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22 часа назад

Senior Director VET Quality (Orthopaedics)

196 000 - 342 700$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
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
Senior Director VET Quality (Orthopaedics) (Medical Devices and Quality Engineering): Leading end-to-end quality for new orthopaedic products, development processes, transfers, and supply chain activities with an accent on cross-functional leadership, compliance, and strategic decision-making. Focus on resolving complex quality issues, integrating enabling technologies across platforms, and ensuring products reach the market compliantly.

Location: Raynham, Massachusetts, United States of America; additional posting location: Palm Beach Gardens, Florida, United States of America

Base pay range: $196,000–$342,700 per year

Company

Johnson & Johnson MedTech’s Orthopaedics business, DePuy Synthes, develops solutions for joint reconstruction, trauma, spine, sports medicine, and related surgical technologies.

What you will do

  • Lead the Quality organization for the VET Platform, with accountability for design and Supply Chain Quality.
  • Own end-to-end quality for new products and processes developed with R&D, including transfers to internal and external supply chain partners.
  • Lead global, cross-functional, multidisciplinary project teams and define product development and production improvement strategies.
  • Provide direction, structure, and decision-making in high-risk, ambiguous situations.
  • Build partnerships across Supply Chain, R&D, Regulatory, Business Development, commercial organizations, and service teams.
  • Lead resolution of cross-functional issues and communicate compliance matters and opportunities to senior management.

Requirements

  • Bachelor’s degree or equivalent.
  • At least 5 years of Quality Engineering experience in new product development, Supply Chain, or both.
  • Experience in the medical device and/or pharmaceutical industry; 12+ years is preferred.
  • Experience enabling technology and integrating it into multiple platforms.
  • Proven complex decision-making experience and a record of bringing compliant products successfully to market.
  • Strong analytical, critical-thinking, communication, organizational, leadership, and people-development skills.

Nice to have

  • Quality Management Systems, Quality Control, CAPA, SOPs, compliance management, and continuous improvement.
  • Experience developing and coaching people, inclusive leadership, performance measurement, and succession planning.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo.
  • Participation in pension, savings, and 401(k) plans.
  • Eligibility for the long-term incentive program.
  • Vacation, sick time, holidays, personal and family time, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time-off benefits.
  • International and cross-functional collaboration across the Orthopaedics organization.

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