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
QualityHub is a consulting organization that serves the FDA regulated industry, primarily manufacturers of Medical Devices and Pharmaceuticals. Our focus is on client adherence to FDA regulations, particularly the Good Manufacturing Practices (GMPs) and/or Quality Systems for Medical Devices and Pharmaceuticals. Our clients are worldwide, and range in size from $50 Million to $40 Billion in annual sales. We use ex-FDA and ex-industry experts to perform audits and provide consulting in order to teach, coach and guide our clients into the understanding and implementation of the various FDA legal requirements.
Through consulting and auditing, we assist clients with complex situations that may involve FDA Warning Letters, recalls, due diligence, risk management, new product development and launch, FDA legal actions and other high-risk activities. We also help optimize and improve quality systems.
Additionally, we service our clients by providing Interim Professionals (IP). The IPs are temporary staff personnel who work in various positions in the companies to help out during key projects, or when vacancies leave a position open. The IP can fill the roles of Interim Vice President all the way down to interim Professional Staffer, and numerous positions in-between, such as Interim Team Leader, Interim Manager and Interim Director.