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11 часов назад

Program Manager, New Product Development

88 000 - 110 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Program Manager, New Product Development (Consumer Healthcare and Wellness Products): Managing electromechanical consumer and medical-device development programs from concept to production with an accent on technical feasibility, supplier coordination, regulatory documentation, and risk management. Focus on planning global cross-functional programs, conducting design reviews and FMEA, maintaining Design History Files, and delivering products within budget, schedule, and quality constraints.

Location: Marlborough, Massachusetts, USA; hybrid schedule with 3 days onsite. International travel to Europe and Asia is required at 15%, along with early morning or evening availability for international calls.

Salary: $88,000–$110,000 annually, plus bonus.

Company

hirify.global is a global consumer products company managing 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.
  • Coordinate suppliers and global cross-functional teams across the US, Europe, and China.
  • Assess technical feasibility, manage budgets and schedules, and track program risks, costs, quality, and performance.
  • Create product specifications and documentation, including Design History Files.
  • Provide guidance on technical solutions and conduct design reviews, FMEA, and risk assessments.
  • Track vendor commitments, coordinate submittals, and troubleshoot issues to keep programs on schedule.

Requirements

  • Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or an equivalent field.
  • 3+ years of experience in consumer goods, medical devices, or another regulated industry.
  • Technical knowledge of plastic part design, electronics, firmware, and software used in consumer products.
  • Experience delivering multiple programs within budget and schedule constraints, with strong organization and communication skills.
  • Working knowledge of FDA, ISO, UL, and Design History Files; basic CAD knowledge; proficiency in Microsoft Office.
  • Must be authorized to work full-time in the United States.

Nice to have

  • Working knowledge of IEC 62304.
  • Understanding of medical-device safety requirements and regulatory submissions under European MDD/MDR and US FDA frameworks.
  • Familiarity with Agile processes.

Culture & Benefits

  • Flexible hybrid work model with remote work typically available on Mondays and Fridays.
  • Healthcare, dental, and vision coverage.
  • Paid holidays, paid parental leave, paid time off, and paid charitable leave.
  • 401(k) with company match, life insurance, and short- and long-term disability coverage.
  • Educational assistance and bonus eligibility.

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