP-regulated pharmaceutical ...
Quality Assurance Specialist
Clayton, IN · On-site
Knowledge of FDA 21 CFR Parts 111, 210 and 211 and applicable cGMP pharmaceutical quality requirements * Minimum of 3-5 years of Quality Assurance experience in a GMP-regulated pharmaceutical ...
QA Product Manager (Sterile Products)
Florham Park, NJ · On-site
$120K - $150K/yr
Lead the Quality Assurance activities for sterile pharmaceutical products manufactured by third-party manufacturers including change controls, product quality incidents, deviations, non-conformances ...
QA Product Manager (Sterile Products)
Florham Park, NJ · On-site
$120K - $150K/yr
Lead the Quality Assurance activities for sterile pharmaceutical products manufactured by third-party manufacturers including change controls, product quality incidents, deviations, non-conformances ...
QA Product Manager (Sterile Products)
Florham Park, NJ · On-site
$120K - $150K/yr
Lead the Quality Assurance activities for sterile pharmaceutical products manufactured by third-party manufacturers including change controls, product quality incidents, deviations, non-conformances ...
QA Product Manager (Sterile Products)
Florham Park, NJ · On-site
$120K - $150K/yr
Lead the Quality Assurance activities for sterile pharmaceutical products manufactured by third-party manufacturers including change controls, product quality incidents, deviations, non-conformances ...
QA Product Manager (Sterile Products)
$120K - $150K/yr
Lead the Quality Assurance activities for sterile pharmaceutical products manufactured by third-party manufacturers including change controls, product quality incidents, deviations, non-conformances ...
QA Product Manager (Sterile Products)
$120K - $150K/yr
Lead the Quality Assurance activities for sterile pharmaceutical products manufactured by third-party manufacturers including change controls, product quality incidents, deviations, non-conformances ...
Sr. Manager QA, Quality Systems & Product Complaints
South San Francisco, CA · On-site
$165 - $225/hr
Medical
Dental
Vision
Life
Retirement
PTO
Career Opportunities with Rigel Pharmaceutical A great place to work. Join Our Team Share with ... QA, Q Systems & Product Complaints The Senior Manager, Quality Assurance, Quality Systems ...
Sr. Manager QA, Quality Systems & Product Complaints
South San Francisco, CA · On-site
$165 - $225/hr
Medical
Dental
Vision
Life
Retirement
PTO
Career Opportunities with Rigel Pharmaceutical A great place to work. Join Our Team Share with ... QA, Q Systems & Product Complaints The Senior Manager, Quality Assurance, Quality Systems ...
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Quick apply
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Senior Quality Assurance Specialist
Everett, WA · On-site
$91K - $125K/yr
Medical
Dental
Vision
Life
Retirement
PTO
Senior Quality Assurance Specialist TerraPower Isotopes is seeking an experienced Senior Quality ... Certification in a pharmaceutical Quality-related discipline, Lean Six Sigma or project management ...
New
Senior Quality Assurance Specialist
Everett, WA · On-site
$91K - $125K/yr
Medical
Dental
Vision
Life
Retirement
PTO
Senior Quality Assurance Specialist TerraPower Isotopes is seeking an experienced Senior Quality ... Certification in a pharmaceutical Quality-related discipline, Lean Six Sigma or project management ...
New
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...
Quality Assurance Specialist
New London, CT · On-site
$20 - $25/hr
Medical
Dental
Vision
Life
Retirement
PTO
Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic ...
Quality Assurance Specialist
New London, CT · On-site
$20 - $25/hr
Medical
Dental
Vision
Life
Retirement
PTO
Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic ...
The specialist oversees QA and technical documents according to FDA and other applicable regulatory ... pharmaceutical quality systems experience strongly preferred;
Quick apply
The specialist oversees QA and technical documents according to FDA and other applicable regulatory ... pharmaceutical quality systems experience strongly preferred;
Quality Assurance Specialist
$20 - $25/hr
Medical
Dental
Vision
Life
Retirement
PTO
Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic ...
Quality Assurance Specialist
$20 - $25/hr
Medical
Dental
Vision
Life
Retirement
PTO
Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic ...
Quality Assurance Specialist
New London, CT · On-site
$20 - $25/hr
Medical
Dental
Vision
Life
Retirement
PTO
Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic ...
Quick apply
Quality Assurance Specialist
New London, CT · On-site
$20 - $25/hr
Medical
Dental
Vision
Life
Retirement
PTO
Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic ...
Pharmaceutical Qa information
See salary details
$10.82 - $16.48
4% of jobs
$16.48 - $22.14
12% of jobs
$22.14 - $27.80
7% of jobs
$30.27 is the 25th percentile. Wages below this are outliers.
$27.80 - $33.46
4% of jobs
$33.46 - $39.12
6% of jobs
$39.12 - $44.78
7% of jobs
The median wage is $48.79 / hr.
$44.78 - $50.44
13% of jobs
$50.44 - $56.10
13% of jobs
$59.99 is the 75th percentile. Wages above this are outliers.
$56.10 - $61.76
13% of jobs
$61.76 - $67.42
15% of jobs
$67.42 - $73.08
6% of jobs
$10
$46
$73
How much do pharmaceutical qa jobs pay per hour?
What is a pharmaceutical QA?
Is pharmaceutical QA a good career?
What is the difference between Pharmaceutical Qa vs Pharmaceutical Quality Control Analyst?
| Aspect | Pharmaceutical Qa | Pharmaceutical Quality Control Analyst |
|---|---|---|
| Certifications | GMP, GDP, ISO certifications | GMP, GLP, ISO certifications |
| Work Environment | Quality assurance departments, regulatory compliance | Laboratories, testing facilities |
| Primary Focus | Ensuring quality processes and compliance | Testing and analyzing raw materials and products |
Pharmaceutical Qa professionals focus on maintaining quality standards through audits, documentation, and compliance, while Pharmaceutical Quality Control Analysts perform laboratory testing to verify product quality. Both roles are essential in the pharmaceutical industry and often work closely to ensure products meet regulatory requirements.
What are some common challenges faced by pharmaceutical QA professionals, and how can they be addressed?
What are the key skills and qualifications needed to thrive as a pharmaceutical QA, and why are they important?
How to become a pharmaceutical QA?
What cities are hiring for Pharmaceutical Qa jobs?
Cities with the most Pharmaceutical Qa job openings:
What are the most commonly searched types of Pharmaceutical Qa jobs?
The most popular types of Pharmaceutical Qa jobs are:
What states have the most Pharmaceutical Qa jobs?
States with the most job openings for Pharmaceutical Qa jobs include:
What job categories do people searching Pharmaceutical Qa jobs look for?
The top searched job categories for Pharmaceutical Qa jobs are:
- Pharmaceutical Quality Assurance Associate
- Manager Gmp Quality Assurance
- Pharmaceutical Quality Assurance Specialist
- Pharmaceutical Quality Manager
- Entry Level Quality Assurance Pharma
- Senior Pharmaceutical Quality Assurance Specialist
- Qa Compliance
- Pharmacovigilance Auditor
- Pharmaceutical Quality Control
- Executive Yahoo Quality Assurance

Full-time
Posted 15 days ago
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
62nd of 224 rated it services
Job description
Provide strategic quality leadership and oversight across assigned Quality Assurance (QA) programs, with a strong focus on clinical research, clinical operations, pharmaceutical development, and GxP-regulated activities. Influence quality outcomes across multiple functional areas, business units, and customer engagements through expert guidance, risk-based decision making, and oversight of quality systems and compliance programs.
Lead and coordinate QA initiatives supporting customer accounts, clinical and functional operations, audit and inspection readiness programs, and quality management systems at a regional and/or global level. Partner with stakeholders to assess and promote compliance with applicable regulatory requirements, industry guidelines, and company procedures while driving continuous improvement, risk mitigation, patient safety, and operational excellence.
This position is best suited for candidates with substantial Clinical Quality Assurance (CQA), GCP, GxP, pharmaceutical, biotechnology, CRO, healthcare, or clinical research experience. While experience supporting technology-enabled quality systems is valuable, candidates with a predominantly IT Quality Assurance background and limited exposure to regulated clinical environments may not possess the preferred qualifications for this role.
Essential Functions
- Serve as the primary QA liaison for assigned customers, sponsors, clinical operations groups, and internal functional areas.
- Provide Quality Assurance oversight and guidance of quality issues, deviations, CAPAs, risk assessments, and compliance initiatives.
- Serve as a subject matter expert in GCP, GxP, ICH guidelines, clinical trial regulations, and pharmaceutical quality requirements.
- Provide guidance, interpretation, training, and consultation regarding regulations, industry standards, corporate policies, and quality expectations to clinical and operational teams.
- Support inspection readiness activities and support responses to regulatory authority inspections, sponsor audits, and customer audits.
- Assist in the enhancement of Quality Assurance policies, procedures, and risk management programs by providing recommendations to regional and global QA leadership.
- Author, review, and maintain Quality Assurance Standard Operating Procedures (SOPs) and serve as a representative on global quality governance initiatives, if assigned.
- Support customer audits and regulatory inspections and support the development, implementation, and verification of corrective and preventive action (CAPA) plans.
- Support documentation, investigation, reporting, and resolution of compliance-related issues.
- Support Quality Management with proposal reviews, quality strategy development, and quality metric reporting.
- Analyze audit trends, compliance metrics, root causes, and quality indicators to identify opportunities for process improvement and risk reduction.
- Lead or participate in cross-functional quality improvement initiatives and strategic projects.
- Mentor, develop, and manage QA personnel while fostering a culture of quality, compliance, accountability, and continuous improvement.
Promote patient safety, data integrity, regulatory compliance, and quality excellence throughout the organization.
Qualifications
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, Healthcare Administration, Biology, Chemistry, or related scientific discipline, or equivalent combination of education and experience preferred
- Minimum of 10 years of Quality Assurance experience within pharmaceutical, biotechnology, CRO, medical device, healthcare, or clinical research environments.
- Demonstrated experience in GxP Quality Assurance,
- Strong knowledge of pharmaceutical research and development processes, clinical trial conduct, and global regulatory environments.
- Experience conducting audits, authoring audit reports, evaluating findings, and managing CAPA activities is an advantage.
- Proven ability to lead complex quality initiatives and influence stakeholders across multiple functions and organizational levels.
- Excellent problem-solving, risk assessment, negotiation, and decision-making skills.
- Strong organizational, communication, leadership, and team-building abilities.
- Experience managing multiple projects, priorities, timelines, and competing business needs.
- Ability to establish and maintain effective working relationships with customers, regulators, vendors, and internal stakeholders.
- Proficiency with Microsoft Office applications and quality management systems.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $88,600.00 - $246,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
About IQVIA
Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US