Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
Очень мало
$89к-125к/год
$140к$170кмедиана$190к
По похожим ролям (49) ~ $170к/год
70
Хорошая вакансия
развернуть
Роль описана четко и дает серьезную ответственность за международные продуктовые программы, но требуется право на работу в США и регулярные поездки.
Кликните для подробной информации
Зарплата ниже рынкаТолько с правом на работу в СШАПонятная зона ответственностиМеждународные проектыПоездки за границу
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Program Manager (Healthcare & Wellness): Managing global healthcare and wellness new product development programs from concept to production with an accent on consumer electromechanical products, technical feasibility, regulatory documentation, and supplier coordination. Focus on assessing technical alternatives, managing risks and budgets, and delivering products within schedule and quality constraints.
Location: Marlborough, Massachusetts, USA; hybrid schedule with 3 days onsite and remote work on Mondays and Fridays. Must be authorized to work in the United States on a full-time basis. International travel of 15% is required.
Base salary: $88,743.78–$125,000 annually in Massachusetts, plus bonus.
Company
hirify.global is a global consumer products company developing wellness and healthcare products across brands including Honeywell, PUR, Braun, and Vicks.
What you will do
Plan, schedule, and execute healthcare and wellness New Product Development programs from concept through production with suppliers and internal teams.
Drive program progress using the New Product Development process, managing risks, budgets, schedules, costs, quality, and performance.
Coordinate global cross-functional teams and vendors across the United States, Europe, and China.
Create and maintain product specifications, program documentation, Design History Files, and records required by regulatory and quality systems.
Coordinate vendor commitments and submittals while overseeing delivery of quality products.
Requirements
Bachelor’s degree in mechanical, electrical, biomedical engineering, or equivalent.
7+ years of experience in consumer goods, medical devices, or an equivalent regulated industry.
Experience designing and manufacturing consumer and/or medical devices.
Technical knowledge of plastic part design, electronics, firmware, and software used in consumer products.
Proven program management experience with strong organization and attention to detail; ability to deliver within budget and schedule constraints.
Leadership, teamwork, communication, independent working, flexibility, and ability to manage multiple programs.
Ability to collaborate with global vendors, coordinate submittals, track commitments, and oversee product quality.
Proficient in Microsoft Office programs, including Excel, Project, Outlook, and Word.
Working knowledge of FDA, ISO, UL, and Design History Files; basic knowledge of CAD.
Authorization to work in the United States on a full-time basis.
Nice to have
Working knowledge of IEC 62304.
Understanding of safety requirements and medical device regulatory submissions in Europe under MDD/MDR and in the USA under FDA requirements.
Familiarity with Agile processes.
Culture & Benefits
Flexible hybrid work model with in-office collaboration Tuesday through Thursday.
Healthcare, dental, vision, life insurance, short- and long-term disability coverage, and 401(k) with company match.
Paid holidays, parental leave, paid time off, and paid charitable leave.
Educational assistance and salary plus bonus.
Inclusive workplace focused on collaboration, innovation, and employee development.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →