ASSOCIATE DIRECTOR, QUALITY ASSURANCE
$109.86k - $191.06kDuke University
Associate Director, Quality AssuranceWork Arrangement: On-SiteLocation: Durham, NC, US, 27710School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.Be You. The Office of Regulatory Affairs and Quality (ORAQ) at Duke University is seeking an Associate Director, Quality Assurance to provide strategic leadership for GMP quality programs supporting the development and manufacture of innovative therapies, biologics, vaccines, medical devices, and other regulated products. In this highly visible role, you will serve as a key quality leader, partnering with Duke investigators, GMP facility leadership, regulatory stakeholders, and external sponsors to ensure quality systems effectively support clinical and manufacturing programs. You will help shape and oversee quality management systems across multiple GMP facilities and product platforms, provide expert guidance on regulatory requirements, support inspections and audits, and lead initiatives that advance Duke's mission of translating scientific discoveries into therapies that improve human health. This position reports to the Director, Quality and plays a critical role in supporting compliance, operational excellence, and continuous improvement across Duke's GMP programs.Minimum Requirements: Bachelor's degree in a scientific discipline (Bachelor of Science or Bachelor of Arts). Minimum of five years of experience in a GxP-regulated environment. Experience leading complex projects and multidisciplinary teams with measurable outcomes. Experience making independent Quality Assurance decisions and providing strategic quality guidance. Experience representing Quality Assurance during audits, inspections, and senior leadership meetings. Experience evaluating and improving quality systems, including conducting gap assessments and monitoring effectiveness. Expert knowledge of GxP regulations and quality systems. Demonstrated ability to communicate effectively and influence stakeholders at all organizational levels. Proven ability to manage multiple priorities and lead cross-functional initiatives.Preferred Qualifications: Master's degree or PhD in a related scientific field. Experience supporting diverse product development programs, including drugs, biologics, cellular therapies, vaccines, medical devices, blood products, and HCT/Ps. Experience developing and delivering regulatory or quality training programs. Strong organizational, problem-solving, and relationship-management skills. Ability to build, mentor, and retain high-performing teams. Excellent verbal, written, and interpersonal communication skills.Other Requirements: Ability to interpret and apply U.S. and global GMP regulations and regulatory guidance. Ability to effectively represent Duke with regulatory agencies, external sponsors, vendors, and other stakeholders. Participation in internal and external audits, inspections, and regulatory interactions as needed.Be Bold. As the Associate Director, Quality Assurance, you will: Lead and oversee GMP quality management systems across multiple facilities, product platforms, and development programs to ensure compliance and operational effectiveness. Provide strategic quality leadership for GMP initiatives, partnering with ORAQ leadership, investigators, manufacturing teams, and external sponsors to address quality, compliance, and risk management considerations. Guide complex quality activities including deviations, investigations, out-of-specification results, product release decisions, CAPAs, and continuous improvement efforts. Represent Quality Assurance during audits, regulatory inspections, sponsor interactions, and cross-functional project teams while serving as a trusted subject matter expert. Develop and mentor staff by leading quality professionals, fostering professional growth, and supporting a culture of quality throughout Duke's GMP operations.Choose Duke. Duke University is a world-renowned academic and research institution committed to advancing scientific discovery and improving human health. ORAQ supports innovative clinical and manufacturing programs that bring cutting-edge therapies from concept to patient impact while maintaining the highest standards of quality and regulatory compliance. As part of our team, you will collaborate with leading researchers, clinicians, regulatory professionals, and manufacturing experts while helping shape quality systems that support groundbreaking therapies and research initiatives. This is an opportunity to make a meaningful impact on programs that advance science and improve lives.Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $109,856.00 to USD $191,062.00. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer. Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members.Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy- related conditions), sexual orientation, or military status. Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas—an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.Essential Physical Job Functions: Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: View email address on click.appcast.io; phone: View phone number on click.appcast.io).
$88.6k - $246.6k
Job OverviewProvide 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...SuggestedFull timePart timeWork at officeImmediate startWorldwide$88.6k - $246.6k
...accounts, functional accounts, audit and inspection program, or QA quality management system at a regional and/or global level. Provide... .../efficiency improvement initiatives. Manage the quality assurance oversight of projects, assignments, training and staff. Essential...SuggestedFull timePart timeImmediate startWorldwide$138.6k - $257.4k
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$138.6k - $257.4k
Job Description SummaryLocation: Morrisville, NCJoin Novartis as our QA Compliance and Systems Head and help shape the quality foundation that enables the delivery of medicines to patients worldwide. This is a unique opportunity to join our new Small Molecule manufacturing...Full timeWorldwide- ...position as one of the country's leading integrated service providers. Job Summary EMCOR Government Services (EGS) is seeking a Quality Control Manager (QCM) to provide Facilities Operations Maintenance and support Services to a Government Agency in Research...Full timeContract workFor contractorsWork at office
$147k - $213k
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Job DescriptionAssociate Director - Global Engineering SolutionsOur Engineers support internal... ...Medicines. The GES group is seeking an Associate Director of Engineering to manage large... ...GES, Site Engineering, Operations, Quality, EHS, Maintenance, Technology, Procurement...Full timeContract workFor contractorsLocal areaFlexible hours- ...as well as sustaining the product post launch). The Program Manager/Core Team Leader is ultimately responsible for the execution, quality and results of his or her project and the success of the resulting product in the market along with ensuring the core products within...Full timeInterim roleWork at officeRemote workWorldwideFlexible hours
$100k - $145k
...hybrid, and standalone energy storage projects. As we add to our team, we are seeking candidates at either the Senior Manager or Associate Director level, depending on their experience and qualifications.This role will be responsible for advising developers and project...Work at officeLocal areaRemote work3 days per week$140k - $193k
...platform for the LGBTQ+ business community. Please do not contact the recruiter directly. About this Role At Biogen, the Associate Director, Site Training is responsible for leading the strategy, execution, and continuous improvement of training programs supporting...Temporary workLocal area$146k - $194k
...companies. For more information, please visit grail.com The Associate Director, Operational Excellence is central to driving continuous improvement... ...data into actionable insights, enabling scalable, high‑quality execution in a regulated environment. This role works on‑...Full timeWork at officeLocal areaFlexible hours$75k - $95k
...The fastest-growing philanthropic advisory firm in the nation, Arabella is also a certified B Corporation. ABOUT THE POSITION Associate Directors are experienced operations professionals with strong project management skills who oversee a portfolio of fiscally sponsored...Relocation package- ...Director, Thought Leader Engagement & Peer-to-Peer Marketing - Hematology Field-Based / Remote Position Overview GSK Oncology... ...scalable faculty development frameworks to strengthen educational quality and customer impact. Ensure coordinated management of...Temporary workWork at officeLocal areaRemote workHome office
- ...AskBio seeks an Associate Director; Translational Medicine Project Lead to guide preclinical safety/pharmacology strategies across CNS, Muscle Metabolism, Ophthalmology, and Renal programs. Based in Morrisville, NC, you will represent Translational Medicine on program...
- ...Position Summary The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the... ...process development, analytical development, manufacturing, quality, and program leadership to ensure that CMC development plans...Contract work
- ...company specializing in severe orphan diseases to recruit an Associate Director, Medical Affairs - Southeast. This role will serve as a key... ...the Medical Officer Report pharmacovigilance (PV), product quality (PQ), or medical information (MI) requests within 24 hours,...Flexible hours
- The Quality Control Manager (QCM) is responsible for developing, implementing, and maintaining the contractor's Quality Control Program... ...Manager to preserve objectivity and authority in quality assurance oversight across all EPA-RTP facilities. Responsibilities Develop...Contract workFor contractors
- ...help build a trusted vendor data ecosystem? As a Sr. Vendor Data Quality Analyst at Fidelity Investments, you will play a key role in... ...laws and regulations may restrict Fidelity from hiring and/or associating with individuals with certain Criminal Histories....Full time
$110k - $140k
...A leading research organization is seeking a Mid-Senior Quality Assurance Manager to support the development of new drugs through expert analysis of biological specimens. This role entails managing audits, authoring SOPs, and ensuring compliance with quality management...- ...Make clear commitments and follow through.Position Summary The Associate Director, Process Development is a key position in the Cell Line &... ...technologies for increased productivity, recovery, product quality and/or improved cost of goodsCollaborate cross-functionally...Full timeWork at officeLocal area
$129k - $203.1k
...manufacturing plants with a “Safety First, Quality Always, Inclusion for All” mindset... ...Description:We are seeking an Associate Director, Operations for a capital project start... ...with sterile processing and sterility assurance practices and guidelinesRequired Skills...Full timeFor contractorsLocal area$110k - $140k
...should have a strong background performing audits and managing quality issues within a regulated laboratory environment. Minimum Requirements... ...(QMS) documents (e.g., SOPs, templates, manuals and policies) assuring compliance with the applicable regulations (e.g., GLPs, Part 11...Full timeContract work- ...work with CDMOs and external labs About the Position The Associate Director, Analytical Sciences will provide scientific leadership and... ..., Formulation Development, Pilot Plant, Bioassay, Quality, Manufacturing, and Regulatory Affairs to ensure integrated...Full timeWorldwide
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