Johnson & Johnson is currently recruiting for an Analyst II to support medical device post market surveillance processes. As the Post Market Surveillance Analyst II, you will be responsible for executing post market surveillance processes for Johnson & Johnson Medical Device companies (Acclarent, Biosense Webster, Mentor, Sterilmed, Ethicon Inc., Ethicon Endo, Neuwave, Torax, Megadyne, Depuy Synthes, Cerenovus etc.) which may span across multiple product platforms such as ENT, Neurovascular care, Device Sterilization, Electrophysiology, Surgical Aesthetics, Endoscopic Surgery, Wound Closure, Orthopedics etc.Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.Johnson & Johnson Medical Device Companies produce a broad range of innovative products and solutions used primarily by health care professionals in the fields of Johnson & Johnson Medical Devices contains key surgical platforms such as Wound Closure, Orthopedics, Open and Minimally Invasive Stapling, Energy, Biosurgery, Aesthetics, ENT, and Cardiovascular surgical products. As the most comprehensive devices business in the world, Johnson & Johnson Medical Devices is best suited to serve evolving customer needs, train more surgeons to improve standards of care, and treat more patients globally as access expands. Johnson & Johnson Medical Devices is currently $20 billion in World Wide sales. The business is expected to experience solid growth over the next 5 to 7 years.As the Post Market Surveillance Analyst II, you will collaborate with a team of engineers, data analysts and clinicians to support routine and ad hoc post market surveillance processes (e.g. complaint trending, quality system documentation, corrective action, signal detection, audit, documentation, analytics etc.). This position is considered highly visible throughout the organization due to the type of data being analyzed and presented.As an Analyst II, Post Market Surveillance, you will be responsible for:Executing post market surveillance signal detection and complaint trending processes in a highly regulated quality system environment.Compiling and executing the presentation and summary of post market surveillance statistical signals and trends.Managing cross-functional and multi-level partners to address post market surveillance requirements in a fast-paced and dynamic environment (e.g. Health authority requests, internal/external audits, field actions, CAPA, complaint handling, nonconformance, medical safety inquiries, manufacturing, statistical analysis, document control etc.).Working individually or collaborating with other Post Market Surveillance team members for continuous process improvements to challenge the status quo of the post market surveillance processes (e.g. medical device/procedure customization, documentation processes, metrics, statistical modeling, data analytics automation etc.).You Will Interface And Analyze Large Datasets Which IncludeProduct complaintsProduct malfunctionsAdverse eventsCapital equipment service recordsClinical ReviewsCompany-sponsored funded registriesExternal registries and databasesPost Market StudiesLiterature ReviewsQualificationsA minimum of a Bachelor of Science degree in a technical or clinical field (e.g. Epidemiology, Biomedical Engineering, Biostatistics, Life Sciences, Nursing, Chemistry, Quality Engineering, Health Informatics, Health Care etc.) is required.A minimum of 2 years of relevant work experience is required.Quality System and Medical Device experience is preferred.Professional or didactic application of Microsoft Office software (e.g. Outlook, Word, PowerPoint, Excel, OneNote) is required.Basic understanding of statistical analysis and ability to analyze and summarize data for presentations (e.g. Excel datasets, graphs, charts) is required.Strong written communication skills (e.g. Ability presenting well-written reports, PowerPoint presentations, facilitating discussion and navigating difficult conversations etc.) is required.Familiarity with medical procedures and terminology is preferred.The capacity to manage multiple priorities is required. The ability to work with general or limited supervision, self-learn, and self-seek solutions is preferred.Up to 10% travel for this role may be required.This position may be located in Irvine, CA; Cincinnati, OH; Somerville, NJ; West Chester, PA; or Raynham, MA.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.Primary LocationUnited States-California-Irvine-Other LocationsNorth America-United States-New Jersey-Somerville, North America-United States-Ohio-Cincinnati, North America-United States-Pennsylvania-West Chester, North America-United States-Massachusetts-RaynhamOrganizationDepuy Orthopaedics. Inc. (6029)Job FunctionQuality AssuranceRequisition ID585####### Associated topics: alarm, canine detection, loss prevention, patrol, protect, public safety, public safety officer, safety officer, surveillance, unarmed
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