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Johnson & Johnson Medtech is recruiting for a UX Designer.
This position is located in Santa Clara, California.
At Johnson & Johnson Medtech, we're changing the trajectory of health for humanity, using robotics to enhance healthcare providers' abilities and improve patients' diagnoses, treatments, and recovery times.
Johnson & Johnson Robotics was established in 2020 with the integration of Auris Health, Verb Surgical, C-SATS, and Ethicon.
It comprises three key med-tech platforms: Flexible Robotics (MONARCH™), Surgical Robotics (OTTAVA™), and Digital Solutions.
Join our collaborative, rapidly growing teams in the San Francisco Bay Area (Redwood City and Santa Clara) and Cincinnati.
You'll collaborate on breakthrough medical technologies that unite multiple subject areas to build a connected digital ecosystem that advances medical professionals' skills and improves patient outcomes.
Overview
You will join the Human Factors & Experience Design (HFXD) team and implement the UX strategy on the OTTAVA™ surgical robotic system and related experiences.
Working closely with designers, product management and human factors, you will drive the future of surgical robotics.
Your day to day will incorporate learning about life-changing surgical procedures, creating designs that progress the robotic roadmap, and crafting the best user experience for the entire medical team.
Surgery is a team sport, so you will be encouraged to become familiar with a range of user types across a variety of clinical specialties.
You'll bring your passion for design to a broad range of projects using both internal and external resources.
As a member of the HFXD team reporting to the UX Design Manager, you'll join a team culture that is inclusive, creative and obsessed with improving experiences for our users.
We strive to build impactful work while also crafting a positive environment for us all to work in.
Does this sound like an opportunity that fits your skills and ambition? If so, we encourage you to apply below!
Responsibilities
* Work within a team of UX designers to produce concepts and UX designs for the OTTAVA surgical robot
* Work with Industrial Designers, Human Factors Engineers, and User Experience Researchers to promote a unified vision of the User's best experience
* Collaborate with teams and partners to dissect requirements and agree on the best features and functionality for the surgical team
* Partner with the rest of HFXD to craft the team culture and advance the team's overall impact across experiences that we support
Education:
* Bachelor's or equivalent experience in Human-Computer Interaction, Digital/Visual Design, Industrial Design or other related field
Experience and Skills:
Required:
* At least 2 years of experience designing for complex and sophisticated systems
* Proficiency with typical UX design and prototyping tools (Adobe Suite, Figma, Principal, etc.)
* Strong portfolio demonstrating an ...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:17
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Medical Device Business Services, Inc.
and Synthes GmbH, a member of the Johnson & Johnson Family of Companies, is recruiting for a Director, NPI and LCM - HKP/AH/Ex-Fix, ( H ip/Knees/Pelvis, Animal Health, and External Fixation) to be located in Zuchwil, Switzerland or West Chester, Pennsylvania.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Reporting to the Sr.
Director, NPI and LCM - TECA & Sports, the Director, NPI ad LCM - HKP/AH/Ex-Fix is expected to lead the engineering Supply Chain performance to contemporary, standard methodology manufacturing and supply chain processes and techniques on a global scale, including the integration of acquired entities.
This leader is has responsibility for overall End to End (E2E) supply chain engineering performance for products within the Hip-Knees-Pelvis (HKP) / Animal Health (AH) / External Fixation (Ex-Fix) value stream, including supporting new product development, lifecycle management to end of life, including launch management of new products from the supply chain function, process improvements, projects, capital management, cost improvements, and developing strategies for innovation and manufacturing of the future.
This leader will have a strong combination of strategic vision and a willingness to be hands-on in all aspects of new product introductions, technical transfers, global manufacturing, and supply chain operations as appropriate.
The Director, NPI ad LCM - HKP/AH/Ex-Fix will have global Supply Chain leadership responsibility of $2.1B across all global external manufacturing sites, more than 25,000 SKUs, annual COGS of ~$450MM with total annual cost actions of $12MM .
The Director, NPI ad LCM - HKP/AH/Ex-Fix will partner closely with Jabil Healthcare, the TECA strategic external manufacturing collaborator, and other external manufacturers to implement new product launches and ensure timely execution of LCM projects in the areas of patient safety, compliance, quality, service, and value capture for their product portfolio.
The Director, NPI ad LCM - HKP/AH/Ex-Fix will be a member of the HKP/AH/Ex-Fix Value Stream Team and will be instrumental in developing supply chain strategies as a part of Product Strategy Roadmaps and Mission Critical teams which will enhance supply chain reliability, agility, resilience, and product profitability.
They will work closely with other functions, including R&D, Quality, Regulatory Affairs, External Manufacturing, and Commercial.
KEY RESPONSIBILITIES:
• Has responsibility for ...
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Type: Permanent Location: West Chester, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:16
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Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Technical Documentation Specialist located in Danvers, MA.
This role is open to remote work.
Abiomed, part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives.
Abiomed's "Patients First!" culture drives our skilled workforce and strong relationships with clinicians.
Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.
Founded in 1981, Abiomed has a proven track record for growth, integrity and innovation.
Th is position will work closely with the Manager of Promotional and Educational Compliance as well as content creators across the enterprise .
Assist in Global company growth by providing documentation that serve s our customers and meet local, federal and international regulations and guidance.
This person will prepare instruction manuals, and other supporting documents that communicate complex and technical information to customers.
This position has overall responsibility for managing the content, structure and consistency of Abiomed's instructions for product use documents.
Th is position works with Regulatory, Advanced Clinical Training & Support, Product Management, Engineering, Marketing , and compliance .
K ey components of the position include :
* Ensures that all Instructions for Use (IFUs), are up to date and consistent with current product iteration, procedure and technique, and software version.
* Manages delivery of all final content, in multiple formats, and ensures its appropriately routed for approvals
* Ensure these customer facing documents are stored and distributed to all required locations in accordance to SOP-QA27
* Manage the translation process for these key and complex documents and ensure all images and terms in these documents are accurately represented in all training materials created from them.
* Ensure all documents comply with federal, state and industry regulations and standards as well as company branding and messaging.
* Copy e diting for grammar, punctuation, consistency, clarity, and style as defined by the company guidelines
* This job is centered around fact-checking and the oversight of medical and scientific materials.
As well as fulfilling the need for a central location to our product specifications, per software and country.
* Assist in manag ing product Claims matrixes and Clinical Publication Library for promotional and educational purposes
* Use Veeva Vault PromoMats to track and communicate these Claims to all Abiomed promotional and training material content creators
* Exercise excellent service standards and maintain high customer satisfaction through resolving problems by explaining the best solution, expediting correction or adjustments t...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:15
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DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world.
DePuy Synthes Companies offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials.
Building on the legacy and strengths of two great companies, we are creating one organization that will be agile and better equipped in today's evolving health care environment.
With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.
DePuy Synthes Power Tools offers a comprehensive range of air, electric, and battery-driven high and low power instrument systems, including drills, reamers and saws.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
DePuy Synthes, a member of the Johnson & Johnson Family of Companies, is currently recruiting a Supply Chain Business Analyst (50%) to join its team.
Zug, Switzerland is the preferred primary location.
Initial contract duration is for 12 month with a possibility of extension.
What you will be doing:
Supply Chain Business Analyst supports on daily activities on current Supply Chain processes and advanced Business Analytics tools.
Helps implement processes, documentation and training material in support of the organization's overall Supply Chain strategy and Business Intelligence (BI) area, under close supervision.
In your day-to-day job you will:
* Support on development and documentation of a comprehensive analytics platform roadmap and strategy.
* Does simple trend analysis to support continuous improvement efforts for the organization's BI strategy.
* Runs data entry and data consolidation processes to support the analysis and assessment of existing dashboards.
* Update datasets and data inputs user documentation files for Alteryx flows and Power BI tools
* Supports on training material and process documentation for existing Alteryx flows and Power BI dashboards
* Contributes to less complex components of projects, programs, or processes for the BI area.
* Collaborate with Supply Chain Planning team on gathering feedback about solutions that improve visualizations and existing Analytics tools
* Support with the daily activities and ad-hoc tasks
* Understands and applies Johnson & ...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:14
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Johnson & Johnson MedTech is recruiting for a Senior Human Factors Engineer, located in Santa Clara, CA.
At Johnson & Johnson MedTech, we're changing the trajectory of health for humanity, using robotics to enhance healthcare providers' abilities and improve patients' diagnoses, treatments, and recovery times.
Johnson & Johnson Robotics was established in 2020 with the integration of Auris Health, Verb Surgical, C-SATS, and Ethicon.
It comprises three key med-tech platforms: Flexible Robotics (MONARCH™), Surgical Robotics (OTTAVA™), and Digital Solutions.
Join our collaborative, rapidly growing teams in the San Francisco Bay Area (Redwood City and Santa Clara), Cincinnati, and Seattle.
You'll collaborate on breakthrough medical technologies that unite multiple subject areas to build a connected digital ecosystem that advances medical professionals' skills and improves patient outcomes.
Overview
You will join the Human Factors & Experience Design (HFXD) team and help shape OTTAVA™, Johnson & Johnson's new surgical robotic system.
As a Senior Human Factors Engineer on the team, you will be responsible for running Human Factors workstreams as the primary individual contributor.
You will work in close partnership with cross-functional colleagues to meet program objectives, using your disciplinary expertise and passion for safety and usability to influence key design decisions.
You will be encouraged to act with autonomy as a trusted expert, while being able to rely on the support of your team and leadership to support you when needed.
Our collaborative culture heavily emphasizes growth and development and you'll help mentor and develop HF talent on the team, while also receiving mentorship to help you grow in your career.
Does the idea of working in medical robotics excite you? Are you a seasoned professional who is motivated by impacting patients globally with your work? If so, we'd love to hear from you!
Responsibilities:
* Lead complex human factors work, using best-in-class methodologies to inform rigorous decision-making
* Support product submissions and collaborate with regulatory bodies
* Act as a knowledgable contributor on human factors methodologies
* Apply knowledge of FDA, ISO, AAMI and other relevant regulations and standards
* Provide some guidance to Human Factors engineers
Education
Required
* BS/BA Degree in Human Factors Engineering (HFE), Cognitive Science, Psychology, Industrial Engineering, or equivalent is required.
Preferred
* Post-Graduate Degrees (MS, PhD) are a plus and will be considered as part of the applicant's professional experience.
Experience and Skills:
Required
* Minimum Human Factors engineering experience: Bachelor's plus 5 years, Master's plus 2 years, PhD with no additional years required.
* Experience in the planning and execution of aspects of the HFE process under the constraints of Design Controls.
* Hands-on experience partnering with R...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:14
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About Johnson & Johnson
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Johnson and Johnson is recruiting for an Abiomed Surgical Account Manager located in Poland
Contract: Full time
Surgical Account Manager develops our surgical business and ensure best clinical outcomes.
Our goal is to establish Heart Recovery as new standard of Care which requires a Heart Team approach.
Key Responsibilities:
• Identify opportunities, generate market awareness, and drive adoption of Abiomed's surgical product portfolio.
• Open new accounts and built KOL's
• Educating customers regarding the indications, contra-indications, and technical applications of Abiomed's product portfolio.
• Support surgical cases if appropriate
• Manage the transition from the initial purchase to the clinical implementation of the product to drive adoption.
• Work collaboratively with the surgical clinical consultant and the cardiology team in the assigned region to achieve quarter over quarter growth.
• Drive excitement and vision of heart recovery solutions with existing devices and the future technologies.
• Organize and execute surgical round tables (PPD)
• Call point(s): Cardiac Surgeons, HF Surgeons, HF cardiologists, Intensivists, ICU nurses & Perfusionists
• Organize HEART Team approach with local TM/CS colleague
• Staff major conferences & local heart failure symposiums.
• Build surgical vertical in established Impella programs - Full product portfolio.
• Demonstrate a strong work ethic and represent the company with high integrity, ethics, honesty, loyalty, and professionalism.
• Conferences: Represent us at surgical conferences across the EMEA region.
• Ability to travel 80% within territory required.
Qualifications :
• Educational Skills: Bachelor's degree
• 5 years' experience of cardiac surgery and/- or surgical medical device sales in the field of Heart Failure and MCS business
• strategic selling skills,
• Strong knowledge of cardiac surgery, perfusion medicine, mechanical circulatory support, structural heart anatomy,
• Direct patient support experience
• Fluency in English and Polish
In return, we offer:
* An opportunity to be part of a global market leader.
* A dynamic and encouraging working environment, at a regional and global level.
* Possibilities for further personal as well and professional development.
* A competitive salary and bonus.
* An extensive list of benefits including a health insurance...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:13
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At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity.
Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Next Move Could Mean Our Next Breakthrough.
We are hiring the best talent for Trilingual Customer Service (Portuguese English & Spanish) to be located in Bogotá,Colombia (Relocation not applicable)
Purpose"
The Global Services Advocate Trilingual Customer Service (Portuguese English & Spanish) will work to resolve global client inquiries, concerns and issues on one of our identified functions through our multiple channels including phone, fax, email, web-form, and chat.
This person works to meet all expected service levels and business performance goals, performing a full range of services and fully documenting all cases in the Case Management system.
This person supports J&J employees and the GS community regarding all inquiries related to HR Services, employee programs and services, process, and procedures including navigational support working with the Contact Center on escalations.
Key Responsibilities:
* Receive inbound inquiries via multiple channels (phone, email, fax, web-form, chat), clarify the need, answer the inquiries and assist in the resolution of concerns.
* Access enabling technology to complete client inquiries and transactions.
* Fully document all cases in case management application.
* Escalate complex transactions for resolution or contact with third party vendors as appropriate.
* Attend to and process customer inquiries and request by applying Global Contact standard operating procedures and utilizing problem solving skills for resolution.
* Assist and encourage users / customers to make effective use of self-service options, systems, products, services, etc.
in order to drive rapid resolution and empower customers; educate and inform customers of the full range of Global Services available to them.
Education: High School required or Bachelor's degree (preferred)
REQUIRED:
* Customer service experience
* Proficient in these 2 languages: Spanish (advanced required), English (advanced required).
* Demonstrates customer orientation and !excellent customer service skills!.
* Strong written and verbal communication skills; handles internal communications and external/client communications with detailed support and assistance
* Excellent telephone manner with clear, concise and professional communication skills
PREFERRED
* Experience with tools to report data, track and analyze trends...
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Type: Permanent Location: Bogotá, CO-DC
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:12
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Johnson & Johnson's Innovative Medicine is recruiting for a Director of Oncology Data Science.
You will report to the Head of Hematology & Oncology Data Science.
The primary location for this position is either Titusville, NJ, New Brunswick, NJ or Spring House, PA.
Consideration will be given to Boston, MA, Raritan, NJ, La Jolla, CA or other JRD locations.
Who we Are: J&J Innovative Medicine develops treatments that improve the health and lifestyles of people worldwide.
Research and Development areas encompass Oncology, Cardiovascular and Metabolic disorders, Immunology, Neuroscience, and Infectious diseases.
Our ultimate goal is to help people live longer, healthier lives.
We have produced and marketed many first-in-class prescription medications and are poised to serve the broad needs of the healthcare market - from patients to practitioners and from clinics to hospitals.
To learn more about J J&J Innovative Medicine, one of the Pharmaceutical Companies of Johnson & Johnson, visit https://www.janssen.com/johnson-johnson-innovative-medicine .
You will:
Position summary:
* Serve as primary business leader for Data Science & Digital Health for Early Development programs for robust Hematology Oncology portfolio.
* Serve a bifunctional role as a Data Science translator and a Early development Leader/ Data Science liaison to the Oncology Therapeutic Area
* Work closely with individual clinical teams as well as functional area partners (e.g., Translational research, Precision Medicine and diagnostics, Regulatory Affairs, Market Access, Clinical Development) to identify and implement end-to-end Data Science solutions aimed at facilitating decision making.
(e.g.
study design, execution, diagnostic planning and strategy)
* Orchestrate and drive solutions with matrixed teams, including technical Data Science teams (e.g.
RWD, AI/ML).
This will include the evaluation and development of external partnerships that can leverage new technologies/solutions for clinical trials.
* Provide leadership for Oncology Data Science & Digital Health on investments, strategy and future business planning.
* MD with clinical experience (e.g., residency), Ph.D., Masters or Bachelors degree in Medicine, Biotechnology, Statistics, Machine Learning & Artificial Intelligence, Physics, Mathematics, Computational Chemistry, Computational Biology, Biology or a related discipline.
* A minimum of 5 years industry experience in drug development or related discipline in the field of biotechnology.
* Strong working knowledge of drug development, with established expertise with multiple components of drug development, such as translational research, clinical studies, or regulatory interactions.
* Familiarity with healthcare relevant datasets, such as EHR, insurance claims or registry data.
* Established leadership skills, including management of individuals and teams working towards common clinical/scientific goals
* Consistent ...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:11
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Abiomed ist ein innovatives Medizintechnik-Unternehmen mit einer inspirierenden Mission "Patients First." und einem einzigartigen Firmenmotto "Herzen regenerieren.
Leben retten".
Mit mehr als 3.000 Mitarbeitern ist Abiomed eines der am schnellsten wachsenden Medizintechnik-Unternehmen weltweit mit dem Firmenhauptsitz in Danvers, USA sowie Standorte in Aachen und Berlin, Deutschland, Tokio, Japan und Singapur.
Abiomed ist Teil von Johnson & Johnson MedTech.
Abiomed ist ein Arbeitgeber mit attraktiven Arbeitsbedingungen und einer wertschätzenden Unternehmenskultur, bei dem die Bedürfnisse der Mitarbeiter im Fokus stehen.
Abiomed begeistert und bindet außerordentliche Talente durch Zusammenarbeit, Leidenschaft und kontinuierliche Weiterentwicklung.
Wir suchen aktuell einen Regional Clinical Educator / Clinical Consultant (m/w/d), für die Region Westdeutschland.
Spannende Aufgaben warten auf Sie:
• Patientenbetreuung: Verbesserung der Patientenergebnisse durch eine fachgerechte Ausbildung und Beratung des medizinischen Personals.
• Betreuung aller Kliniken, in denen Patienten mit Impella® Produkten behandelt werden.
• Reportings von klinisch relevanten Daten, Dokumentation von Ergebnissen und eine enge Zusammenarbeit mit unseren Teammitgliedern und Vertriebskollegen.
• Klinische Beratung: Durchführung von Trainings zur Steigerung der klinischen Auslastung und Leistung unserer Kunden.
Verwaltung von Schulungen für unsere neuen und bestehenden Kunden.
• Training/klinische Demos: Unterstützung bei der Koordination von klinischen Demos vor Ort.
Ihr Profil:
* Erfolgreich abgeschlossene klinische oder klinisch-technische Ausbildung, idealerweise als Gesundheits- bzw.
Krankenpfleger(in) oder Kardiotechniker(in) / Klinischer Perfusionist(in).
* Mehrjährige Berufserfahrung in der direkten Patientenbetreuung auf Intensiv- oder Pflegestation, im OP oder im HKL.
* Überzeugendes Auftreten und die Fähigkeit, langfristige Kundenbeziehungen weiterzuentwickeln und zu fördern.
* Gute Kommunikations- und Präsentationsfähigkeiten sowie Teamfähigkeit.
* Hohe Flexibilität und 80% Reisebereitschaft innerhalb der vorgegebenen Regionen sowie Einsatzbereitschaft für Notfallsituationen.
Wir bieten:
* Angenehme, offene Unternehmenskultur mit einer starken Mission: "Recovering Hearts, Saving Lives" und dem Fokus auf Mitarbeiterentwicklung
* Innovative Produkte und Technologien mit Fokus auf die native Herzerholung am Markt zu etablieren und damit den Standard in diesem Bereich zu revolutionieren
* Attraktives Gehalt sowie einen Firmenwagen mit privater Nutzung
* Zuschuss zur betrieblichen Altersvorsorge von bis zu 1.500, - Euro im Jahr und vermögenswirksame Leistungen
* Vorteilspakete für eine Berufsunfähigkeitsversicherung und eine betriebliche Gruppenunfallversicherung
* Diverse Gesundheitsprogramme und Leasingmöglichkeit für ein Job-Rad
ABIOMED ist ein Arbeitgeber, der Chance...
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Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:10
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Johnson & Johnson is currently recruiting for a Process Engineer II!
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Are you interested in making a difference in a thriving diverse company culture, that celebrates the uniqueness of our employees and is committed to inclusion Apply today!
JOB SUMMARY
*
This role provides engineering support for manufacturing operations based within the value streams.
The role requires technical ownership to be taken for manufacturing processes, products, and equipment, while maintaining a focus on key business drivers, which include EH&S, Quality, Supply and Cost.
This role provides process engineering and controls support.
Plans and conducts activities related to the development of new processes including researching current and emerging technologies, evaluating process cost, quality, and capability alternatives, and performing process characterization and optimization using designed experiments, and problem solving and decision-making tools.
As process owner, this role will involve collaborating with a number of functional groups delivering value stream projects, such as NPI and Manufacturing Engineering, as well as with suppliers and other sites within the engineering, science, and technology network that run similar processes.
This position will foster opportunities, strong leadership, work ethic, and Credo-based behaviors.
DUTIES & RESPONSIBILITIES
*
Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
o Participates in comprehensive engineering activities to develop and implement effective, high-quality processes and design guidelines for dissemination throughout the division.
o Provides moderately complex design reviews and feedback for improvements in manufacturability.
o Implements equipment, materials, and process performance requirements, performs vendor searches and equipment evaluation to ensure adequate capability to produce quality products in required quantities at an effective cost.
o Facilitates experiments and capability studies, develops process specifications, and designs and procures process tools.
o Evaluates and advises on the selection of suitable equipment for optimized, balanced line performance.
o Processes analyses of new systems and equipment with the intent of achieving continuous improvement of present methods.
o Edits and publishes process documentation and training materi...
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Type: Permanent Location: Warsaw, US-IN
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:09
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Auris Health Inc., a member of the Johnson & Johnson Family of Companies, is recruiting for a Manager, Service Repair Center.
This position is based in Santa Clara, CA.
About Johnson & Johnson
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Ethicon is a technology company defining the future of medical intervention.
By combining advancements in medical robotics, instrumentation, navigation and data science, Ethicon is building a platform technology capable of expanding the applicability of robotics to a spectrum of medical procedures.
The Flexible Robotics Service Repair Center team is seeking a Service Repair Center Manager to lead daily operations, perform planning, analysis of service inventory consumption and the replenishment levels required to maintain on-hand availability of service Field replaceable units (FRUs) as needed.
Overview
Directs the Service Repair Center through collaboration with planners and schedulers.
Identifies requirements for the business to improve planning efficiency and materials management.
Establishes priorities and sequences for rework, repair, refurbishment, and disposal of service consumed Field Replaceable Units (FRU's).
Responsible for supplying product(s) and service spares to the field services team and driving service inventory to sustainable min/max levels.
Approves and develops mechanisms to resolve service inventory related issues.
Alters refurbishment work order schedules to meet unforeseen conditions.
Builds business partnerships with inventory management teams, shipping, purchasing and suppliers to effectively support the refurbishment, rework, and repair of FRU's.
Establishes key performance indicators (KPIs) and metrics to improve profitability through reduction in new parts shipments and increased utilization of refurbished, reworked parts, and utilization of resources.
Evaluates issues and meets with service and supplier management as needed to ensure steady supply of materials for field service use and to evaluate Service Level Agreement (SLA) performance.
Participates in making business decisions on new product launches that require Service Repair Center support to develop stocking levels and service FRU forecasts.
Key Responsibilities
* Lead the day-to-day Flexible Robotics Service Repair Center operation, administration, and repair center engineering team.
* Manage the creation, process management, closure and transfer of materials utilizing established ERP and CRM systems in conjunction with materials man...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:09
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Johnson and Johnson, is recruiting for an Integrated Evidence Team Leader (IETL), Dermatology- Director for the US Immunology Medical Affairs organization located in Horsham, PA.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
The Director, Integrated Evidence Team Leader (IETL), Dermatology Therapeutic Area (TA) is responsible for understanding the US healthcare environment and the various stakeholders relevant to the success of the overall Immunology therapeutic area, with focus on Dermatology.
This position will report to the Senior Director, Dermatology Therapeutic Area Leader (TAL), Medical Affairs.
The Director, IETL, Dermatology leads a cross-functional partner team to identify opportunities and gaps in the evidence and knowledge needed to drive stakeholder-focused value propositions, prioritize and integrate evidence generation activities from across research/data groups (e.g., Medical Affairs, HECOR/V&E, RWE, epidemiology, market research, etc.) to ensure success of the Dermatology TA.
In this role you will:
• Work collaboratively within the Dermatology TA team (medical directors, medical communications and scientific exchange, field MSLs, value and evidence, etc.), as well as across key partner organizations (including but not limited to US and Global commercial, global medical affairs, research & development, US and global market access, etc.).
• Lead the cross-functional Dermatology IET to develop and maintain a strategically aligned integrated evidence generation plan (IEGP) in support of both in-line and pipeline assets.
• Lead the development of a strategically aligned communication and dissemination strategy, and work with appropriate cross-functional partners to maintain and execute an integrated data dissemination plan across medical, commercial, consumer, and payer communication channels.
Key Responsibilities:
• Work with the Dermatology TAL to lead the development of the overall strategic direction of the Dermatology TA and ensure broad alignment with the Rheumatology TA as well as the overall Immunology portfolio strategy.
• In partnership with cross-functional area team leaders, develop and drive IEGP initiatives to meet the evolving needs of key internal and external stakeholders (medical, commercial, payer):
-Drive decision-making on the US integrated evidence generation and dissemination strategy, ensuring relevant research, analysis, competitive data, and expertise are considered.
Contribute relevant US insights to inform, influence,...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:08
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At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Job Purpose:
Reporting to the Senior EH&S Compliance Specialist the EH&S Compliance Specialist will a ssist with the design, implementation, maintenance and review of Environmental and Sustainability programmes to ensure compliance with regulatory, corporate and industry requirements.
We in EH&S act as advisors to all teams on site in relation to EH&S matters.
Key Responsibilities:
* Assist with the design, implementation, maintenance, and review of the company's Environmental Health & Safety (EH&S) and Sustainability programmes to ensure compliance with legislative, corporate and industry requirements and support the achievement of ISO14001 & ISO45001.
* Assist in the management of all environmental related matters including, Waste, Industrial Emissions (IED) Licence, Green House Gas (GHG) Permit and Genetically Modified Organism (GMO) Permit.
* Assist with the preparation of EHS reports as required for both internal and external groups e.g.
J&J Corporate reporting requirements, EPA annual reporting for both IE Licence and GHG Permit.
* Provide Environmental Compliance support to operations on site and for site projects through Concept, Design & Operation.
* Provide support to site Sustainability resources and initiatives.
* Provide support for EH&S Incident investigation.
Support root cause analysis and reporting
* Conduct EHS Impact Assessments (IA) to ensure that all EH&S or sustainability requirements and J&J standards are in place.
* Perform periodic walkdowns / audits / programme reviews to ensure compliance with environmental permits, plans, policies, and regulatory requirements.
* Ensure there are effective EH&S Compliance communication & training program for EH&S activities in addition to updating policies and procedures as/when required.
* Provide proactive EH&S support and mentorship to functions and business units, providing clear understanding of Environmental EH&S standards, legislative requirements and site procedures.
* Support development and improvement of EH&S compliance training and performance
* Support continued evolution of site EH&S, compliance and Sustainability culture through effective communication and participation.
* Provide assistance in generation of EHS metrics and EHS management system performance tracking
* Perform to high standards at all times in compliance with Credo and EH&S Standards.
Additional scope -
* Assis...
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Type: Permanent Location: Cork, IE-CO
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:07
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Johnson and Johnson is recruiting for a Medical Director, Dermatology Therapeutic Area for the US Immunology Medical Affairs organization located in Horsham, PA.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
As a part of Medical Affairs Immunology, the Medical Director, Dermatology Medical Affairs, will contribute to the strategic planning and execution of Phase 3b/4 trials, post-marketing requirement studies, investigator initiated or collaborative studies.
The Medical Director, Dermatology Medical Affairs will contribute/ lead the advancement of protocol development, medical/ data monitoring, study operations, data analysis/ reporting, writing of study reports and publications, as applicable.
In addition, the Medical Director, Dermatology Medical Affairs will partner with colleagues in real-world evidence, health economic and outcomes research, biostatistics, commercial, and field (medical/ commercial/ value and evidence) based teams through integrated evidence teams and other touchpoints to formulate and execute activities in support of the Dermatology TA strategy on marketed and/or pipeline products, as well as supporting the fulfillment of medical information questions and issues that arise from the medical or commercial field teams and internal/external customers in the Dermatology TA.
In this role you will:
• Develop and execute Medical Affairs sponsored clinical programs, including but not limited to Phase 3b/4 trials, registries, real-world evidence studies, investigator-initiated and/or collaborative studies in the Dermatology TA.
Contribute/ lead study design, protocol development, clinical study report and publication development.
Work closely with the matrix clinical trial teams on study operations and provide program leadership and medical oversight.
• Provide Dermatology subject matter expertise and represent US medical affairs on internal stakeholder/ project teams across multiple functional areas including but not limited to sales and marketing, health economics and outcomes research, value and evidence, field MSLs, medical communications and scientific exchange.
• Provide US medical affairs input and US stakeholder insights to R&D clinical development programs, including clinical trial study designs, presentations, and publications.
• Support the fulfillment of medical information requests from field medical and field commercial teams.
Support/ lead the development of medical education content for field medical team.
Partner with medical commun...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:06
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Janssen Pharmaceutical, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Analyst, Quality Control - Microbiology CAR-T Manufacturing (2nd Shift) in Raritan, NJ!
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We are Janssen.
We collaborate with the world for the health of everyone in it.
Learn more at www.janssen.com and follow us @JanssenGlobal.
Janssen Biotech, Inc.
is part of the Janssen Pharmaceutical Companies.
Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy.
This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR-T platform and investigational treatment.
Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity!
The Microbiology CAR-T Manufacturing QC Analyst is responsible for collaborating with the Operations Team to conduct environmental monitoring within the manufacturing facility.
Additional responsibilities in the QC laboratory include environmental monitoring plate reads and endotoxin testing.
They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and cGMP regulations.
They typically work with a team of 5 - 15 other Associates within the functional Quality Control laboratory and the Manufacturing area.
Key Responsibilities:
* Participate in CAR-T manufacturing facility commissioning and qualification.
* Perform compressed gas sampling and Routine Environmental Monitoring of classified areas within the Raritan manufacturing facility.
* Perform endotoxin testing.
* Participate in gown qualification and requalification of personnel.
* Create, review, and approve relevant QC documents, SOPs, and WIs.
* Support Aseptic Process Simulations and visual inspection of components.
* Utilize electronic systems (eLIMS) for execution and documentation of testing.
* Perform peer data review/approval of laboratory data.
* Initiate quality investigations related to environmental monitoring.
* Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
Education:
* Minimum of a Bachelor's or equivalent degree required; focused degree in Biological Science or equivalent technical field preferred
Experience and Skills:
Required:
* Minimum two (2) years of relevant work experience
* Experi...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:05
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At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world's most significant healthcare challenges.
Our Corporate, Consumer Health, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.
We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.
With a reach of more than a billion people every day, there's no limit to the impact you can make here.
Are you ready to reimagine healthcare?
Here, your career breakthroughs will change the future of health, in all the best ways.
And you'll change, too.
You'll be inspired, and you'll inspire people across the world to change how they care for themselves and those they love.
Join us!
Johnson & Johnson innovative medicine is recruiting for a Summer Intern/Co-Op - Immunology, located in Spring House, PA.
The Immunology Discovery group is focused on discovering novel therapeutics to treat inflammatory and autoimmune diseases.
The broader group focuses on adaptive immune mechanisms and pathways, and includes members at the Spring House, PA; La Jolla, CA; and Cambridge, MA campuses.
Responsibilitie s:
* The Summer Intern/Co-Op in Immunology will actively engage in early discovery efforts to support Janssen's Immunology discovery strategy
* In intern will be resp onsible with the guidance of their mentor in the p lanning and execut ion of experiments to interrogate the biology of inflammasome responses in innate immunity.
* Experimental analysis will utilize stand immunological techniques including c ell culture with cell lines and primary human monocytes , b iochemical assays including Western Blotting, Immunoprecipitation and ELISA and c ell based assays of viability
* The candidate will be responsible for interpret data, troubleshoot issues, and effectively present the findings to the project team and senior colleagues.
* Follow all Environmental, Health & Safety laboratory safety standards and maintain company compliance requirements.
Qualifications
In order to be eligible, you must meet the following criteria:
* Legally authorized to work in the US and must not require sponsorship for employment visa status now or in the future (ex.
H1-B, F-1)
* Currently pursuing a University degree, completing minimum undergraduate sophomore year prior to internship or co-op start date.
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.
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:04
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Abiomed, Inc.
part of the Johnson & Johnson Family of Companies , is recruiting for a Part-Time Clinical Consultant located in Greensboro, NC .
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/ .
The Part-Time Clinical Consultant (PTCC) role is an exciting opportunity to join Abiomed, one of the industry's fast-growing medical device companies.
This role is the first step for Nurses, Advanced Practice Providers, and Cardiology or Radiology Techs to join our world-class field organization.
This part-time position will be responsible for providing case support, patient management, and education to both new and existing accounts within an assigned Franchise/Region.
Duties and Responsibilities:
* Acquire and demonstrate a working knowledge of our products/therapies and develop an understanding of their applications.
* Improve patient outcomes by delivering Impella® education in a variety of settings, including but not limited to, the ICU, OR, and Cath Lab.
* Impella® case support, including on-call support.
* Completing proactive rounds for patients receiving support and assistance.
* Collaborate with the Clinical Support Center (CSC) for ongoing additional support as necessary.
* Maintain clinical competency in current product line, patient management, and remain up to date on most relevant information through continual learning and education.
* Some travel may be needed.
* Clinical certification is required; a Registered Nurse (RN)/Advanced Practice Provider (APP) license is strongly preferred.
* 3 years' experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required.
CVICU experience is highly preferred.
* Some industry experience is preferred, but not required.
* Significant experience with Impella® is required (minimum of 10 cases/patients supported).
* Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of availability per month.
* Availability must include (1) weekend per month.
* Ability to work on weekends, nights, holidays as well as weekdays.
* Ability to work at other hospitals aside from base location.
The hourly rate for this role is $60/hr.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without...
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Type: Permanent Location: Greensboro, US-NC
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:04
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Abiomed, Inc.
part of the Johnson & Johnson Family of Companies , is recruiting for a Part-Time Clinical Consultant located in Hickory, NC .
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/ .
The Part-Time Clinical Consultant (PTCC) role is an exciting opportunity to join Abiomed, one of the industry's fast-growing medical device companies.
This role is the first step for Nurses, Advanced Practice Providers, and Cardiology or Radiology Techs to join our world-class field organization.
This part-time position will be responsible for providing case support, patient management, and education to both new and existing accounts within an assigned Franchise/Region.
Duties and Responsibilities:
* Acquire and demonstrate a working knowledge of our products/therapies and develop an understanding of their applications.
* Improve patient outcomes by delivering Impella® education in a variety of settings, including but not limited to, the ICU, OR, and Cath Lab.
* Impella® case support, including on-call support.
* Completing proactive rounds for patients receiving support and assistance.
* Collaborate with the Clinical Support Center (CSC) for ongoing additional support as necessary.
* Maintain clinical competency in current product line, patient management, and remain up to date on most relevant information through continual learning and education.
* Some travel may be needed.
* Clinical certification is required; a Registered Nurse (RN)/Advanced Practice Provider (APP) license is strongly preferred.
* 3 years' experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required.
CVICU experience is highly preferred.
* Some industry experience is preferred, but not required.
* Significant experience with Impella® is required (minimum of 10 cases/patients supported).
* Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of availability per month.
* Availability must include (1) weekend per month.
* Ability to work on weekends, nights, holidays as well as weekdays.
* Ability to work at other hospitals aside from base location.
The hourly rate for this role is $60/hr.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without re...
....Read more...
Type: Permanent Location: Hickory, US-NC
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:03
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Scientist
Description:
Johnson&Johnson's Innovative Medicine is recruiting for a Scientist in the Global Process, Biotherapeutic's Drug Product Development and Delivery organization, located in Schaffhausen, Switzerland.
At the Johnson & Johnson Innovative Medicine, what matters most is helping people live full and healthy lives.
We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time.
And we pursue the most promising science, wherever it might be found.
The candidate for this position will be responsible for process development and technology transfer of fill/finish manufacturing processes of biotherapeutic products.
The candidate will also work and partner with colleagues in MSAT, Quality, Regulatory, and other functions to ensure the implementation of manufacturing processes that meet all regulatory requirements and expectations.
Primary responsibilities:
* Lead late-stage process development, technology transfer, process validation, and filing activities both to and between manufacturing sites (internal/external network) by providing Scientific support as well as technical project management.
* Responsible for timely authoring of tech transfer documents (e.g.
tech transfer/process validation protocols and reports, criticality analysis and regulatory submissions).
* Partners with cross functional groups to ensure processes are consistent to accepted Janssen platforms and are in compliance with the submitted CMC dossiers and general cGMP regulations.
* Provides feedback to development teams about technical performance and consistency with the Janssen process development approach.
* Participates in parenteral networking to ensure a seamless transfer of drug product manufacturing processes from lab through pilot to commercial scale.
Qualifications:
* A technical expert on current and future manufacturing principles and processes, preferably with an application to large molecule fill and finish.
* Demonstrated competency and experience in biologics drug product development within the biopharmaceutical industry is required.
* Must have knowledge of drug substance and/or drug product process.
* Knowledge and applied experience of biopharmaceutical process design, technology transfer and drug product fill/finish operations is preferred.
* Experience with a variety of container-closure systems including vials, syringes and applicable delivery devices is preferred.
* Ability to collaborate with cross functional teams is a must.
* Excellent oral and written language skills in German and/or English.
* Motivated, self-starter able to work with a high level of autonomy with demonstrated problem-solving skills.
Degree:
Master Degree in Chemistry, Biochemical Engineering, Chemical Engineering, Pharmacy or a related field with at least 4 years of experience OR a PhD in Chemistry, Biochemical Engineering, Chemical Engineering, Pharmacy...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:02
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Senior R&D Engineer II - Sustaining & Lifecycle Management
Location: Ballybrit, Galway
Live Our Credo & Pursue Our Purpose:
As part of the Johnson & Johnson family of companies, Our Purpose is 'We blend heart, science and ingenuity to profoundly change the trajectory of health for humanity.' We are guided by the values in Our Credo.
With responsibility to patients, employees, communities, and stakeholders, Our Credo puts the needs of each of those first.
Diversity, Equity & Inclusion:
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences
That is why we in Ireland are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential.
No matter who they are.
Diversity, Equity & Inclusion at Johnson & Johnson means "You Belong".
Cerenovus:
CERENOVUS, part of Johnson & Johnson Medical Devices Companies, is a global leader in neurovascular care.
Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship.
CERENOVUS offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.
What is it like to work at CERENOVUS Galway?
* Culturally, we are putting the needs of Our Credo stakeholders first through pursuing the highest standards of quality, compliance, and ethics, ensuring everyday actions contribute to Our Purpose.
* We are continuing to better our understanding of clot science, through our Neuro Thromboembolic Initiative (NTI).
This is a commitment to advance the treatment of stroke through interdisciplinary collaboration and investment in clot and stroke research.
How we understand clots and their behaviour enhances our opportunity to design devices that improve patient outcomes and, overall, advance the treatment of acute ischemic stroke.
* Strong new product pipeline and the fastest growing medical device company within J&J in 2021.
* From a People perspective, we invest in our people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation.
This is empowered through our employee resource groups (ERGs) focused on further balances of gender, nationality, capability and more, including the additional attracting of qualified diverse candidates for our open roles.
Job Summary:
CERENOVUS a Johnson & Johnson company is recruiting for two Senior Research and...
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Type: Permanent Location: Galway, IE-G
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:01
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About Johnson & Johnson
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/ .
Johnson & Johnson Medical Devices is recruiting for a Senior Demand Planner to be hired in Saudi Arabia (Jeddah or Riyadh).
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.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion.
Proud to be an equal opportunity employer.
And our culture is interconnected by the shared values of Our Credo.
It's a culture that celebrates diversity and diverse perspectives.
It helps employees achieve an effective mix between work and home life and supports their efforts to have a positive impact on their communities.
Summary of the job:
A Demand planner is responsible for managing E2E SC activities for the Ethicon franchise including but not limited to
• Demand planning including key events management.
• Collaborate and align cross functional stakeholders to meet the franchise needs in short terms on order fulfillment and in long term to the growth strategy.
• Setting and improving SC metrics for KSA in line with EMEA metrics definitions.
• Bringing efficiencies in franchise SC operations.
• E2E CAPEX execution from forecasting through order fulfilment.
Directly Responsible Individual for ETHICON Business.
• S&OP process adherence in line with plan transformation requirements.
• Work with deliver team to meet the months sales value and ensure maximum fulfilment.
• E2E BU's Management - develop processes & Metrics.
• E2E CAPEX management - forecasting, order management & order execution.
• Single set of alignment between EMEA planning & multi-functional stake holders.
• KPIs:
o OTIF
o Back orders
o MAPE/BIAS
o NTS Delivery
o Inventory/ SLOB
Main Responsibilities
• Forecasting and S&OP Management:
o Maintain and understand the sales data at different aggregation levels (Brands, Sub-brands, SKUs, variants, sizes, Distribution channels, demand groups and demand locations).
o Gather information and document assumptions based on historical data, business intelligence gathered from sales, marketing, finance, retaile...
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Type: Permanent Location: Riyadh, SA-01
Salary / Rate: Not Specified
Posted: 2024-04-27 08:41:00
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Velys Clinical Specialist
The Clinical Specialist is responsible for building relationships with key accounts and provides a clinical support in Poland.
The position will develop business opportunities across the Johnson & Johnson MedTech range of products with leading clinical support and migrating Depuy Synthes new product for Account-based Business Plans.
The role is also responsible for developing long-term positive customer relationships to build customer dedication and confidence in Johnson & Johnson MedTech as a preferred supplier.
Job responsibilities
* Achieve high levels of customer happiness through customer relationships, product support and services.
* Provide a clinical support in Poland focus on Velys Robtic Assisted Solution procedure.
Include providing recommendations about new features and product improvements.
* Identify development opportunities and increase unit growth, profitability, and market share for target customers.
* Improve the efficiency and effectiveness of customer delivered health care services to patients through in-service education and training where appropriate.
* Support sales, scrub, marketing and franchise teams and other Johnson & Johnson MedTech business/functional unit members through a cooperative and constructive approach to sales meetings, internal company relationships, account development and the resolution of day-to-day business issues.
* Manage Account information through effective, timely reports and accurate customer records.
* Continuously improve product knowledge and selling related skills to provide improved service to customers which differentiate J&J MedTech from competitors.
* Work closely with marketing team in new product launch, clinical meetings & training.
* Run Training for commercial & scrub technician team.
* Reporting on cases completed
* Office/Field time 25%/75%
* Bachelor's degree (medical technology or biomedical sciences preferable)
* Min 3-5 years of experience with Medical Devices (required)
* Clinical Specialist with proven experience in Arthroplasty (strongly preferred)
* Must be able to work under pressure.
* A strong team player with excellent interpersonal, communication & presentation skills.
* Strong, proven leadership skills, driven by a passion to excel in a customer-centric and innovative organization.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2024-04-27 08:40:59
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整形外科医に対して,外科的手術に使用する生体内固定インプラント(外傷製品•人工関節製品)を取り扱い,その安全性及び有効性の啓蒙活動ならびに患者様が抱える課題へのソリューション営業を担当していただきます。
顧客のニーズに応えるべく,事業部内では専門性を保持し,外傷製品を取り扱うトラウマセールスチームと人工関節製品を取り扱うジョイントセールスチームの 2 チームでビジネスを展開しながら,ビジネス上ではシナジー効果,社内的には人材育成及びキャリアプランの可能性を最大化することに努めています。
トラウマビジネスは,四肢の外傷製品を取り扱い,歴史的にマーケットリーダーを維持し,そして今後も新製品の導入を継続的に計画しています。圧倒的な製品ポートフォリオとセールスカバレッジにより,更なるシェアアップと共に他社の追随を許さないポジションを目指しています。
ジョイントビジネスは,整形外科領域において最も大きな市場をビジネスフィールドとし,人工膝関節と人工股関節を取り扱い歴史的にトップクラスのポジションを維持しています。現在マーケットシェア No3 ですが,世界的に評価されているブランド製品を持ち,かつ投資領域であることから日本人医師のニーズに応えるべく中長期の戦略を遂行しながらシェアアップを目指しています。
両チーム共に,医師への製品プロモーション,当社製品の安全使用を目的とした手術立会い,代理店と協働した物流管理を主活動としながら患者様の QOL 向上を追及しております。[職務経験]
• 営業経験 3 年以上
[知識•技能]
•コミュニケーションスキル
•プレゼンテーションスキル
•基本的な PC スキル
[資格/免許]
•普通自動車免許
(確認項目)
•過去5年以内において,病気(病気の治療に伴う症状を含みます。)を原因として,又は原因は明らかでないが,意識を失ったことがある。
•過去5年以内において,病気を原因として,身体の全部又は一部 が,一時的に思い通りに動かせなくなったことがある。
•過去5年以内において,十分な睡眠時間を取っているにもかかわらず,日中,活動している最中に眠り込こんでしまった回数が週3回 以上となったことがある。
•過去1年以内において,次のいずれかに該当したことがある。
*飲酒を繰り返し,絶えず体にアルコールが入っている状態を3日 以上続けたことが3回以上ある。
*病気の治療のため,医師から飲酒をやめるよう助言を受けている にもかかわらず,飲酒したことが3回以上ある。
*病気を理由として,医師から,運転免許の取得又は運転を控えるよう助言を受けている。
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Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2024-04-27 08:40:57
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Field Service Engineer primary responsibility centers around technical support of Velys Digital Surgery (Orthopedics).
Serves as a liaison between commercial and support functions of the organization and holds responsibility for relevant administrative aspects of hardware field deployment.
Individual is responsible to own the customer support system in the installation, service and repair of all capital products - Velys.
Responsible for interaction with customers over the phone and in person for the handling of customer technical inquires, and complaints.
Overall responsibilities and duties:
* Perform Technical Support to internal and external customers.
* Manage account schedule and perform the installation, operation, repair and upgrades of equipment within assigned territory.
* Devises and implements preventative maintenance programs and maintains performance and service records for equipment.
* Manage region and schedule to facilitate all aspects of technical / engineering work required to support all products supported and serviced by the technical department.
* Responds to customer requests for emergency service.
Resolves cause(s), troubleshoots and takes corrective action.
* Provides guidance to customers to include Doctors, Nurses and hospital Biomedical engineers along with Field Service Specialists and/or Representatives and assists when customer happiness issues arise.
* Lead customer expectations on a regular basis before and after various interactions to ensure customer happiness.
* Completes paperwork, documentation and administrative tasks per policy and procedures.
* Handle allocated inventory and complete required audits to support thereof.
* Support installation and support of products in clinical trials, external evaluations, regulatory testing or similar.
* Responsible for ensuring personal and Company compliance with all local and Company regulations, policies, and procedures.
* Higher education degree or equivalent experience in engineering (required)
* Min 3-5 years of technical experience with Medical Devices (required)
* Readiness to be present in OR during orthopedic surgeries (required)
* Specialization in Medical Devices (strongly preferred)
* Project Management, Presentation, Good interpersonal skills
* Customer service experience, data analysis experience
* English verbal and written communication skills.
* Organization skills.
* Knowledge of Microsoft Office.
* Office/Field time 25%/75%
* Ability to travel on short notice.
* Operate company vehicle with appropriate license.
* Ability to work weekends and "off hours" as needed to support customer and business needs
* Heavy lifting of equipment and excessive standing, lifting and bending will be required.
* Respect and apply safety rules and procedures at all times
* Participate in incident investigation.
* Ability to perform...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2024-04-27 08:40:57
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Johnson & Johnson is recruiting for a Senior Manager, Mechanical Utilities, located in New Brunswick, New Jersey.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
At Engineering & Property Services (E&PS) we take care of all J&J buildings around the world providing end to end services from Real Estate, Engineering & Strategic Project Delivery to Facilities Management.
We have a profound influence on the entire J&J Enterprise, providing innovative workplaces where our employees can collaborate and grow, and delivering flexible site solutions which enable our business to best serve our important customers and patients.
This role is responsible for providing technical governance and direction as Subject Matter Expert in the field of Mechanical Building utilities for capital construction projects.
The Senior Manager, Mechanical Utilities is accountable for ownership of critical mechanical central utility Standard Design Platforms (SDP) for chiller, boiler, and air compressor plants.
A suitable candidate for this role will have knowledge and eagerness to learn, collaborate with business partners, and identify new technologies to aid in the delivery of capital projects.
This individual must have domain expertise in central plant design, energy optimization, and automation with experience in GxP environments, C&Q/validation with strong project and Construction Management skills.
Key relationships include working with E&PS stakeholders, and customers, J&J Quality, Procurement, EHS&S, Risk Management, to align on new innovations for incorporation into the Standard Design Platform (SDP) and to implement by providing technical direction to project teams and operating company standards and guidelines.
Key Responsibilities:
* Develops, shares and maintains worldwide J&J engineering standards for design, construction, operation and maintenance of Chiller, Boiler and Compressed Air Central Utility Plants.
* Serves as a focal point for industry and J&J internal engineering expertise in facility construction.
* Recommends standard solutions that increase the speed of project delivery and ultimately the delivery of J&J's final product to the patients.
* Updates and optimizes design, program, processes and/or technical platform to meet current and future needs.
* Supplies regulatory and J&J compliant solutions for manufacturing and research facilities.
* Develops innovative technology strategies in the areas of energy conservation and sustainability.
*...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-27 08:40:55
