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
The Sr Manager, Design Quality is responsible for collaborating with cross-functional teams to promote the safety, quality, reliability, and compliance of Merge Healthcare’s products. This is a senior leadership role with responsibility for managing a team of Quality Engineers focused on guiding the delivery of regulated and non-regulated medical imaging software systems. The Sr Manager, Design Quality role requires in-depth knowledge of the product development lifecycle, design controls, safety and cybersecurity risk management, and usability. This role requires a strong leader with exceptional collaboration, critical-thinking, and problem-solving skills, and the ability to drive cross-functional improvement at all levels of the organization.Essential Job Duties
Plans, directs, and implements the design quality aspects of Merge Healthcare’s design and development of new medical imaging solutions, with a focus on software quality/reliability, risk management (patient safety and cybersecurity), and usability.
Provides expertise and guidance in interpreting applicable regulations and industry standards.
Ensures development programs are appropriately planned and resourced for design quality.
Proactively identifies, prioritizes, communicates, and resolves quality, safety, and compliance issues.
Provides oversight, training, and coaching in the application of Quality Management System (QMS) processes to ensure successful adoption and implementation by product development teams.
Supports development of deliverables for regulatory submissions.
Assists with post-market activities, including Health Hazard Evaluations (HHEs), field corrections, and post-market surveillance, as necessary.
Participates in internal and external audits and inspections, as necessary.
Drives continuous improvement of Merge Healthcare’s processes to advance quality, safety, and compliance.
Provides oversight for the development and improvement of quality programs, systems, processes, and procedures to ensure compliance with applicable regulation and standards.
Fosters a culture of excellence, collaboration, and continuous improvement across the organization.
Leads and mentors a high-performing team of direct reports, fostering a culture of collaboration and continuous learning.
Establishes clear performance expectations and goals for the team, providing regular feedback, coaching, and recognition.
Collaborates with cross-functional business and functional leaders to drive continuous improvement initiatives to enhance the efficiency and effectiveness of the QMS.
Defines, collects, analyzes, and tracks quality metrics to monitor performance and provide recommendations for improvement.
Generate reports and recommendations for improvement as input to Management Reviews at prescribed intervals.
Basic Qualifications
Proven experience (10+ years) in healthcare technology, life sciences, or similar regulated industries, preferably with a focus on Software as a Medical Device (SaMD).
Exceptional collaboration, problem-solving, critical-thinking, 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, IEC62304, and IEC62366.
Knowledge of applicable regulations preferred:
21 CFR Part 820 US Quality Management System Regulation
SOR/98-282 Canada Medical Device Regulation
2017/745 EU Medical Device Regulation
In-depth understanding of Software as a Medical Device (SaMD) and software development lifecycles, including agile methods.
Familiarity with technology applications, such as Jira, Aha!, Jama, and Microsoft 365.
Supervisory Skills
At least 5 years’ technical leadership or 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, or equivalent experience.
Experience with agile development and cloud solutions 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%
It is the policy of Merative to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Merative will provide reasonable accommodations for qualified individuals with disabilities.
Merative participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees
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