Clicking Apply Now takes you to AutoApply where you can tailor your resume and apply.
Experience Level
Senior Level Manager
Qualifications
Proven experience in quality assurance management, preferably in a technology-driven environment. Strong understanding of quality control methodologies and tools. Excellent leadership and team management skills. Ability to communicate effectively across all levels of the organization. Bachelor's degree in Engineering, Quality Management, or a related field.
About the job
The Director of Quality Assurance at Alten Technology USA guides quality standards across all projects and services. This position holds responsibility for shaping and refining policies, processes, and systems that support consistent, reliable outcomes for clients.
Role overview
This leadership role focuses on maintaining and improving quality assurance practices throughout the organization. The Director works to ensure that quality expectations are met and that processes align with the company’s goals.
Key responsibilities
Lead the development and implementation of quality assurance policies and procedures
Oversee systems that monitor and uphold quality across projects and services
Support the company’s commitment to delivering results for clients
Location
This position is based in Conklin, New York, United States.
About Alten Technology USA
Alten Technology USA is a leading provider of engineering and technology consulting services. We pride ourselves on our commitment to innovation, quality, and customer satisfaction. Our team comprises skilled professionals dedicated to pushing the boundaries of technology and delivering exceptional results.
Join WelbeHealth as the Director of Quality Operations, where you will lead initiatives to enhance the quality and efficiency of our healthcare services. In this pivotal role, you will be responsible for developing and implementing quality improvement strategies that align with our mission to provide exceptional care to our patients.
Full-time|$193.6K/yr - $244.5K/yr|Hybrid|Northbridge, MA
Role overview The Director of Quality Operations oversees global GMP quality at Eyepoint Pharmaceuticals, supporting both internal and external manufacturing. This position plays a key role in development and commercial programs, ensuring quality standards are consistently met across all operations. Reporting to the Senior Director of Global Quality Assurance, the Director leads both the Quality Operations and Quality Engineering teams. Daily responsibilities include providing direct support for quality-related activities and guiding team efforts to maintain compliance and operational excellence. Location and schedule This role is based at the Northbridge, MA facility. The company offers a hybrid work arrangement, requiring at least three days per week on-site. During major project milestones, on-site presence may be needed more frequently. The position also involves regular travel to the Watertown location, typically one to two times per week. Occasional travel to external partner sites is expected, accounting for approximately 5-10% of the time.
We are seeking a highly skilled and experienced Director of Clinical Quality to join our dynamic team at Integrated Resources, Inc. In this pivotal role, you will be responsible for overseeing the clinical quality management systems, ensuring compliance with regulatory standards, and driving continuous improvement in clinical processes.Your leadership will be vital in fostering a culture of quality and safety, collaborating with multidisciplinary teams to enhance patient outcomes and operational efficiency.
As the Director of Quality Assurance at dstaff, you will spearhead our commitment to excellence by overseeing all quality-related initiatives. Your leadership will ensure that our products and services meet the highest standards of quality and compliance. You will collaborate closely with cross-functional teams to develop and implement quality assurance processes that enhance our operational efficiency and customer satisfaction.
Full-time|$184K/yr - $214K/yr|On-site|San Carlos, California, United States
Join Our Mission to Safeguard Humanity!Vaxcyte is at the forefront of clinical-stage vaccine innovation, dedicated to developing high-fidelity vaccines aimed at protecting humanity from the serious and costly implications of bacterial diseases. Our commitment to eradicating or treating infections such as invasive pneumococcal disease, Group A Strep, and Shigella exemplifies our mission. With a clear and well-defined path to success, Vaxcyte is poised to make a significant impact. Our Approach: At Vaxcyte, what we do is as crucial as how we do it. Our collaboration is anchored in four enduring core values: *Rethink Convention: We infuse creativity and diverse thinking into every aspect of our work to continuously innovate how vaccines are delivered. *Aim High: We embrace our bold collective goal to courageously develop the most complex biologics ever attempted to safeguard humanity. *Lead with Heart: Every individual at Vaxcyte leads with a kindness-first, inclusive approach that fosters collaboration and vigorous debate to advance our business objectives. *Model Excellence: The scale of our challenge necessitates a shared commitment to integrity, accountability, equality, and transparency in communication and decision-making.Position Overview:The Associate Director of Quality Control Operations is a pivotal executive role within our global vaccine organization. This position is responsible for implementing Vaxcyte's analytical strategies at our Contract Development and Manufacturing Organizations (CDMOs) and Contract Research Organizations (CROs). Acting as the primary liaison for our CDMOs and CROs, you will ensure the delivery of high-quality, accurate, and compliant testing and analytical services. Collaborating closely with the analytical technical lead and various functions—including Analytics, Process Development, Manufacturing Science, Quality Assurance, and Regulatory Affairs—you will provide leadership and oversight for the execution of analytical strategies supporting analytical readiness and deliverables. You will be accountable for ensuring timely and compliant testing and release at our CDMO and CRO, facilitating a secure and uninterrupted supply of Vaxcyte’s groundbreaking therapies.
We are seeking a Director of Quality Management to lead our quality assurance initiatives at mach. In this pivotal role, you will be responsible for developing and implementing quality management strategies, ensuring compliance with industry standards, and fostering a culture of continuous improvement within the organization. You will work closely with cross-functional teams to deliver high-quality products and services that meet customer expectations.
We are seeking a highly skilled Director of Quality Systems to lead our quality assurance initiatives and ensure compliance with industry standards. The ideal candidate will possess exceptional leadership skills and a deep understanding of quality systems within a dynamic environment.As the Director of Quality Systems, you will be responsible for developing, implementing, and maintaining quality management systems, ensuring that all products meet both regulatory and customer requirements. You will collaborate with cross-functional teams to drive continuous improvement and foster a culture of quality throughout the organization.
Full-time|On-site|Pine Bluff, Arkansas, United States
Central Moloney, Inc. manufactures distribution transformers and transformer components, operating from its headquarters in Pine Bluff, Arkansas since 1949. The company holds ISO 9001 certification and prioritizes product quality and reliable service. Role overview The Quality Director leads quality management at the Transformers AR facility in Pine Bluff. This onsite, salaried position shapes the company’s quality strategy and ensures ongoing compliance with ISO standards. Supporting continuous improvement is a central focus, with direct influence on both daily operations and long-term planning. Main responsibilities Develop and maintain quality management systems (QMS) that align with ISO standards and customer requirements. Set and implement quality strategies, policies, and procedures to improve product quality. Plan and conduct audits to assess the QMS and identify opportunities for improvement. Monitor regulatory and industry standards to ensure compliance. Lead, mentor, and support the quality control team, encouraging a culture of continuous improvement. Collaborate with cross-functional teams, including Engineering, to integrate quality standards throughout the product lifecycle. Facilitate root cause analysis and implement corrective and preventive actions for quality issues. Oversee documentation and record-keeping to track and report on quality metrics. Develop and manage training programs to build quality awareness and skills across the workforce. Stay current with industry best practices, new technologies, and trends in quality management. Work location This position is based onsite at the Transformers AR facility in Pine Bluff, Arkansas. FLSA status Salary Exempt
Full-time|$210K/yr - $230K/yr|Remote|Remote with up to 10% global and domestic travel
Position Summary Angitia is on the lookout for a seasoned and visionary Director of Quality Assurance and Quality Systems to play a pivotal role in our Quality Leadership Team. This individual will spearhead the development, execution, and ongoing enhancement of Angitia's GxP Quality Systems. The Director will be responsible for the implementation and upkeep of our electronic Quality Management System (eQMS), acting as the business process owner for essential modules, including document control, training, deviations, CAPA, and change control. This role is crucial in driving the evolution of our Quality Systems and processes to ensure readiness for global pivotal clinical studies while maintaining inspection-ready Quality Systems that support clinical development, external manufacturing, and adapting regulatory expectations. The ideal candidate will possess extensive experience working in a dynamic, resource-constrained biotech environment, demonstrating a passion for building scalable processes, fostering cross-functional collaboration, and enhancing the culture of quality as the organization advances toward late-stage clinical development and commercialization.
At Crescent Biopharma, we aspire to transform the landscape of oncology by developing cutting-edge therapies tailored for cancer patients. Our innovative pipeline includes a leading PD-1 x VEGF bispecific antibody, alongside state-of-the-art antibody-drug conjugates. By harnessing diverse therapeutic modalities and established targets, we aim to expedite the development of potentially groundbreaking treatments, whether as standalone interventions or in combination therapies targeting various solid tumors. For more insights into our mission and vision, visit our website and connect with us on LinkedIn and X.We are currently in search of an Associate Director or Director of Analytical & GMP Quality Assurance Operations. In this pivotal role, you will oversee and guide the QA functions related to analytical development, quality control operations, and GMP quality activities across our clinical-stage biologics and ADC programs. Collaboration with cross-functional teams, including CMC, Analytical Sciences, Quality Control, and Technical Operations, as well as external manufacturing and testing partners, will be key to ensuring compliance with phase-appropriate GMP standards, maintaining data integrity, and ensuring inspection readiness within a dynamic outsourced operational framework. Your strategic vision will be instrumental in shaping Crescent's analytical quality strategy and driving the disciplined execution of core quality systems that align with our aggressive development timelines.
The Director of Clinical Quality at Lindus Health will play a central role in strengthening clinical operations and elevating patient care standards across the organization. This position is based in the US and focuses on driving quality initiatives that support safe, effective, and compliant healthcare delivery. Key responsibilities Lead initiatives to improve patient outcomes and uphold high standards within clinical teams. Ensure all practices comply with healthcare regulations and internal policies. Develop, monitor, and analyze quality metrics to assess clinical performance. Conduct audits to pinpoint areas for improvement and address gaps in care or processes. Design and deliver training programs to foster a culture of quality among staff. Work closely with multidisciplinary teams to implement evidence-based practices and support clinical excellence. Requirements Strategic approach and experience in clinical quality improvement. Ability to collaborate with professionals from diverse clinical and operational backgrounds. Strong knowledge of healthcare regulations and quality standards.
Full-time|On-site|Scottsdale, Arizona, United States
Join Axon, a leader in law enforcement technology, as the Director of Manufacturing Quality. In this pivotal role, you will oversee quality assurance processes to ensure our products meet the highest standards of excellence. You will lead a dedicated team, implement quality control measures, and collaborate across departments to drive continuous improvement.
We are seeking a dedicated and experienced Director of Quality Control to lead our quality assurance efforts at Crusoe. In this critical role, you will be responsible for developing, implementing, and maintaining quality control processes that ensure our products meet exceptional standards. You will collaborate with cross-functional teams to drive continuous improvement initiatives and foster a culture of quality throughout the organization.
We are seeking a dedicated and experienced Director of Clinical Quality to join our dynamic team at dstaff in Seattle, Washington. This role is pivotal in ensuring the highest standards of clinical care and quality assurance across our services. As the Director, you will lead initiatives to enhance patient safety, improve clinical outcomes, and ensure compliance with industry standards.Your leadership will influence critical decision-making processes and drive quality improvement strategies. Engage with cross-functional teams to foster a culture of excellence and continuously monitor performance metrics.
The future of AI — whether in training or evaluation, classical ML or agentic workflows — hinges on the availability of superior data.At HumanSignal, we are pioneering the platform that fuels the creation, curation, and evaluation of high-quality data. Our tools facilitate everything from fine-tuning foundational models to validating agent behaviors in production, empowering leading AI teams to ensure models are anchored in real-world signals rather than noise.Our open-source product, Label Studio, has emerged as the de facto standard for labeling and evaluating data across various modalities — encompassing text, images, time series, and agents in environments. With over 250,000 users and hundreds of millions of labeled samples, it stands as the most widely adopted OSS solution for teams dedicated to building AI systems.Label Studio Enterprise builds on this momentum by incorporating the security, collaboration, and scalability features essential for supporting mission-critical AI pipelines — from model training datasets to evaluation test sets and continuous feedback loops. As we advance in an era where AI is reshaping industries, we are excited to invite candidates who are eager to assist premier AI teams in constructing smarter and more accurate systems.We are looking for a Quality Operations Lead to uphold exceptional data quality across our Label Studio platform and Data Creation Laboratory operations. In this pivotal role, you will serve as the ultimate authority on the integrity and utility of the data we create and deliver to our clients. You will lead accountability across our most impactful projects, addressing complex quality challenges while spearheading strategic initiatives that ensure reliable and scalable delivery as we expand.Our Data Creation Laboratories go beyond labeling existing data; we engineer purpose-built datasets from the ground up in controlled settings. This elevates the quality control process: you won’t just be verifying annotations; you will ensure that the human-generated data we produce meets the rigorous standards demanded by cutting-edge AI laboratories and enterprises pushing the boundaries of innovation.
Full-time|$244K/yr - $308K/yr|On-site|New York, New York
Role Overview Peloton is seeking a Director of Global Product Quality based in New York, NY. This leader shapes and advances the company’s global product quality strategy, ensuring every product meets regulatory requirements, customer expectations, and Peloton’s own quality standards in every market. The Director works across functions, including design, manufacturing, supply chain, and post-market surveillance, to drive quality initiatives and foster a culture of compliance, excellence, and ongoing improvement worldwide. Key Responsibilities Develop and execute a global product quality strategy in line with Peloton’s corporate objectives. Set and maintain quality standards, policies, and performance metrics for all regions. Serve as executive sponsor for quality improvement and transformation programs. Lead quality governance forums and present quality performance updates to senior leadership. Embed quality practices throughout the product lifecycle, from concept and design through manufacturing, distribution, and post-market activities. Oversee risk management processes, including FMEA, CAPA, root cause analysis, and change control. Monitor and improve key quality indicators such as defect rates, cost of poor quality (COPQ), customer complaints, and field performance. Advocate for customer feedback in product development and manufacturing processes. Manage complaint handling, field actions, and corrective and preventive action programs. Work closely with Commercial and Customer Service teams to resolve quality issues quickly. Partner with Product Management, Engineering, Operations, Supply Chain, Member Support, and Procurement to maintain supplier quality assurance and product integrity. Support supplier quality initiatives, including qualification, auditing, performance monitoring, and remediation. Align global quality teams to ensure consistency across all regions. Build, mentor, and develop a high-performing global quality organization. Promote a culture of accountability, transparency, and continuous improvement. Implement succession planning and talent development programs within the quality function.
Full-time|On-site|3200 Fruit Ridge Ave, Walker, MI 49544
About Us:At Challenge Manufacturing, our commitment to operational excellence is driven by our employee-owners. As a premier tier 1 supplier of intricate metal assemblies for the global automotive sector, we are at the forefront of innovative solutions for future mobility. We believe that the most effective ideas emerge from diverse perspectives, and it is this unique combination of insights and the collaborative spirit of our industry leaders that enables us to tackle any challenge. Our team takes immense pride in our work and exemplifies our core values of safety, ownership, and teamwork every day; they are the true engine behind our operations.Challenge is honored to be recognized as one of the largest employee-owned automotive firms in North America. One of the many advantages of becoming part of the Challenge team is our Employee Stock Ownership Plan (ESOP). This program allows us to distribute shares of the company to all employee-owners annually, providing an additional retirement benefit that grows throughout your career at Challenge. Being a part of an ESOP means our employee-owners share in the success of Challenge!We are proud to be #QualityDriven and #PeoplePowered!Our Ideal Candidate:We are on the lookout for a Director of Advanced Quality who will spearhead Challenge Manufacturing’s product launch quality strategy across various programs and clients. This role is pivotal in ensuring that all Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP) requirements are met with world-class standards, thereby supporting excellence in launch and long-term customer satisfaction.As a vital leader within a Tier 1 automotive supplier, this individual will foster cross-functional collaboration among Quality, Program Management, Engineering, Manufacturing, and Suppliers to ensure adherence to IATF 16949, customer-specific requirements, and OEM expectations. The ideal candidate is an experienced automotive quality professional who thrives in dynamic, fast-paced environments and consistently achieves measurable results in launch performance and customer quality metrics.
Full-time|$70K/yr - $90K/yr|On-site|Unit C, 220 W Campus Drive, Arlington Heights, 60004
Are you ready to spearhead the comprehensive inspection and quality control operation for a diverse range of products, ensuring excellence for millions of customers? If you have a passion for quality and leadership, this is the perfect opportunity for you.About Lily & Fox:Lily and Fox is a rapidly expanding direct-to-consumer beauty brand, renowned for offering the world's largest selection of nail wraps. We ship millions of orders globally using Shopify, Shipstation, and our proprietary technology. Our mission is to make beauty accessible and affordable, setting a new standard in the nail industry with unparalleled quality and variety.Position Overview:As the Head of Quality Control, you will oversee the entire inspection and quality control operation. You will lead a dedicated team responsible for hand-inspecting millions of products annually and collaborate directly with suppliers to uphold our rigorous standards.Your role includes hiring, coaching, and managing team performance, ensuring daily productivity goals are met. You will set clear expectations, conduct visual inspections, mentor your team on best practices, audit their work, and maintain a balance between throughput and quality. Familiarity with Standard Operating Procedures (SOPs), checklists, training programs, and AQL-style audits for final product verification will be essential. You will also analyze customer feedback, drive process improvements, and work closely with our Customer Service, Fulfillment, Inventory Planning, and Manufacturing teams.This is a full-time, on-site position.
Full-time|On-site|Conklin, New York, United States
The Director of Quality Assurance at Alten Technology USA guides quality standards across all projects and services. This position holds responsibility for shaping and refining policies, processes, and systems that support consistent, reliable outcomes for clients. Role overview This leadership role focuses on maintaining and improving quality assurance practices throughout the organization. The Director works to ensure that quality expectations are met and that processes align with the company’s goals. Key responsibilities Lead the development and implementation of quality assurance policies and procedures Oversee systems that monitor and uphold quality across projects and services Support the company’s commitment to delivering results for clients Location This position is based in Conklin, New York, United States.
Join our team as the Director of Construction Quality at AECOM in Cleveland, where you will lead our quality assurance initiatives across diverse construction projects. Your expertise will guide teams in implementing best practices, ensuring high standards of quality and compliance throughout various stages of construction.
