Sr Manager Quality

5 days ago

Mississauga, Canada 2105 Merge Canada Holdco Unlimited Liability Company Full time

Sr Manager Quality & Continuous Improvement page is loaded Sr Manager Quality & Continuous Improvement Apply remote type Hybrid locations Mississauga, Ontario Hartland, Wisconsin time type Full time posted on Posted 3 Days Ago job requisition id JR00916

Join a team dedicated to supporting the crucial mission of improving health outcomes.

At Merative, you can apply your skills – and grow new ones – with colleagues who have deep expertise in health and technology. Merative provides data, analytics and software for the health industry. Our clients include providers, health plans, employers, life sciences companies and governments around the world. With industry-leading products and focused innovation, we help customers improve decision-making and performance so that together, we drive real progress in health. Learn more at merative.com

This role can be based in either Hartland, WI or Mississauga, Ontario.

The Sr Manager, Quality & Continuous Improvement is responsible for driving continuous improvement and delivering a Quality Management System (QMS) that enables the success of Merge Healthcare’s business while maintaining compliance. This is a leadership role that requires in-depth knowledge of quality management systems for regulated and non-regulated software in the healthcare technology sector. This role requires leadership and collaboration skills, with the ability to influence change and drive improvement at all levels of the organization.

Essential Job Duties

  • Quality Management Systems

    • Deliver an efficient and effective Quality Management System in conformance with applicable regulations, standards, and industry guidance

    • To enable Merge Healthcare to conduct business in target geographies, including USA, Canada, EU, and UK.

    • Provide leadership for internal, external, and supplier audits to identify areas for improvement, and implement corrective and preventive actions.

    • Proactively review and evaluate evolving regulations, standards, and industry guidance to maintain alignment of the organization with the “state of the art”.

    • Deliver effective training and education for employees to ensure awareness and understanding of QMS processes applicable to their role.

    • Plan and execute quality assurance processes, including Audit, CAPA, Change Control, Computer System Validation, Document/Record Control, Supplier Management, and Training.

    • Advise and coach employees on the application of the QMS, as necessary.

  • Continuous Improvement

    • Foster a culture of excellence, collaboration, and continuous improvement across the organization.

    • Collaborate with cross-functional business and functional leaders

      • Drive continuous improvement initiatives to enhance the efficiency and effectiveness of the QMS.

      • Define, collect, analyze, and track quality metrics to monitor performance and provide recommendations for improvement.

      • Generate reports and recommendations for improvement as input to Management Reviews at prescribed intervals.

  • Leadership

    • Lead and mentor a high-performing team of direct reports, fostering a culture of collaboration and continuous learning.

    • Establish clear performance expectations and goals for the team, providing regular feedback, coaching, and recognition.

Basic Qualifications

  • Proven experience (7+ years) in the healthcare technology or life sciences industry, preferably with a focus on Software as a Medical Device (SaMD).

  • Exceptional problem-solving and decision-making skills.

  • Strong organization and management skills, with the ability to prioritize, multi-task, and delegate to achieve established goals and objectives.

  • Excellent interpersonal, communication, and presentation skills.

Technical Skills

  • In-depth understanding of applicable standards, including ISO13485, ISO14971, and IEC62304.

  • Knowledge of applicable regulations preferred:

    • 21 CFR Part 820 US Quality Management System Regulation

    • SOR/98-282 Canada Medical Device Regulation, a

    • 2017/745 EU Medical Device Regulation

  • Understanding of Software as a Medical Device (SaMD) and software development lifecycles, including agile methods.

  • Familiarity with technology applications, such as Jira, Confluence, TrackWise Digital, and Microsoft 365.

Supervisory Skills

  • At least 5 years management experience in a medium to large-sized organization.

  • Track record of building and leading high-performance teams.

  • Ability to work independently with minimal supervision in a team setting.

Education Requirements

  • Bachelor’s degree in a scientific or technical discipline required.

  • Certified ISO13485 Lead Auditor preferred.

Work Environment

The work environment characteristics here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Office environment, or remote work-from-home.

  • Travel: ~10%

About Us

Merative is a place to grow. We offer opportunities to apply your skills — and develop new ones — with colleagues who have deep expertise in health and technology. At Merative we’re driven and professional, but treat each other with compassion and respect. Roles at Merative include product design and development, technology innovation, product and account management, sales and consulting, communications and marketing, management, operations and more. 

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