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4 дня назад

Senior Manager Product Quality Management (MedTech)

122 000 - 212 750$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Senior Manager Product Quality Management (MedTech): Leading brand quality strategy and improvement across new product introduction, manufacturing, supply chain, R&D, regulatory, and customer experience with an accent on medical device quality, CAPA, validation, and long-term product planning. Focus on making quality decisions for product launches and changes, directing cross-functional engineering groups, improving manufacturing processes, and managing compliance and brand scorecard outcomes.

Location: Milpitas, California or Irvine, California, United States; up to 10% domestic and international travel required.

Salary: $122,000–$212,750 base pay; Bay Area range: $142,000–$244,950.

Company

Johnson & Johnson MedTech develops healthcare and medical device solutions across innovative medicine and MedTech.

What you will do

  • Lead brand quality monitoring, analysis, improvement, and communication from new product introduction through customer use.
  • Develop long-term quality plans addressing patient needs and measurable business outcomes.
  • Partner with R&D, Supply Chain, Quality Assurance, Regulatory, commercial teams, and regional offices on product performance and improvement strategies.
  • Assess new product launches and determine whether to accelerate, modify, or delay them based on product quality.
  • Lead manufacturing improvement strategies, overarching CAPAs, quality plans, control plans, major changes, and validations.
  • Make brand-wide quality decisions, including signatory authority for non-conformances and change controls.

Requirements

  • University or bachelor’s degree or equivalent required; a degree in statistics, engineering, or science is preferred.
  • 8+ years of experience in statistics, process engineering, or the medical device industry.
  • At least 3 years of experience in two of the following areas: R&D, manufacturing, and quality.
  • Thorough understanding of GMP, ISO, and validation regulations, with knowledge of NPI processes and statistical methods.
  • Demonstrated management, cross-functional leadership, mentoring, technical improvement, communication, and organizational skills.
  • Ability to build cost-savings and business-growth cases.

Nice to have

  • Advanced technical or MBA degree.
  • Technical understanding of manufacturing equipment and processes.
  • Experience in manufacturing, technical improvements, and statistical methods.

Culture & Benefits

  • Inclusive work environment focused on individual dignity, diversity, and merit.
  • Eligibility for pension and 401(k) savings plans.
  • Vacation, sick time, holiday pay, personal and family time, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time-off benefits.
  • Support for an inclusive interview process and applicant accommodations.

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