Quality Matters (QM) is the global organization leading quality assurance in online and innovative digital teaching and learning environments. It provides a scalable quality assurance system for online and blended learning used within and across organizations. When you see QM Certification Marks on courses or programs, it means they have met QM Course Design Standards or QM Program Review Criteria in a rigorous review process.
A member-based non-profit organization, QM is one of the largest providers of assessed professional development for online faculty. While many organizations offer “sit and get” webinars or issue certificates of completion for lightly-facilitated workshops, QM courses and workshops feature rigorous assessments and robust facilitation. This professional development supports QM quality assurance at the member organization and throughout the QM community.
QA Consultants is North America’s largest software quality engineering services firm. An award-winning onshore provider of software testing and quality assurance solutions, we are the trusted engineering services company for business, industry and government supported by leading practitioners and solutions.
For almost 30 years, we have successfully delivered 12,000+ mission-critical projects in the private, public and not-for-profit sectors. We reduce risk and improve time to market with quality engineering, keep applications secure through dedicated application security capabilities, and reduce cost of ownership while enabling applications to scale via performance engineering. We are proud of our vision to help clients achieve flawless technology outcomes.
QA Consultants also operates a robust emerging technologies practice with a focus on quality engineering solutions for connected and autonomous vehicles, artificial intelligence (AI), Internet of Things (IoT) and blockchain.
CAREERS
Please visit the Careers pages on our website to learn more. We just might have the perfect employment opportunity for you.
careers.qaconsultants.com
Since 2004, QualityHub has helped Medical Device, Pharmaceutical, Biologics, and Combination Product companies stay inspection-ready, close quality system gaps, and build compliance that lasts.
QualityHub was founded by former FDA officials, and our leadership team brings more than 70 years of combined FDA experience, from field investigations to CDRH’s Office of Compliance. Our consultants include engineers, scientists, physicians, nurses, and former industry quality and regulatory leaders. We know how FDA inspects and how your operation actually runs.
👉 How We Help
• Inspection Readiness: mock FDA inspections, quality system and supplier audits, SME and response team training, and on-site inspection support
• Remediation: FDA-483, Warning Letter, and Consent Decree response, CAPA, and remediation program management
• Quality Systems: QMSR (21 CFR 820), ISO 13485, ISO 14971 risk management, design controls, validation, and drug GMP
• Regulatory & Clinical: regulatory compliance strategy, EU MDR, MDSAP, and clinical consulting
• Product Development & Project Management
👉 On-Demand Talent
Interim executives, SMEs, and professionals in QA, RA, Clinical, R&D, Manufacturing & Operations, Supply Chain, and Program/Project Management.
Employee-owned and headquartered in Orlando, QualityHub supports clients across the US and internationally, and many have worked with us for years.
👉 Visit QualityHub.com or message us to start the conversation, and subscribe to QHub Insights, our monthly e-zine, for practical inspection and compliance guidance.