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Director Quality Systems Jobs in Delaware (NOW HIRING)

Vicdania Home Health

Clinical Director

Dover, DE · On-site

$120 - $160/hr

... systems. The Clinical Director directs and supervises professional and auxiliary personnel ... Coordinate with continuous Quality Improvement Committee the timely implementation of corrective ...

Vicdania Home Health

Clinical Director

Dover, DE · On-site

$80K - $108K/yr

... systems. The Clinical Director directs and supervises professional and auxiliary personnel ... Coordinate with continuous Quality Improvement Committee the timely implementation of corrective ...

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 ...

MSD

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 ...

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 ...

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.

Associate Director, Maintenance - Wilmington Biologics SitePosition SummaryThe Associate Director ... Partner with Quality, Validation, Metrology, and system owners to coordinate post-maintenance ...

Chick-fil-A

Director

Newark, DE · On-site

Are committed to delivering excellent service and quality. * Are adaptable and open to focusing on ... annual system-wide sales. Today, Chick-fil-A is America's #1 fast food restaurant. Working at a ...

Chick-fil-A

Director

Newark, DE · On-site

Are committed to delivering excellent service and quality. * Are adaptable and open to focusing on ... annual system-wide sales. Today, Chick-fil-A is America's #1 fast food restaurant. Working at a ...

Chick-fil-A

Director

Newark, DE · On-site

Are committed to delivering excellent service and quality. * Are adaptable and open to focusing on ... system-wide sales. Today, Chick-fil-A is America's #1 fast food restaurant. Work schedule * 8 hour ...

Boys-

Club Director

Dover, DE · On-site

$65 - $90/hr

Take specific steps to ensure quality improvement, such as the Club's active participation in each ... Ensure Club adherence to administrative and operational systems in support of organization policies ...

New

Stellantis

Design Quality Lead BCIM

Newark, DE

Prepare and deliver bi‑weekly project reviews with the Director. * Develop and present materials ... Provide 1:1 AUROS/PLM training for DREs to ensure proper system usage and documentation quality.

Stellantis

Design Quality Lead BCIM

Milford, DE

Prepare and deliver bi‑weekly project reviews with the Director. * Develop and present materials ... Provide 1:1 AUROS/PLM training for DREs to ensure proper system usage and documentation quality.

Stellantis

Design Quality Lead BCIM

Smyrna, DE · On-site

Prepare and deliver bi‑weekly project reviews with the Director. * Develop and present materials ... Provide 1:1 AUROS/PLM training for DREs to ensure proper system usage and documentation quality.

Stellantis

Design Quality Lead BCIM

Middletown, DE

Prepare and deliver bi‑weekly project reviews with the Director. * Develop and present materials ... Provide 1:1 AUROS/PLM training for DREs to ensure proper system usage and documentation quality.

Stellantis

Design Quality Lead BCIM

Dover, DE

Prepare and deliver bi‑weekly project reviews with the Director. * Develop and present materials ... Provide 1:1 AUROS/PLM training for DREs to ensure proper system usage and documentation quality.

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Director Quality Systems information

What is a director quality systems?

A Director of Quality Systems is a senior management professional responsible for overseeing the development, implementation, and maintenance of an organization's quality management systems. They ensure that products and processes comply with industry standards, regulatory requirements, and company policies. This role often involves leading teams, developing quality strategies, conducting audits, and driving continuous improvement initiatives across the organization. Directors of Quality Systems play a critical part in safeguarding product quality, customer satisfaction, and regulatory compliance.

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

To thrive as a Director of Quality Systems, you need deep expertise in quality management principles, regulatory compliance, process improvement, and typically a relevant degree such as in engineering or life sciences. Familiarity with quality management systems (QMS) like ISO 9001, FDA regulations, and proficiency with tools such as CAPA, risk management software, and internal audit systems is essential. Strong leadership, strategic thinking, and effective communication distinguish top performers in this role. These skills ensure the organization maintains high quality standards, meets regulatory requirements, and drives continuous improvement across all operations.

What are some common challenges faced by a director quality systems when implementing new compliance standards across an organization?

A Director of Quality Systems often encounters challenges such as resistance to change from staff, alignment of existing processes with new regulatory requirements, and ensuring consistent training across departments. Effective communication and cross-functional collaboration are key to overcoming these hurdles. The role typically involves working closely with leadership, operations, and regulatory teams to ensure that new standards are understood and integrated smoothly, minimizing disruptions while maintaining compliance.

What is the difference between Director Quality Systems vs Quality Manager?

AspectDirector Quality SystemsQuality Manager
ResponsibilitiesOversees quality systems, compliance, and strategic quality initiatives across departmentsManages daily quality operations, audits, and team supervision
CertificationsISO 9001 Lead Auditor, CQE, Six SigmaISO 9001 Lead Auditor, CQE, Six Sigma
Work EnvironmentStrategic planning, cross-departmental collaborationOperational focus, team management
Industry UsageCommon in regulated industries like pharmaceuticals, medical devicesWidely used in manufacturing, production facilities

The main difference between a Director Quality Systems and a Quality Manager lies in scope and strategic focus. The Director typically oversees the entire quality system, ensuring compliance and strategic alignment, while the Quality Manager handles daily quality operations and team supervision. Both roles often require similar certifications and work in regulated industries, but the Director's role is more strategic and cross-departmental.

What job categories do people searching Director Quality Systems jobs in Delaware look for?

The top searched job categories for Director Quality Systems jobs in Delaware are:

What cities in Delaware are hiring for Director Quality Systems jobs?

Cities in Delaware with the most Director Quality Systems job openings:

Director Quality Systems jobs near you
Infographic showing various Director Quality Systems job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Chemical Process Engineers / Senior Chemical Process Engineer

Wilmington PharmaTech Company LLC

Newark, DE

Full-time

Re-posted 24 days ago

Job description

Wilmington PharmaTech (WPT) is looking for a Process / Production Engineer with cGMP experience in the pharmaceutical industry to work in the Newark, DE area. The nature of this position is supporting the manufacturing team that creates drug products by working closely with supervisors, GMP operators, maintenance technicians and QA colleagues. Ideal candidates should have a strong understanding of Good Manufacturing Practices (GMP) and new product development projects, and pharmaceutical/ chemical manufacturing. The position is set in a fast-paced start-up environment and shall require the individual to work on a broad range of tasks. A qualified applicant should have the skills or previous knowledge of the below tasks:

  • Configure plant equipment, such as reactors, pumps and filters for process scale-up from laboratory development work and assist in preparation of batch records.
  • Understand and help to develop pre-production equipment readiness checklists.
  • Works closely with QA to ensure proper and documented cleaning of equipment before and after production campaigns and between batches as needed.
  • Participates in the initial set up and operation of the equipment in a cGMP setting.
  • Able to define and carry-out equipment training programs.
  • Create, read and understand batch records, SOP’s and related documents
  • Comply with all cGMP requirements as directed by the Quality department and management.
  • Maintain thorough, accurate, and legible documentation required fulfilling the cGMP requirement for the plant.
  • Be accountable for all documentation and production, which is his/her responsibility.
  • Have a basic understanding of materials handling to prevent contamination and to comply with cGMP’s and customer requirements.
  • Follow all safety procedures at all times and report any potential safety hazards to on-site safety staff or to team leader.
  • Experience with potent compounds (HPAPI) is a plus.
  • Must be able to demonstrate in-depth understanding of technical equipment, Quality Systems and the interface between equipment and the associated automation.
  • Understanding of facility technology, system troubleshooting using root cause analysis tools, CAPA’s and change controls highly preferred.
  • Other duties as assigned.

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