Director of Quality

Quality Engineering Director

Location: Stuttgart, Arkansas,

Are you an experienced quality engineering leader with a background in metal fabrication, machining, and assembly? Join our team and take charge of quality operations in a 750,000 sq. ft. manufacturing facility employing 1,700 dedicated non-union workers.

Key Responsibilities:

• Quality Engineering Strategy:
• Develop, execute, and maintain processes and systems to ensure all products meet customer and corporate specifications.
• Lead the design and implementation of a comprehensive Quality Management System (QMS).
• Continuous Improvement:
• Identify, validate, and lead manufacturing process improvements that enhance product quality and process yields.
...

The Senior Manager/Director of Quality Assurance will be a key leader within the nutpods Quality Assurance team, acting as the primary representative of the company in all quality-related matters with suppliers, co-manufacturers, and distribution partners. This role demands a strong commitment to maintaining nutpods’ rigorous standards for food safety, product quality, and regulatory compliance across the entire supply chain. The successful candidate will play a vital role in fostering and sustaining strong relationships with stakeholders, ensuring that nutpods’ quality expectations and values are consistently upheld. Key responsibilities include:

JOB RESPONSIBILITIES:

• Lead Quality Assurance Team, mentoring QA Regulatory Specialists to foster high performance and ensure quality and regulatory compliance.
• Develop and enhance quality programs, continuously improving existing initiatives to meet evolving business and regulatory...

As the holiday season approaches, we want to inform you that response times and the hiring process may be slightly extended due to business team schedules. We truly appreciate your patience and understanding during this period and remain committed to keeping you informed as we review applications. Thank you for considering a role at ŌURA—we look forward to learning more about you!

Our mission at Oura is to empower every person to own their inner potential. Our award-winning products help our global community gain a deeper knowledge of their readiness, activity, and sleep quality by using their Oura Ring and its connected app. We've helped over 2.5 million people understand and improve their health by providing daily insights and practical steps to inspire healthy lifestyles.

Empowering the world starts with living our values and empowering our team. As a quickly growing company focused on helping people live healthier and happier...

We are seeking an experienced Quality Engineering Leader to oversee and drive the quality engineering strategy in a large-scale, 750,000-square-foot metal fabrication and machining facility with a team of 1,700 non-union employees. This role is critical in ensuring that all products manufactured at the facility consistently meet both customer and corporate standards for quality.

Key Responsibilities:

• Develop, execute, and maintain robust processes and systems to ensure product quality meets all required specifications.
• Lead the design and implementation of an effective Quality Management System (QMS) tailored to the facility’s unique production needs.
• Drive continuous improvement initiatives focused on enhancing product quality, process yields, and overall manufacturing efficiency.
• Identify, validate, and lead projects aimed at improving manufacturing processes and achieving higher standards of quality and...

This Full-Time Director of Quality Management position is located at our ContinueCARE Hospital at Hendrick Medical Center in Abilene, TX. ContinueCARE Hospital at Hendrick Medical Center is a 23-bed long term acute care hospital (LTACH) located on the seventh floor of the Jones Building at Hendrick Medical Center. A typical LTACH patient may require care for: ventilator weaning, complex wounds, infections requiring IV antibiotics, complications from extensive surgery, multi-system failures, TPN, neurological / traumatic injuries, and those not yet able to participate in acute rehabilitation due to medical complexity.

The Director of Quality Management develops, implements and maintains an effective, ongoing, organization wide, data driven Quality Assessment Performance Improvement (QAPI) Program. Establishes a planned systematic and interdisciplinary approach to improving care treatment and services with hospital leaders. Creates a culture that shifts primary...

MEMX  is searching for a  Director, Quality Assurance to oversee the software testing of MEMX’s software products. A successful candidate will lead MEMX’s Software QA process, manage MEMX’s test engineering team, coordinate changes with our development team, and demonstrate the ability to fully automate the testing process.   The ideal candidate has hands on testing experience at a financial institution, preferably a stock exchange.   

MEMX currently has a U.S. presence in these states: California, Connecticut, Delaware, Florida, Georgia, Illinois, Kansas, Maine, Maryland, Michigan, Nevada, New Jersey, New York, North Carolina, Oregon, Pennsylvania, & South Carolina. 

*If you live outside of the above states, please list in your application and our team will evaluate. 

What You’ll Do 

• Manage MEMX’s QA team; 
...

SAGA Diagnostics is a personalized cancer diagnostics and disease monitoring company focused on molecular genetic analysis of circulating tumor DNA (ctDNA). The company’s mission is to improve precision cancer medicine, provide more accurate treatment monitoring, and improve patient survival using minimally-invasive liquid biopsy cancer testing services. SAGA’s proprietary tests can help patients, oncologists, and drug developers detect actionable mutations, stratify patient groups, and monitor treatment response, residual disease, and disease recurrence at unprecedented sensitivity and scale. 

SAGA Diagnostics recently established a US operation in Research Triangle Park (RTP) and is looking for a talented and highly motivated Director of Quality Assurance with a strong interest in advancing our mission to revolutionize cancer diagnostics through the use of liquid biopsies. The Director of Quality Assurance will ensure compliance with CAP/CLIA, NYS, GCP/GCLP, and other...

Acentra is looking for a Software Quality Assurance Director to join our growing team.

Job Summary:

As the Software Quality Assurance Director at Acentra Health, you will be a key leader within our organization, playing an integral role in driving innovation and excellence in software quality. In this high-impact position, you will lead best practices to achieve a zero-defect production environment, fostering continuous improvement and ensuring we meet or exceed business objectives. Your leadership will directly contribute to the success of our nationwide quality program, making a tangible impact on our mission to deliver top-tier healthcare solutions.

Join us and take the lead in shaping the future of software quality at Acentra Health—where your expertise will drive meaningful outcomes that support healthcare excellence.

Job Responsibilities:

• Lead the Software Quality...

About Us

We are only accepting applications through verified recruitment websites listing our job postings (i.e. LinkedIn, Workable, Indeed, etc). Dymax will only contact potential candidates from email addresses in @dymax.com.

Dymax, part of the Bachmann Chemical & Engineering family of brands is based out of Torrington, Connecticut. Dymax is globally recognized as a pioneer in the development of light-curable adhesives and curing equipment. Today, our expansive portfolio of innovative adhesives, coatings, and maskants are supported by dispense solutions and cutting-edge UV and LED light-curing equipment. Unlike our competitors who supplying standard products, Dymax focuses on the customer experience by tailoring solutions that help customers lower costs, reduce their carbon footprint, improve efficiency, and drive profitability. Our focus on being a customer intimate organization has led us to where we are today: a rapidly...

Tasty Brands/TRACCO is a well-established, fast growing national company that is focused on providing great tasting, nutritious food for K12 school foodservice customers and private brands of selected retailers. With a focus on collaboration, best practices, and continuous improvement, we are looking for people who want to join us for a long career and be part of a great success story. Our most successful people are self-starters, work well in collaboration with others, see the big picture and like to win.

We have an outstanding team of motivated professionals who work well together in a fun and team spirit type atmosphere. Our mission is driven by our core values – urgency, accountability, proactivity, teamwork, and integrity. We are looking for the next “great fit” to join our growing team!

Overview

The Director of Quality Assurance will be responsible for managing the plant's...

RP Professional Services, LLC (RP) is a rapidly growing government consulting firm headquartered in Ashburn, Virginia. We’re an 8(a), Service-Disabled Veteran-Owned Small Business (SDVOSB) that exclusively enables the missions of U.S. Federal agencies through superior mission support and technology integration. Our dedication to our employees and clients is driven by our promise to deliver Excellence, Value, and Flexibility. "People, not just Resources" is more than our motto; it's the foundation on which we are built! At RP, we take pride in who we are and what we deliver. 

Job Summary: We are seeking a dynamic and highly qualified Subject Matter Expert & Senior Quality Assurance Analyst to support our health and social services recovery initiatives. The ideal candidate will possess a Master’s degree and a minimum of 10 years of relevant experience, or equivalent expertise. This dual-role position requires a unique blend of specialized knowledge and...

CSBio is a peptide contract manufacturing founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. In 2004, we opened our peptide production facility in Menlo Park, CA and in 2014, we expanded our production capability through the addition of a new, state of the art building dedicated to cGMP peptide production. In 2017, we passed a FDA inspection and were recommended to be approved for commercial drug substance manufacturing. In 2023, we added additional cGMP clinical production capacity in Milpitas, CA.

Job Duties:

• Host and provide responses to client audits and regulatory inspections.
• Oversee Quality Management System at CSBio encompassing quality investigations including...

***MUST HAVE MANAGED CARE EXPERIENCE WITHIN NYS HEALTHCARE PROVIDER NETWORKS***

The Director of Claims Quality has responsibility for the creation, delivery, and ongoing facilitation of a data and metrics-driven Claims Quality Assurance and Performance oversight program, which includes defining frameworks/benchmarks, calibration, and reporting of a program towards set benchmarks while promoting a continuous improvement culture.

Furthermore, the Director of Claims Quality is responsible for the management/oversight of claims quality, claims compliance, training and remediation, user acceptance testing (UAT), claims adjustments, and correspondence/inquiries/reconsiderations/appeals. This includes overseeing staffing, implementing, and maintaining policies, procedures, and workflows across the Claims department that is compliant with all applicable Local, State, and Federal Regulations. Also, this position is responsible for developing and enhancing...

Who is CorDx？  
 

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.  

Position: QA Director
Location: Alpharetta/Chamblee
Position Type: 5 days Onsite Exempt Position

Job Summary: We are seeking an experienced Quality Assurance Director to lead our quality assurance team in the development, manufacturing, and distribution of Class II IVD devices. The ideal candidate...

Job Title: Executive Director, Quality & Compliance

Department: Quality & Compliance

Reporting To: President, Drug Manufacturing US

Classification: Exempt

Salary Range: 200k-240k/yr, Depending on Experience

What We Do

BioDuro-Sundia is one of the premier Contract Research, Development and Manufacturing Organizations (CRDMO) globally, with more than 2,200 employees.  Our US operations are US headquartered in Irvine, CA. Our 7 global facilities provide integrated solutions and exceptional services to our clientele for challenging preclinical and clinical trial projects. With capabilities spanning Drug Discovery, Development, and Manufacturing, it is no surprise that BioDuro-Sundia is a leading partner of choice.

Why BioDuro-Sundia?

Take the next step in your career and join...

Be more than just an employee number! Join Terran Orbital, a leader in innovation, manufacturing, and operations in the satellite industry. We are a pioneer in the miniaturization of space technologies and the delivery of responsive space solutions. We are a unique, fast-growing, and trusted team focused on quickly and economically designing, building, launching, and operating state-of-the-art satellites for advanced mission constellations.

Terran Orbital is seeking an experienced Director, Quality to join our growing team. Reporting to the VP of Safety& Mission Assurance, the Director of Quality will be responsible for building and leading a team of Quality professionals. Effective collaboration with procurement, manufacturing engineering, design engineering, and program teams is critical to the role. 

Key Duties and Responsibilities

• Responsible for...

We are currently seeking a highly skilled and experienced Director/Senior Director of Quality Control for Cell Therapy to join our client's growing team. In this role, you will be responsible for overseeing all quality control activities related to cell therapy Quality Control processes.

Key Responsibilities:

• Develop and implement quality control strategies and programs to ensure compliance with relevant regulations and industry standards.
• Manage a team of QC professionals, providing guidance and support in their daily activities.
• Oversee the testing and release of raw materials, intermediates, and final cell therapy products.
• Ensure timely and accurate completion of QC testing and documentation, including assay development, qualification, and validation.
• Collaborate with cross-functional teams to establish and maintain robust quality systems and processes.
• Participate in the development and review of protocols, SOPs,...

CNSI and Kepro are now Acentra Health! Acentra Health exists to empower better health outcomes through technology, services, and clinical expertise. Our mission is to innovate health solutions that deliver maximum value and impact.

Lead the Way is our rallying cry at Acentra Health. Think of it as an open invitation to embrace the company’s mission, actively engage in problem-solving, and take ownership of your work daily. Acentra Health offers you unparalleled opportunities. In fact, you have all you need to take charge of your career and accelerate better outcomes – making this a great time to join our team of passionate individuals dedicated to being a vital partner for health solutions in the public sector.

Acentra seeks a Software Quality Assurance Director to join our growing team.

Job Summary:

The Software Quality Assurance Director plays a critical role in ensuring the highest...

Role: Director, Quality Assurance - Full-time Employee

Location: Charleston, South Carolina, USA

As the PTW Director of Quality Assurance, you will lead and manage the global development QA organization. This includes overseeing a large global team, workforce planning, staffing, and processes, while supporting other leadership directors. Your responsibilities will encompass all aspects of QA, including feature development, AI-QA Automation, testing capabilities, and compliance.

You will collaborate closely with our clients’ Game Development and Publishing teams to address everyday challenges and streamline deliveries. By partnering with our clients’ development disciplines, you will proactively innovate and enhance our QA philosophies and best practices. You will manage and mentor Quality Assurance professionals, fostering the growth of QA leadership to cultivate new leaders. As the QA Director, you will ensure global alignment within the...

Who is CorDx？  
 

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.  

Position: QA Director
Location: Alpharetta/Chamblee
Position Type: 5 days Onsite Exempt Position

Job Summary: We are seeking an experienced Quality Assurance Director to lead our quality assurance team in the development, manufacturing, and distribution of Class II IVD devices. The ideal candidate...

CNSI and Kepro are now Acentra Health!  Acentra Health exists to empower better health outcomes through technology, services, and clinical expertise. Our mission is to innovate health solutions that deliver maximum value and impact. 

Lead the Way is our rallying cry at Acentra Health. Think of it as an open invitation to embrace the mission of the company; to actively engage in problem-solving; and to take ownership of your work every day. Acentra Health offers you unparalleled opportunities. In fact, you have all you need to take charge of your career and accelerate better outcomes – making this a great time to join our team of passionate individuals dedicated to being a vital partner for health solutions in the public sector. 

Acentra is looking for a Director of Software Quality Assurance to join our growing team.

Job Summary:

The role of the Software Quality Assurance, Director is to use Software...