Top 51 Quality assurance director Jobs in New Jersey

Associate Director, Quality Assurance (Clinical Research Preferred)
IQVIA —Wayne, NJ
- $88,600 - $246,600 a year
- Full-time
- Remote
- Nursing
- Bachelor's degree
- Mentoring
- Work from home
Site Quality Director (Somerset New Jersey)
Ardena —Somerset, NJ
- $200,000 - $220,000 a year
- Hybrid work
- Bachelor of Science
- 11+ years
- Bachelor's degree
Executive Director of Quality Assurance
SystImmune —Princeton, NJ
- $240,000 - $300,000 a year
- Full-time
- Hybrid work
- Nursing
- Office
- Bachelor's degree
- Paid holidays
- Disability insurance
16h
Director, PV QA DSI
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $184,240 - $276,360 a year
- Master's degree
- Bachelor's degree
- Mentoring
Director, Quality Systems Global
Balchem Corporation —Montvale, NJ
- $170,000 - $180,000 a year
- Full-time
- Hybrid work
- 7 years
- Analysis skills
- Senior level
Quick Apply
Director, Quality Assurance
Avet Pharmaceutical —E Brunswick, NJ
- $170,000 - $200,000 a year
- Full-time
- English
- Office
- Supervising experience
- Paid holidays
- Health insurance
Quick Apply
Director - Quality Assurance
Thea Energy —Kearny, NJ
- $180,000 - $225,000 a year
- Weekends as needed
- OSHA
- Ability to lift 50 pounds
- Travel
- Health insurance
- Dental insurance
Quick Apply
Associate Director, Quality Assurance-Hospice
BAYADA Home Health Care —Pennsauken, NJ
- $110,000 - $114,000 a year
- Remote
- Microsoft Word
- 7 years
- RN License
Quick Apply
Director, GCP Quality Inspection Management
SK Life Science, Inc. —Paramus, NJ
- $180,000 - $220,000 a year
- Full-time
- Master's degree
- Bachelor's degree
- Training & development
- Health insurance
- Dental insurance
Quality Assurance Director - GMP ESO Biotechnologies
Recordati —Bridgewater, NJ
- $149,160 - $223,740 a year
- Weekends as needed
- Hybrid work
- 11+ years
- English
- Office
- AD&D insurance
- Paid holidays
Director of Quality Assurance - Bergen/Essex/Hudson/Passaic/Union Counties
Allies, Inc. —New Jersey
- Full-time
- Clean driving record
- Management
- Office
- Paid holidays
- Disability insurance
Director, Quality
Catalent —Princeton, NJ
- $190,000 - $230,000 a year
- Email
- Engineering
- Organizational skills
- In-person
- Paid holidays
- Health insurance
QA Manager/Associate Director – Quality Assurance (Job Code: QA)
Primera Analytical Solutions —Princeton, NJ
- 5 years
- Bachelor of Science
- Bachelor's degree
8d
Director, Clinical Quality Assurance (GCP)
Eikon Therapeutics —Jersey City, NJ
- $204,000 - $246,750 a year
- Up to 50% travel
- 11+ years
- Office
- AD&D insurance
- Paid holidays
Quick Apply
Director, Enterprise Quality Engineering
Humana —New Jersey
- $156,600 - $215,400 a year
- Full-time
- Remote
- 5 years
- Travel
- Organizational skills
- Paid parental leave
- Paid holidays
Director, Corporate Quality Management System (QMS)
Integra LifeSciences —Princeton, NJ
- $166,750 - $228,850 a year
- Email
- Engineering
- 11+ years
- Office
- Disability insurance
- Health insurance
Director, Quality Systems (SM)
BD —Franklin Lakes, NJ
- $211,900 - $339,000 a year
- Bachelor of Science
- Office
- Bachelor's degree
4d
Director, Quality Compliance
Cellares —Bridgewater, NJ
- $90,000 - $250,000 a year
- Full-time
- 5 years
- Mentoring
- Senior level
- Health insurance
- Dental insurance
Senior Director, Supplier & External Manufacturing Quality
Integra LifeSciences —Princeton, NJ
- $192,050 - $263,350 a year
- Email
- Engineering
- 11+ years
- Master's degree
- Disability insurance
- Health insurance
Director, Product Quality Lead
Kardigan —Princeton, NJ
- $194,000 - $250,000 a year
- 11+ years
- Bachelor's degree
- Senior level
3d

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Associate Director, Quality Assurance (Clinical Research Preferred)

IQVIA -
Wayne, NJ

Apply Now

Job Details

Full-time
$88,600 - $246,600 a year

Benefits

Work from home

Qualifications

Customer communication

Full Job Description

Wayne, United States of America | Full time | Home-based | R1557774

Job Overview

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

quality assurance director jobs in new jersey

Associate Director, Quality Assurance (Clinical Research Preferred)

Site Quality Director (Somerset New Jersey)

Executive Director of Quality Assurance

Director, PV QA DSI

Director, Quality Systems Global

Director, Quality Assurance

Director - Quality Assurance

Associate Director, Quality Assurance-Hospice

Director, GCP Quality Inspection Management

Quality Assurance Director - GMP ESO Biotechnologies

Director of Quality Assurance - Bergen/Essex/Hudson/Passaic/Union Counties

Director, Quality

QA Manager/Associate Director – Quality Assurance (Job Code: QA)

Director, Clinical Quality Assurance (GCP)

Director, Enterprise Quality Engineering

Director, Corporate Quality Management System (QMS)

Director, Quality Systems (SM)

Director, Quality Compliance

Senior Director, Supplier & External Manufacturing Quality

Director, Product Quality Lead

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