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Quality System Compliance Manager - Medical Device

Оценка ИИ

Отличная позиция в глобальной инновационной компании с прозрачной вилкой зарплаты и расширенным пакетом льгот. Роль предлагает уникальный вызов на стыке MedTech и Consumer Electronics.


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Сложность вакансии

ЛегкоСложно
Оценка ИИ

Высокая сложность обусловлена необходимостью совмещать строгие медицинские стандарты (ISO 13485, FDA) с быстрыми темпами разработки потребительской электроники. Требуется глубокий опыт (7-10 лет) и умение внедрять цифровые QMS-решения.

Анализ зарплаты

Медиана145 000 $
Рынок125 000 $ – 175 000 $
Оценка ИИ

Предложенная зарплата ($131,900 — $161,200) полностью соответствует рыночным ожиданиям для позиции менеджера по комплаенсу в сфере медицинских изделий в США, находясь в пределах медианы для опытных специалистов.

Сопроводительное письмо

I am writing to express my strong interest in the Quality System Compliance Manager position for Medical Devices at SharkNinja. With over 8 years of experience in medical device quality systems and a proven track record of implementing ISO 13485 and 21 CFR Part 820 compliant frameworks, I am particularly drawn to SharkNinja’s vision of integrating QMS directly into high-velocity consumer electronics development. My background in managing MDSAP-aligned audits and my hands-on experience with digital tools like Greenlight Guru and Jira align perfectly with your "digital-first" approach.

Throughout my career, I have specialized in operationalizing compliance within fast-paced environments, ensuring that quality processes act as enablers for innovation rather than bottlenecks. I have successfully led cross-functional teams through complex regulatory landscapes, including EU MDR transitions and FDA inspections. I am eager to bring my expertise in risk management (ISO 14971) and embedded controls to SharkNinja to help scale your medical device portfolio while maintaining the highest standards of safety and compliance.

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Составьте идеальное письмо к вакансии с ИИ-агентом

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Присоединяйтесь к SharkNinja и возглавьте создание инновационной системы качества для медицинских девайсов будущего!

Описание вакансии

About Us 

SharkNinja is a global product design and technology company, with a diversified portfolio of 5-star rated lifestyle solutions that positively impact people’s lives in homes around the world. Powered by two trusted, global brands, Shark and Ninja, the company has a proven track record of bringing disruptive innovation to market and developing one consumer product after another has allowed SharkNinja to enter multiple product categories, driving significant growth and market share gains. Headquartered in Needham, Massachusetts with more than 4,100 associates, the company’s products are sold at key retailers, online and offline, and through distributors around the world.

Quality System Compliance Manager, Medical Devices 

As the Quality System Compliance Manager, Medical Devices, you will lead the design, implementation, and continuous improvement of SharkNinja’s Quality Management System (QMS) for medical devices. This role is accountable for ensuring regulatory compliance while deliberately shaping a QMS that works within a high-velocity, consumer electronics product development environment. 

You will establish a QMS that is integrated, digital-first, and ownership-driven—aligned to SharkNinja’s specification developer model and embedded directly into existing new product development (NPD) processes rather than operating as a parallel or centralized function. The role partners closely with Engineering, PMO, Quality, Regulatory, Legal, and Product teams to ensure quality is operationalized across the organization and supports rapid innovation and scale. 

Key Responsibilities 

  • Own and evolve the global Medical Devices Quality Management System (QMS), ensuring sustained compliance with 21 CFR Part 820 / QMSR, ISO 13485, MDSAP, and EU MDR, while enabling rapid, concurrent product development across multiple programs.
  • Establish QMS governance, decision rights, and escalation mechanisms to ensure consistent execution across products, programs, and geographies.
  • Maintain a risk-based, audit-ready QMS supporting development, commercialization, and lifecycle activities across North America, the EU, and MDSAP-participating markets.
  • Design a QMS aligned to SharkNinja’s consumer electronics NPD model, emphasizing embedded controls, simplified documentation, digital evidence, and distributed ownership rather than centralized quality gatekeeping.
  • Embed QMS into NPD Processes & Digital Tools: Integrate quality system requirements directly into existing workflows and platforms (e.g., PLM, Veeva, Greenlight Guru, Test Management tools, JIRA, eQMS), ensuring design controls, risk management, change management, and documentation are executed within standard development workflows with minimal manual overhead and clear, audit-ready digital evidence.
  • Lead and support internal audits, external audits, regulatory inspections, and management reviews, serving as the primary quality systems authority.
  • Oversee core QMS processes—including document control, NCRs, CAPAs, training, supplier quality management, post-market surveillance, and change management—and foster a quality culture where QMS activities are embedded into day-to-day execution and enable speed, clarity, accountability, and informed risk-taking.

Qualifications & Experience 

  • Bachelor’s or Master’s degree in Engineering, Life Sciences, Quality, or a related technical discipline.
  • 7–10+ years of experience in medical device quality systems, preferably within consumer electronics, electromechanical devices, or high-velocity product development environments.
  • Demonstrated experience designing, implementing, and operating QMS compliant with 21 CFR Part 820 / FDA QMSR, ISO 13485, EU MDR, within an MDSAP-aligned audit framework.
  • Strong hands-on experience with core QMS processes, including document control, CAPA, NCRs, audits, training, supplier quality management, and post-market surveillance.
  • Deep understanding of design controls and risk management for electromechanical medical devices, including ISO 14971, hazard analysis, DFMEA, and lifecycle risk management.
  • Strong cross-functional influence, communication, and stakeholder management skills in complex, matrixed organizations.
  • Pragmatic, systems-thinking mindset with a proven ability to operationalize QMS compliance in fast-paced, innovation-driven environments.

Salary and Other Compensation: The annual salary range for this position is displayed below. Factors which may affect starting pay within this range may include geography/market, skills, education, experience and other qualifications of the successful candidate. 

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, flexible spending accounts, health savings accounts (HSA) with company contribution, 401(k) retirement plan with matching, employee stock purchase program, life insurance, AD&D, short-term disability insurance, long-term disability insurance, generous paid time off, company holidays, parental leave, identity theft protection, pet insurance, pre-paid legal insurance, back-up child and eldercare days, product discounts, referral bonus program, and more.

Pay Range

$131,900—$161,200 USD

Our Culture

At SharkNinja, we don’t just raise the bar—we push past it every single day.  Our Outrageously Extraordinary mindset drives us to tackle the impossible, push boundaries, and deliver results that others only dream of. If you thrive on breaking out of your swim lane, you’ll be right at home.

What We Offer

We offer competitive health insurance, retirement plans, paid time off, employee stock purchase options, wellness programs, SharkNinja product discounts, and more. We empower your personal and professional growth with high impact Learning Programs featuring bold voices redefining what’s possible. When you join, you’re not just part of a company—you’re part of an outrageously extraordinary community. Together, we won’t just launch products—we’ll disrupt entire markets.  

At SharkNinja, Diversity, Equity, and Inclusion are vital to our global success. Valuing each unique voice and blending all of our diverse skills strengthens SharkNinja’s innovation every day. We support ALL associates in bringing their authentic selves to work, making an impact, and having the opportunity for career acceleration. With help from our leadership, associates, and our community, we aim to have equity be a key component of the SharkNinja DNA. 

Learn more about us:  

Life At SharkNinja  

Outrageously Extraordinary

SharkNinja Candidate Privacy Notice

We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, disability, or any other class protected by legislation, and local law. SharkNinja will consider reasonable accommodations consistent with legislation, and local law. If you require a reasonable accommodation to participate in the job application or interview process, please contact SharkNinja People & Culture at accommodations@sharkninja.com

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Создайте идеальное резюме с помощью ИИ-агента

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Навыки

  • ISO 13485
  • ISO 14971
  • FDA 21 CFR Part 820
  • EU-MDR
  • MDSAP
  • Quality Management System
  • CAPA
  • Risk Management
  • Internal Audit
  • Veeva
  • Greenlight Guru
  • Jira
  • PLM

Возможные вопросы на собеседовании

Проверка умения адаптировать жесткие стандарты под гибкие процессы компании.

Как бы вы интегрировали требования Design Controls в процесс разработки продукта, который движется со скоростью потребительской электроники?

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Опишите ваш опыт руководства внешней проверкой (например, аудит MDSAP или инспекция FDA). С какими основными трудностями вы столкнулись?

Проверка технических навыков в области управления рисками.

Как вы подходите к внедрению ISO 14971 в контексте электромеханических медицинских изделий?

Оценка лидерских качеств и влияния в матричной структуре.

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Проверка опыта работы с современным ПО для качества.

Каков ваш опыт работы с eQMS и PLM системами (например, Veeva или Greenlight Guru) для обеспечения цифровой прослеживаемости?

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Страна
США
Зарплата
131 900 $ – 161 200 $