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11 дней назад

Associate Director Biosurgery R&D LCM (MedTech)

137 000 - 235 750$
Формат работы
hybrid
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
Associate Director Biosurgery R&D LCM (MedTech): Leading research and development lifecycle management projects for biosurgery products, including design changes, process changes, documentation, and regulatory submissions, with an accent on scientific direction, design controls, and process validation. Focus on directing cross-functional teams, mentoring R&D staff, maintaining scientific data quality, and delivering lifecycle improvements for hemostats, sealants, adhesives, and related surgical technologies.

Location: Raritan, New Jersey, United States; flex/hybrid schedule with 3 days per week on-site. Approximately 20% domestic and/or international travel is required. Relocation assistance may be available to uniquely qualified candidates.

Base pay: $137,000–$235,750 per year.

Company

Johnson & Johnson MedTech develops healthcare and surgical technologies designed to make treatments smarter, less invasive, and more personalized.

What you will do

  • Lead scientific direction for biosurgery R&D lifecycle management projects, including design changes, process changes, and base business support.
  • Oversee project portfolios, identify improvement opportunities, and ensure timelines and milestones are achieved.
  • Review design control documentation, verification and validation protocols and reports, claims support, regulatory submissions, and technical reports.
  • Evaluate R&D protocols for compliance with safety, efficacy, compatibility, industry, company, and regulatory expectations.
  • Present program updates to senior management and ensure the scientific integrity and quality of generated data.
  • Hire, develop, motivate, and mentor staff while leading cross-functional collaboration across R&D, Supply Chain, Quality, Regulatory, and commercial functions.

Requirements

  • BS in Engineering or Science is required; relevant fields include Chemical Engineering, Mechanical Engineering, Materials Science, Polymer Science, and Biomedical Engineering.
  • Significant R&D, lifecycle management, or related leadership experience in MedTech, medical devices, or healthcare is required.
  • 8+ years of people leadership experience, including cross-functional leadership and change management in dynamic, matrixed environments.
  • Knowledge of design controls and process validation principles and practices is required.
  • Excellent collaboration and influencing skills are required.
  • Experience in the medical device industry or medical field is required.

Nice to have

  • Advanced degree such as an MS or PhD.
  • Experience with biosurgery products such as hemostats, sealants, adhesives, or tissue scaffolds.
  • Knowledge of bioinformatics, biological engineering, biostatistics, or SAP Product Lifecycle Management.

Culture & Benefits

  • Inclusive work environment focused on respecting individual differences and dignity.
  • Retirement pension and 401(k) savings plans, subject to plan terms.
  • Vacation, sick time, holiday pay, personal and family time, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time-off benefits.
  • Accommodation support is available during the interview process for applicants with disabilities.

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