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Johnson & Johnson

Makes prescription drugs and medical devices

Manager NPI Engineering - Circulatory Restoration

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeSanta Clara, CA, USA

About the Job

Requirements

  • A B.S. in Engineering or equivalent work experience is required.
  • At least 10 years of progressive experience in medical device development, including 3 or more years leading projects across all phases of product development, is required.
  • At least 2 years managing direct reports or equivalent experience is required.
  • Knowledge of Quality System Regulation (QSR) and applicable Quality System Standards is required.
  • Experience with disposable medical device development is required; experience with coronary and/or vascular catheters is preferred.
  • A strong understanding of engineering materials, component selection, and design for safety, reliability, and manufacturability is required.
  • Experience taking a product from concept through clinical or commercial release is required.
  • Ability to work in a fast-paced environment while managing multiple priorities is required.
  • Ability to work as part of a team and/or independently while adapting to changing requirements is required.
  • The employee may be required to lift objects up to 25 pounds.

Responsibilities

  • Manage, lead, and mentor engineers and/or technicians.
  • Lead cross-functional project activities from concept through clinical trial and commercial product release.
  • Mentor and support development and engineering activities, primarily focused on catheter design and development.
  • Design and develop products and processes in compliance with company Design Control requirements and FDA, ISO, and MDD requirements.
  • Coordinate technical personnel and their activities in developing new and improved products and manufacturing processes.
  • Ensure development activities are documented in lab notebooks, history files, engineering reports, and other records.
  • Coordinate cross-functional alignment and support for program success.
  • Manage outside vendors and contractors providing products or services.
  • Create, maintain, and communicate project timelines for internal and external development projects.
  • Provide regular updates on key milestones and issues to project teams and management.
  • Identify issues and recommend solutions for products in development.
  • Contribute ideas to new product development through product specifications, process development, and manufacturing technologies.
  • Approve test methods, acceptance criteria, and test equipment for all stages of product development.
  • Review and approve documents as specified in the Document Control SOP.
  • Compile the Design History File and conduct design reviews in compliance with design control procedures.
  • Ensure products have capable manufacturing processes and that process verifications and validations are completed.
  • Work with cross-functional groups to ensure products and processes are compatible with other products and processes in the intended operating system and meet design control requirements.
  • Provide technical leadership for projects, including managing process and technology development teams.
  • Maintain current knowledge of competitive technologies and biomedical developments relevant to company products.
  • Ensure products and processes meet acceptable quality standards and customer needs in alignment with cross-functional groups.
  • Support company goals, policies, procedures, quality systems, and compliance with FDA and other regulatory bodies.
  • Perform other duties as assigned.

Desired Qualifications

  • Preferred skills include agile decision making, benchmarking, crisis management, developing others, disruptive innovations, emerging technologies, inclusive leadership, leadership, lean supply chain management, process control, process engineering, process improvements, product costing, program management, project scheduling, applying science, technology, engineering, and mathematics (STEM), team management, technical research, and technical support.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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