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Director Quality Management Jobs in Delaware (NOW HIRING)

Chemour

Business Quality Leader

Wilmington, DE · On-site

$141 - $221/hr

Previous experience in a Quality Manager, Senior Quality Manager, Business Quality, Global Quality, or Quality Director-level role.Experience supporting multiple manufacturing sites, complex product ...

None

Business Quality Leader

Wilmington, DE · On-site

$141 - $221/hr

Previous experience in a Quality Manager, Senior Quality Manager, Business Quality, Global Quality, or Quality Director-level role. * Experience supporting multiple manufacturing sites, complex ...

Merck & Co.

Director Operations for Drug ProductDo you aspire to secure a critical role in the production of ... Upholding our Manufacturing Division Quality Management System (QMS) requirements, you will manage ...

Merck & Co., Inc.

Director, Operations

Wilmington, DE · On-site

Director Operations for Drug Product Do you aspire to secure a critical role in the production of ... Upholding our Manufacturing Division Quality Management System (QMS) requirements, you will manage ...

MSD Malaysia

Director, Operations

Wilmington, DE · On-site

$173 - $273/hr

Director Operations for Drug Product do you aspire to secure a critical role in the production of ... Upholding our Manufacturing Division Quality Management System (QMS) requirements, you will manage ...

New

MSD

Director, Operations

Wilmington, DE

Director Operations for Drug Product Do you aspire to secure a critical role in the production of ... Upholding our Manufacturing Division Quality Management System (QMS) requirements, you will manage ...

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Director Quality Management information

See Delaware salary details

$31K

$125.7K

$213.7K

How much do director quality management jobs pay per year?

As of Aug 29, 2026, the average yearly pay for director quality management in Delaware is $125,709.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,100.00 and $151,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a director of quality management?

To thrive as a Director of Quality Management, you need in-depth knowledge of quality assurance principles, regulatory compliance, process improvement methodologies, and typically a degree in a related field such as healthcare, engineering, or business. Familiarity with quality management systems (e.g., ISO 9001), data analytics tools, and relevant certifications like Certified Professional in Healthcare Quality (CPHQ) are often required. Exceptional leadership, communication, and problem-solving abilities enable effective collaboration across departments and drive organizational change. These skills ensure the organization consistently meets quality standards, improves outcomes, and mitigates risk.

How does a director of quality management typically collaborate with cross-functional teams to drive quality initiatives?

A Director of Quality Management works closely with teams across the organization, including operations, product development, regulatory affairs, and customer service, to implement and uphold quality standards. This role often leads cross-functional meetings, facilitates root cause analyses, and coordinates the rollout of process improvements. Effective communication and the ability to build consensus are crucial, as the Director must align diverse departments around shared quality goals. By fostering collaboration, the Director ensures that quality initiatives are integrated seamlessly into daily operations and long-term strategies.

What is the difference between Director Quality Management vs Quality Assurance Manager?

AspectDirector Quality ManagementQuality Assurance Manager
ResponsibilitiesOversees entire quality management systems, develops policies, and ensures compliance across departments.Implements quality assurance processes, monitors product quality, and manages QA teams.
CertificationsISO 9001 Lead Auditor, Six Sigma, CQEISO 9001 Lead Auditor, Six Sigma, CQE
Work EnvironmentStrategic, cross-departmental, executive-levelOperational, team-focused, project-based
Industry UsageCommon in manufacturing, healthcare, and large organizationsPrevalent in manufacturing, software, and service industries

While both roles focus on quality, the Director of Quality Management has a broader, strategic oversight role, whereas the Quality Assurance Manager concentrates on implementing and managing specific QA processes within teams.

What does a director of quality management do?

A director of quality management oversees an organization’s quality assurance and control processes to ensure products or services meet industry standards and customer expectations. They develop quality policies, lead audits, analyze data for continuous improvement, and coordinate with departments to implement quality initiatives, often requiring knowledge of quality management systems like ISO and leadership skills. The role typically involves strategic planning, team management, and ensuring compliance with regulatory requirements.

What are the most commonly searched types of Quality Management jobs in Delaware?

The most popular types of Quality Management jobs in Delaware are:

Director Quality Management jobs near you
Infographic showing various Director Quality Management job openings in Delaware as of June 2026, with employment types broken down into 1% As Needed, 95% Full Time, 3% Part Time, and 1% Temporary. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $125,709 per year, or $60.4 per hour.

Director Quality Management Late Development Oncology Clinical Operations (Americas)

AstraZeneca

Wilmington, DE • On-site

Full-time

Posted 13 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

Responsible for the analysis of company quality requirements and the establishment, implementation and control of quality assurance systems and procedures across multiple disciplines. Has extensive experience across a range of business areas. Will lead a team of quality professionals. Reports to the Senior Director, Quality Management.
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you are our kind of person. At the heart of AstraZeneca, our team is committed and encouraged to follow the science. Driven by our curiosity, passion, and determination, we are paving the way to change the practice of medicine in Oncology.
The Oncology Clinical Quality Director (O-CQD) will be responsible for the management and oversight of the LDO Quality Associate Directors.
Typical Accountabilities
  • Build strong relationships and strategic partnerships; collaborate proactively across functions and HUBs to drive adherence to compliance requirements while operating effectively in ambiguity.

  • Lead, develop, and coach a geographically and culturally diverse team of quality professionals.

  • Embed quality frameworks, risk management approaches, and compliance strategy with senior leadership and employees.

  • Interpret complex data to assess quality performance and recommend compliance improvements and risk mitigations across LDO Clinical Operations.

  • Provide expert quality advice and coaching to direct reports and LDO ClinOps teams on complex compliance matters, including risk identification and compliance improvement strategies, initiatives, and plans.

  • Support LDO ClinOps teams in driving a quality mindset and culture, including resolution of sophisticated quality matters (e.g., serious breaches, fraud, poor quality).

  • Lead Quality Management Reviews by consolidating and strategically communicating key compliance-relevant insights on country/regional and functional performance to enable continuous improvement.

  • Seek, engage, and lead compliance collaborations across LDO ClinOps, and other R&D Functions to deliver effective, sustainable issue resolution.

  • Identify and consolidate LDO clinops/country/regional and HUB risks; escalate as required; define, support, and lead (as appropriate) risk mitigation (compliance) activities end-to-end.

  • Advise on AZ procedural framework (global clinical processes, procedural documents, Quality & Compliance manual) and applicable guidelines/standards and local regulations (including ICH-GCP).

  • Provide senior-level advice on local and/or international clinical trial regulations; remain current on changes and ensure teams/processes are updated accordingly.

  • Share learnings from audits and inspections with LDO clinops employees; cascade global /regional learnings across local, regional, and global stakeholders.

  • Act as the interface with global stakeholders (e.g., legal advice, ethics, nominated signatory, GxP function) for quality-related topics.

  • Represent the function in external expert groups (regulatory or operational) as required.

Minimum Requirements
  • Bachelor's or advanced degree required in a science related field.

  • Approximately 10 years demonstrating excellent knowledge of international regulations and guidelines; deep experience engaging global regulators (FDA, PMDA, EMEA, Health Canada), including inspection conduct in the clinical research industry.

  • Significant clinical research quality and compliance experience; deep knowledge of ICH-GCP and applicability to clinical operations at both sponsor and site levels.

  • Strong understanding of the drug development process and related GxP activities, including successful clinical study delivery (e.g., ICH-GCP, study management).

  • Broad experience in the pharmaceutical industry within a GxP-regulated environment.

  • Proven leadership and line management skills that helps teams excel in a regulated environment.

  • Excellent communication skills with a proven track record of effective cross-functional and global networking.

  • Strong critical thinking and risk-based decision-making skills.

  • Effective analytical, problem-solving, negotiation, and conflict resolution skills.

  • Demonstrated ability to set and manage priorities, performance targets, and project initiatives in a global environment.

  • Ability to collaborate proactively, operate effectively in ambiguity, and build strong customer relationships/strategic partnerships to enable process and system harmonization/standardization.

Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
So, what's next?
Are you already imagining yourself joining our team? Good, because we can't wait to hear from you!
Date Posted
17-Aug-2026
Closing Date
07-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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