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Manager, Quality Assurance

IQVIA

Durham (NC)

On-site

USD 90,000 - 130,000

Full time

30+ days ago

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Job summary

A leading global provider of clinical research services is seeking a Quality Assurance Manager in Durham, NC. You will oversee and coordinate QA programs supporting customer accounts and ensure compliance with regulatory standards. The ideal candidate should have at least 7 years of QA experience and strong leadership skills.

Benefits

Comprehensive benefits programs
Support for physical, mental, and emotional well-being

Qualifications

  • Minimum 7 years of QA experience in pharmaceutical or related area.
  • Minimum 5 years of management experience.
  • Equivalent combination of education and experience may be accepted.

Responsibilities

  • Oversee QA programs supporting customer accounts and audits.
  • Ensure adherence to regulatory standards.
  • Lead compliance initiatives and manage staff.

Skills

Knowledge of GXP regulations
Leadership skills
Communication skills
Problem-solving skills
Risk analysis skills

Education

Bachelor's Degree in life sciences or pharmaceutical sciences

Tools

Word-processing applications
Spreadsheets
Database applications
Job description

We are seekinga Quality Assurance Manager to join IQVIA Laboratories in Durham, NC.

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

As a Quality Assurance Manager, you will oversee and coordinate QA programs supporting customer accounts, audits, and quality systems at a regional and global level. You will lead compliance initiatives, manage staff, and ensure adherence to regulatory standards.

What you’ll be doing:
  • Provide guidance and training on GXP regulations, corporate standards, and quality policies

  • Oversee documentation, reporting, and resolution of compliance issues

  • Lead training initiatives across departments on quality services and regulatory updates

  • Ensure timely follow-up and resolution of audit findings

  • Evaluate SOPs and procedures for regulatory compliance and process improvement

  • Author and maintain Quality Assurance SOPs

  • Manage audit scheduling, reporting, and database accuracy

  • Supervise QA staff, including performance reviews, development planning, and HR actions

What We Are Looking For:
  • Bachelor’s Degree preferred in life sciences, pharmaceutical sciences, or related field

  • Minimum 7 years of QA experience in pharmaceutical, technical, or related area, including GCP QA

  • Minimum 5 years of management experience

  • Other Equivalent combination of education, training, and experience may be accepted in lieu of degree

The Knowledge, Skills and Abilities needed for this role:
  • Strong knowledge of GXP regulations, pharmaceutical R&D processes, and QA systems

  • Proficiency in word-processing, spreadsheets, and database applications

  • Excellent leadership, communication, problem-solving, and risk analysis skills

What We Offer You:

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs.We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

To learn more about our benefits, visithttps://jobs.iqvia.com/benefits.

If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

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

The potential base pay range for this role, when annualized, is $0.00 - $0.00. 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

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