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Johnson & Johnson

Makes prescription drugs and medical devices

NPI Engineer 2

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

About the Job

Requirements

  • A bachelor's degree in Mechanical Engineering or Biomedical Engineering is required.
  • At least 3 years of experience in a medical device environment is required.
  • Knowledge of and compliance with applicable Quality System requirements, including QSRs, FDA, ISO, MDD, MDR, and other applicable regulations, is required.
  • Understanding of Lean and Six Sigma concepts is required.
  • Experience with medical device validation, including IQ-OQ-PQ, is required.
  • The ability to create and maintain drawings in SolidWorks is required.
  • Experience with ERP and MES is required; Oracle is preferred.
  • Basic understanding of statistics, including Cpk, hypothesis testing, design of experiments, and Gage R&R, is a plus.
  • Effective communication skills with all levels of management and organizations are required.
  • The ability to manage multiple priorities in a fast-paced environment is required.
  • The ability to work independently and as part of a team, with flexibility as requirements change, is required.
  • The employee may be required to lift objects weighing 25 pounds or more.
  • The employee will be required to work in an air-conditioned Class 8 cleanroom.

Responsibilities

  • Collaborate with Production to provide sustaining support and resolve product, process, and equipment problems.
  • Identify and participate in process, product, tooling, equipment, fixture, and cost-reduction improvement projects.
  • Coordinate or perform functional and destructive testing to support engineering reports, document results, and provide statistical analysis using Minitab or Excel.
  • Participate as an extended team member in new product introduction, including scaling up, stabilizing, and transferring products to alternate sites.
  • Participate in developing and maintaining process FMEAs, Manufacturing Process Instructions, and Device Master Record documents.
  • Create, maintain, and transfer paper Bills of Materials and Lot History Records into Item Structures, Work Definitions, and electronic Lot History Records.
  • Support resolution of Quality-related events, including NCRs, CAPAs, and audit findings, and maintain other Quality System Requirements.
  • Create and release label files for printing product labels.
  • Create and execute process validation protocols and reports.
  • Develop, validate, and implement processes with research and development, operations, regulatory, and quality teams.
  • Provide oversight to pilot manufacturing and testing, and support products transitioning from development into full production.
  • Sustain production-line activities involving raw materials, processes, and equipment.

Desired Qualifications

  • Knowledge of disposable peripheral and coronary device design, material selection, and testing is preferred.
  • Experience in early-stage catheter-based cardiovascular device projects is a strong plus.
  • Preferred skills include bioinformatics, biological engineering, biological sciences, biostatistics, data reporting, data fluency, design of experiments, detail orientation, execution focus, feasibility studies, preclinical research, problem solving, process orientation, prototyping, report writing, research and development, research, SAP Product Lifecycle Management, and technological fluency.

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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