11 часов назад
Program Manager, New Product Development
88 000 - 110 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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