-
Johnson and Johnson, Inc.
is recruiting for an Associate Clinical Account Specialist (ACAS), to be located in the Memphis, TN area.
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Job Summary
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of BWI's systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding businessgoals.
The base salary for this position is $70,000.
The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus.Theannual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year.
Bonuses are awarded at the Company's discretion on an individual basis.
Thispositionis eligible fora companycarthrough the Company's FLEET program.
Employeesmay beeligible to participate inCompanyemployee benefit programssuch ashealthinsurance, savings plan,pensionplan,disability plan, vacationpay,sicktime,holidaypay,and work, personal and family time offin accordance with the terms of the applicable plans.
Additional information can be found throug...
....Read more...
Type: Permanent Location: Memphis, US-TN
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:42
-
Johnson & Johnson is currently seeking a NPI Manager to join our Lenti Viral Vector Facility located in Sassenheim .
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 Lenti Viral Vector Facility / Pollux project: Janssen Biologics B.V., part of Johnson & Johnson, is setting up a new production facility in Sassenheim.
This facility will produce lentiviral vector, which is used at the CAR-T sites for the treatment of several types of blood cancer.
The New Product Introduction team (NPI) is an essential support group in the LVV Facility.
The team has the following major roles
1.
Ensure a smooth tech transfer of new products to the shop floor.
2.
Ensures a smooth tech transfer of improvements to existing processes or develops new and improved basic processes
The NPI team is a critical team in the direct support of Operations when it comes to the introduction of new Lenti Viral Vectors.
The NPI team is key in clear translation of the developed process to a workable process and environment for the shop floor.
The NPI team always works against the high-quality standards and safety and compliance regulations that are applicable for LVV manufacturing.
The NPI team is a multifunctional team of around 10 - 15 people consisting of staff and contractor personnel.
The NPI team is one of 3 departments within the LVV facility.
The other two are: Operations Department (OPS) and CoE.
Essential Job Duties and Responsibilities
The NPI Manager provides leadership and direction for the Process leads, Manufacturing specialist resources and activities.
Partners in the LVV facility with Operations and CoE in the introduction of new products and a smooth transition from one product to the other.
Encourages and supports the identification and development of innovative solutions to problems and opportunities.
* Acts as project lead of the receiving site
* Support process fit-to-plant methodology
* Facilitates resolution of complex process- & technical problems.
* Promotes innovation initiatives for new processes, products and ideas.
* Reviews and approves technical documentation to verify compliance to technical specifications and standards.
* Communicates with internal and external departments (R&D, OPS, QA, QC, MAM, MSAT, IT) to coordinate and execute the tech transfer.
* Assigns tasks according to projected scopes including compliance and quality improvement, capacity increase, raw material qualification, and launch preparation.
* Monitors smooth ...
....Read more...
Type: Permanent Location: Sassenheim, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:41
-
Johnson & Johnson is recruiting for Sales Associate for DePuy covering Westchester County, NY (Nyack, White Plains, and Yorktown Heights).
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/ .
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Trauma: DePuy Synthes Trauma offers a comprehensive portfolio of trauma care solutions for the treatment of the most simple to the most complex trauma injuries using traditional and minimally invasive techniques.
The overall responsibilities of the Sales Associate position include providing clinical and customer support in hospitals and procedures, while ensuring customer service, sales logistics , technical expertise , and product knowledge of the highest order/level.
Sales Associates also support sales objectives , cover cases, and maintain /handle surgeon and account relationships within a geographic territory - and may offer/sell the breadth of portfolio, services, and solutions for assigned accounts.
Key Responsibilities:
* Assist DePuy Synthes sales organization in retaining and supporting further penetration with existing customers, while supporting product conversions with new customers.
Assist in the attainment of established sales goals including market share objectives in prescribed territory.
Apply knowledge of sales process, product portfolio and customer knowledge to improve sales outcomes.
* Guide and assist surgeons in the operating room through their clinical and product knowledge.
Use product knowledge to present, demonstrate , and ensure accurate utilization of DePuy Synthes products
* Support customers by attending surgeries, assuring that the proper equipment is available and performing, including ways to optimize trays; Provide Operating Room and Sterile Processing Department consultat...
....Read more...
Type: Permanent Location: White Plains, US-NY
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:40
-
Johnson & Johnson is currently seeking an EMEA Vein-to-Vein Manager to join our Advanced Therapies team located in Ghent, Belgium.
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/.
CAR-T is an advanced therapy that uses the patient's own immune system to fight the disease.
The patient's T-cells are genetically modified to eliminate cancer cells.
This groundbreaking, innovative technology offers a hopeful outlook to patients for whom other therapies have no or insufficient effect.
This role is a people leader role of Vein-to-Vein planners linked to the Ghent manufacturing facilities.
As people leader you will be responsible & accountable for the coaching and development of your team.
You will work together with the Vein-to-Vein planners to build and execute effective planning and logistics processes to ensure smooth day-to-day operations for the patient material journey.
This role requires strong partnerships skills to collaborate and align with different stakeholders (internal & external) together with a strong CAN-DO mindset to help shape the way of working of the Vein-to-Vein team and the Ghent facilities.
As an EMEA Vein to Vein manager, you will be also accountable to ensure successful launches out of Ghent - both in a clinical and commercial setting.
Key Responsibilities:
* As a people leader, you will coach and empower your team to success
* Manage resources & work allocation in the team while ensuring personal development of team members
* Build the team to prepare for future demand increases while supporting ongoing V2V operations
* Act as the point of contact towards both Clinical & Commercial partners to ensure alignment on order status, release, and shipment timing; anticipate delays and plan accordingly for the patient
* Accountable for daily alignment across all partners (operations, quality, couriers, warehouse, cryopreservation centers, etc.) to track and prioritize batch status
* Lead escalations to raise awareness, drive for progress
* Reduce cycle time of our activities
* Maintaining a strong connect with your regional counterparts to ensure we harmonize and align to the global standard
* The responsibilities of this role will continue to increase as volumes increase and our network continues to expand
Education:
* A master's degree in Engineering, Business, Supply chain or related field is required
Experience and Skills:
Required:
* 8 years of relevant industry experience (preferably in health care...
....Read more...
Type: Permanent Location: Ghent, BE-VOV
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:40
-
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.
Are you highly motivated and striving to make an impact? We invite you to learn more about our R egulatory Affairs Team at the Johnson & Johnson Family of Companies!
The Regulatory Affairs Associate Manager (MedTech) is a member of the local Regulatory Affairs department (MedTech), supporting Regulatory Affairs Lead Singapore (MedTech) for:
* Leading the team in regulatory submissions for new/existing medical devices
* Providing input to global regulatory strategies and identifying Singapore requirements for successful regulatory filings for new products/indications/changes.
This position reports to the Regulatory Affairs Lead Singapore (MedTech).
Responsibilities:
* The Regulatory Affairs Associate Manager (MedTech) will be a member of the local Regulatory Affairs department (MedTech) within the Local Operating Company (LOC), with responsibility to support Regulatory Affairs Lead Singapore (MedTech) for leading the local regulatory affairs team in regulatory submission for new/existing products including regulatory compliance for existing product licenses throughout the product lifecycle.
* Liaise and establish cooperative relationships with source company regulatory colleagues to ensure understanding of regulatory requirements in Singapore and request the documentation required for regulatory submissions.
* Leverage a solid working knowledge of the global regulatory environment, including proposed laws, regulations and guidance, to inform compliant regulatory strategies contributing to the development of business strategies.
* Engage marketing colleagues to strategize new product regulatory pathways, line extensions and changes to currently approved products and actively accelerate launch timelines.
* Manage interactions with stakeholders and distribution centres as required to ensure product supply is not disrupted.
* Build constructive relationships with the local authorities and execute regulatory strategies in compliance with relevant laws, regulations and organizational requirements necessary to obtain, and maintain legal market status.
* Monitor and evaluate the changes of local regulatory requirements and industry standards and provide regulatory intelligence to SEA and global regulatory partners.
* Participate in industry discussions for policy shaping, as required....
....Read more...
Type: Permanent Location: Singapore, SG-01
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:37
-
Johnson and Johnson is currently seeking an Associate Director, Compliance, located in Springhouse, 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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
As an Associate Director of Compliance in Bioanalytical Discovery and Development Sciences (BDDS), you will work with internal bioanalytical groups and external partners to enable high quality and compliant data with standard operation procedures and other regulatory guidelines.
This is opportunity to support all therapeutic areas within Johnson & Johnson, spanning nonclinical studies to post-market clinical development.
Key Responsibilities:
The Associate Director for Compliance in the Bioanalytical Discovery and Development Sciences (BDDS) group will have responsibility for:
* Inspection readiness and participation in Core Inspection Team in support of regulatory inspections
* Facilitate conversations for internal study and process audits which includes supporting logistics, scheduling, responses, tracking of entry of CAPAs and resolutions.
* Working with external sourcing group to ensure compliance in work being done externally.
* Ensures compliance with company standard operation procedures and other regulatory guidelines.
* Close collaboration with partnering groups such as Quality Assurance, as needed.
* Conducting effective performance management and meaningful career development conversations for employees on their team.
* May serve as delegate to the Director of Compliance for most activities, including health authority inspections.
Qualifications
Education:
* Ph.D.
degree in related fields and 5-8 years of relevant experience, or MS degree or equivalent experience with 10-15 years of relevant experience.
Ex...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:35
-
Johnson and Johnson MedTech is currently recruiting for a Manager, Embedded Software R&D.
This position will be based out of Cincinnati, OH.
(Not Remote).
At Johnson & Johnson MedTech, we are working to solve the world's most pressing healthcare challenges through innovations at the intersection of biology and technology.
We harness our deep expertise in surgery, orthopedics, vision, and interventional solutions to design healthcare solutions that are smarter, less invasive, and more personalized.
The MedTech Surgery organization was recently established to combine Ethicon's market-leading surgical portfolio with the Robotics & Digital Solutions portfolio.
The MedTech Surgical organization is comprised of: Wound Closure & Healing and Biosurgery, Endo Mechanical and Energy, OTTAVA (Surgical Robotics), MONARCH (Flexible Robotics), and MedTech Digital.
The Manager, Embedded Software R&D, will manage and lead a team of software engineers through: Detailed design, implementation, verification (unit testing, integration testing, system testing), code reviews and risk management of Class I-III medical devices, specifically electro-mechanical systems with technical leads, develop and manage the SW development process and necessary SW development tools.
The individual will set clear expectations for direct reports and establish roles and responsibilities to manage deliverables to meet business commitments.
This individual will serve as a strong technical and leadership mentor to technical staff, oversee the creation of design development plans and coach teams to execute aggressively and predictably.
This individual will hire, develop, mentor and train engineering talent and will foster the highest standards of professionalism, ethics and compliance, and actively support our compliance program-related initiatives and activities.
This individual must possess a true passion for team development, be able to develop a strong network across functions and challenge people and project teams to successfully achieve goals.
Education:
* B.S.
in Electrical Engineering, Computer Science, Systems Engineering, or equivalent; is required.
Master's Degree (business or related field) is preferred.
Required Skills and Experience:
* A minimum of 8 years of experience in embedded software development.
* A minimum of 5 years of engineering people management assigning engineers to projects tailored to their skill levels and long-term skills development.
* Strong knowledge of software engineering management within an Agile environment, both tools and process (project tracking/scheduling; document management; SW unit/verification testing; issue/bug tracking; configuration management; integration/release testing; etc.).
* Familiarity with common software development tools/platforms/languages (JIRA, GIT, QNX, Embedded Linux, Modern C , Qt).
* Experience with requirements management and application/product lifecycle management tools and infrastr...
....Read more...
Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:34
-
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/.
Johnson & Johnson Innovative Medicine is recruiting for an Active Pharmaceutical Ingredient - Proteins Co-Op located in Malvern, PA.
Research & Development Co-op Overview:
J&J R&D encompasses the development of sophisticated materials, process improvements, risk management and mechanical testing through the development process across all sectors including Pharmaceutical, Medical Device, Consumer and Corporate/Enterprise.
We offer a fast-paced cross-functional, technologically advanced, corporate environment, passionate about developing individual engineering and scientific skills.
Life as an R&D Co-op:
The R&D Co-op program provides each student with real-life hands-on experience, coaching and mentoring, networking opportunities, as well as the opportunity to meet people from various schools throughout the country.
Each Co-op will be assigned to a single function with a specific project for the 6-month term.
The typical Co-op term is from Jan 2025 - Jun 2025.
Job Description & Key Responsibilities:
We are looking for highly motivated individual with training in chemical engineering, data science, and/or process control.
The successful candidate will be part of Modeling & Simulation team within API Proteins and contribute to providing innovative technical solutions for cell culture processes.
Specifically, the candidate will use his/her scientific knowledge and problem solving ability to:
* Develop and deploy various modeling techniques (e.g., data-driven, mechanistic, and hybrid) to identify cell culture process' rate-determining components and/or parameters,
* Design orthogonal experiments and advanced process control logics,
* Execute experiments for scientific hypothesis formation and verification,
* While maintaining laboratory notebook and other technical documents according to required guidelines.
Education:
* Major in Chemical or Biochemical Engineering.
* Candidates must be actively enrolled in an accredited University for the duration of a co-op assignment pursuing a Bachelor's or equivalent experience, Master's, or PhD degree or equivalent experience.
* Minimum GPA of 2.8
Experience and Skills:
Required:
* Coursework and/or working knowledge of cell culture processes
* Hands-on experience in process modeling & simulation
* Hands-on experience in programming languages such as Python, R, or MATLAB
* Candidates must be legally authorized to work in the U....
....Read more...
Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:33
-
Overall purpose of job:
Manages submission of new product applications to the regulatory agencies.
Directs and coordinates activities concerned with the submission and approval products to government regulatory agencies.
Provides guidance to project team members regarding regulatory compliance issues.
Oversees the preparation and maintenance of regulatory submissions and files.
Ensures adherence to standard operating procedures and protocol for the rapid and timely approval of new products and regulatory support of marketed products and other products.
Interacts with regulatory agency personnel in order to expedite approval of pending application and to resolve regulatory matters.
Consults with management personal to establish strategies and prepare appropriate regulatory filings for the regulatory activities.
In general, has responsibility for projects of medium and large scope, such as accountability for regional/global/multi-functional projects.
Essential duties and responsibilities:
Functional and Technical Competencies
Leverages deep knowledge of the regulatory environment, including compliance, current and proposed laws, regulations and guidance, to develop and oversee the execution of compliant Regulatory strategies that are aligned with business objectives of the company.
Leverages a deep scientific and technical understanding of products (medical devices, biologics or pharmaceuticals).
Encourages and leads others to find ways to continuously improve, learn about new scientific, technological and Regulatory developments, develop new capabilities, and learn from past challenges and experience in order to proactively adapt to change and drive innovative thinking.
Manages projects within timeline and budget requirements by acquiring and coordinating needed resources.
Leverages in-depth knowledge of the sector, organizational vision, Regulatory Affairs function, and cross-functional business partners to make informed business decisions and create and execute business strategies.
Leverages knowledge of the healthcare environment and external marketplace.
Leadership Competencies
Guides others in defining and prioritizing key decision criteria, considering the benefits and risks of alternatives, Credo, and evaluating immediate and future implications when making business level decisions.
Quickly and effectively prioritizes critical Regulatory Affairs goals/ initiatives and manages resources in difficult, complex, or crisis situations.
Manages change by creating structure and providing clear direction when facing ambiguity and uncertainty.
Understands others' motivations, needs, and concerns even when they are difficult to discern and applies understanding to establish trust and credibility and influence others.
Creates compelling negotiating positions that build support and consensus among key stakeholders.
Challenges the positions of others to reach win-win outcomes.
Mentors others in using ve...
....Read more...
Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:32
-
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/.
Janssen Pharmaceuticals, Inc., a pharmaceutical company of Johnson & Johnson is recruiting for a Business Transformation COOP to support the Partnerships and External Supply (PES) organization.
This position is located in United States.
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.
The overall objective of this role is to provide support to PES Business Transformation Team in key operating areas including, facilitating development, growth and utilization of the PES HUB virtual office & Knowledge Center, CMO Database administration and maintenance, data automation, report generation and analytics.
The COOP will support PowerBi dashboards and develop an understanding of External Manufacturing Operations.
Key Responsibilities:
* The position is a high-volume, high accuracy role.
* Manages many internal relationships both inside and outside of the PES organization to be successful.
* Conducts data analytics and reporting in support of Business Transformation core needs.
* Creates and manages Power Automate workflows to improve efficiency by automating manual tasks or operations.
* Develops interactive Power BI dashboards to effectively visualize and consolidate complex datasets, enabling insights and data-driven decision-making.
* Collaborates with the internal team to maintain the PES tools on the Quickbase platform.
* Maintains Contract Manufacturing Organization Data Base by ensuring the database is up-to-date, and validating external manufacturing information through regular updates to the External Site Network Database.
* Ensures the PES Knowledge Center is up-to-date with new and updated materials by partnering with data owners.
* Supports the team and contributes to the overall development, implementation, and execution of PES initiatives.
* Enrolled in university for bachelor or masters program with concentration in Science, Engineering or other technical subjects preferred.
* Must be available for 40 hours a week, with working hours from 8:00 AM to 5:00 PM.
* Excellent verbal a...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:32
-
Johnson & Johnson is recruiting for Associate Clinical Consultant for Abiomed located in Utica, NY; Cooperstown, NY; Syracuse, NY; Watertown, NY; Lake George, NY; Albany, NY,
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/ .
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
In this role as an Associate Clinical Consultant, you will be responsible for demonstrating the value and impact of our Impella ® product portfolio to physicians and hospital staff.
You will advise Interventional Cardiologists and Surgeons in patient selection, partner on training, and attend implants.
As a key role on the Commercial team, you will acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all their applications.
You will provide comprehensive guidance on the appropriate use of the Impella ® devices enabling physicians and staff to deliver positive patient outcomes.
Responsibilities
* Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts
* Collect clinically relevant data, document trip results, and communicate activities with other team members and sales counterparts.
* Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all their applications.
* Attend implants and consult physicians and medical staff on appropriate use and applications .
* Collaborate with sales counterpart on awareness programs and activities in franchise.
Pay Transparency:
The anticipated base pay range for this position is $100,000 to $125,000.
The Company maintains a highly competitive sales incentive compensation program.
Under current guidelines, this position i...
....Read more...
Type: Permanent Location: Utica, US-NY
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:31
-
Provide exceptional customer service to help people live healthier lives by treating our customers/employees in a fair and ethical manner, providing a safe, clean, inclusive environment, being a responsible member of the community, providing the right products, services, and care at the right time with fair and accurate pricing.
Provide direct patient intervention by providing health and wellness services and experiences relevant to the patient as allowable by and consistent with state and federal laws.
Demonstrate the company s core values of respect, honesty, integrity, diversity, inclusion and safety.From one tiny Cincinnati grocery store more than a century ago, we've grown into what today is the nation's largest grocer with nearly 2,800 stores in 35 states operating under 28 different names.
As America's grocer, we take pride in bringing diverse teams with a passion for food and people together with one common purpose: To Feed the Human Spirit.
With a history of innovation, we work tirelessly to create amazing experiences for our customers, communities AND each other, with food at the heart of it all.
Here, people matter.
That's why we strive to provide the ingredients you need to create your own recipe for success at work and in life.
We help feed your future by providing the value and care you need to grow.
If you're caring, purpose-driven and hungry to learn, your potential is unlimited.
Whether you're seeking a part-time position or a new career path, we've got a fresh opportunity for you.
Apply today to become part of our Kroger family! Minimum
- High School Diploma or GED
- Must be 18 years old
- Meets minimum state requirements to perform the functions related to the position
- Ability to handle highly confidential information
Desired
- Any equivalent experience of a pharmacy clerk
- Any previous comparable experience
- EPRN familiarity- Support company health and wellness initiatives
- Understand and adhere to Health Insurance Portability and Accountability Act (HIPAA) regulations and the company s policies regarding the same
- Assist pharmacist in all responsibilities except those that require a pharmacist s professional judgement
- Provide a stellar customer experience while accurately and efficiently completing all steps of reception, data entry, adjudication, and product dispensing
- Understand and follow the company guidelines on the operation of the cash register and follow all cashier handling policies to prevent loss including tendering electronic fund transactions such as Credit/Debit Cards, EBT and Gift Cards, as well as cash and check transactions
- Understand and adhere to guidelines on accepting and tendering vendor coupons, limits on cash shortages and company shrink guidelines
- Answer phone and triage calls and answer inquiries as appropriate
- Complete billing procedures adequately to assure best value to the customer and the company
- Count, measure and prepare specified product using company best practices
- ...
....Read more...
Type: Permanent Location: Dayton, US-OH
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:28
-
Create an outstanding customer experience through exceptional service.
Establish and maintain a safe and clean environment that encourages our customers to return.
Assist the department manager in reaching sales and profit goals established for the department, and monitor all established quality assurance standards.
Embrace the Customer 1st strategy and encourage associates to deliver excellent customer service.
Role model and demonstrate the company's core values of respect, honesty, integrity, diversity, inclusion and safety.Based in Portland, Oregon, Fred Meyer merged with The Kroger Company in 1998.
Today, we're proudly serving Fred Meyer customers in over 120 stores throughout Oregon, Washington, Idaho and Alaska.
As part of the Kroger family of companies, we take pride in bringing diverse teams with a passion for food and people together with one common purpose: To Feed the Human Spirit.
With a history of innovation, we work tirelessly to create amazing experiences for our customers, communities AND each other, with food at the heart of it all.
Here, people matter.
That's why we strive to provide the ingredients you need to create your own recipe for success at work and in life.
We help feed your future by providing the value and care you need to grow.
If you're caring, purpose-driven and hungry to learn, your potential is unlimited.
Whether you're seeking a part-time position or a new career path, we've got a fresh opportunity for you.
Apply today to become part of our Fred Meyer family!Minimum
* Ability to handle stressful situations
* Effective communication skills
* Knowledge of basic math; counting, addition, and subtraction
Desired
* Retail experience
* Second language: speaking, reading and/or writing
* Promote trust and respect among associates
* Create an environment that enables customers to feel welcome, important and appreciated by answering questions regarding products sold within the department and throughout the store
* Gain and maintain knowledge of products sold within the department and be able to respond to questions and make suggestions about products
* Offer product samples to help customers discover new items or products they inquire about
* Inform customers of Drug GM and Home specials
* Recommend Drug GM and Home items to customers to ensure they get the products they want and need
* Review "sell by" dates and take appropriate action
* Label, stock and inventory department merchandise
* Report product ordering/shipping discrepancies to the department manager
* Display a positive attitude
* Stay current with present, future, seasonal and special ads
* Reinforce safety programs by complying with safety procedures and identify unsafe conditions and notify store management
* Practice preventive maintenance by properly inspecting equipment and notify appropriate department or store manager of any items in need of repair
...
....Read more...
Type: Permanent Location: Burlington, US-WA
Salary / Rate: 18.19
Posted: 2024-09-27 08:07:27
-
Abiomed, a member of the Johnson & Johnson Family of Companies, is currently recruiting for a Mechanical Engineer , to be located in Danvers, Ma.
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/.
I Am Abiomed | I Am Heart Recovery | Patients First!
A Mechanical Engineer II in the Post Market Engineering group plays an integral role in Abiomed's Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices.
In this position you will conduct complaint failure investigations and support CAPAs and engineering products.
This is a position designed to develop a basic and broad engineering skillset to include root cause analysis, fixture design, project management, Impella product knowledge, and cardiology clinical background.
Principle Duties and Responsibilities :
* Responsible for identifying and researching failures to improve product quality and reliability.
* Develop, record and perform various failure analysis on systems and components to identify root cause.
* Establish root cause failure analysis techniques, processes and test methods.
* Develop and manage methods for tracking process failure trends based on failure analysis results.
* Function as the lead complaint investigator.
Performing complaint investigations and working with cross functional teams as needed to determine root cause, ensuring all investigations are completed in timely manner.
* Apply statistical tools to analyze data and drive problem resolution.
* Analyze failure reports and recommend corrective action to prevent re-occurrence of problems.
* Interact with device and process development engineers to assist in corrective actions and related risk assessment.
* Identify optimum analytical approaches critical to problems.
* Drive completion of all CAPAs in a timely manner
* Assist department specific subject matter experts in root cause analysis
* Investigate complaints by reviewing clinical notes, analyzing product performance data, and by inspecting and testing returned product to determine a root cause.
* Support sustaining engineering projects by proposing drawing and specification changes, modifying engineering models and drawings, designing test fixtures, conducting testing, and analyzing data
* Lead small projects and CAPAs by developing a project plan and schedule and by adhering to design controls
* BS in Mechanical Engineering, Biomedical Engineering or dire...
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:23
-
Change lives for the better.
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/.
THE OPPORTUNITY
The AT Senior Quality Excellence Manager is reporting to Quality Excellence Director for Quality Assurance (QA) and Quality Systems (QS) for the Advanced Therapies Quality (ATQ) Platform and is responsible for driving the development and execution of End-to-End strategies that align with the overall business goals for the Advanced Therapies Quality (ATQ) Platform.
The responsibilities & impact YOU will have:
Project Management
• Develop, maintain, and execute Advanced Therapies Quality projects that forward our strategies to maximize productivity, reduce OOS, improve quality, reduce turnaround time, improve costs, and optimize QA & QC processes across the platform.
Ensure that the status of Quality projects is clearly understood by all stakeholders and that the organization is achieving its strategic goals at the optimum pace.
• Define and articulate the vision of product/digital solution to business and IT partners.
• Develop and maintain a product roadmap that outlines key features, milestones, and deliverables.
• Oversee the development and management of digital solutions for Advanced Therapies Quality (ATQ) Platform.
• Create, maintain, shape, and prioritise the product backlog, applying business expertise and understanding of business needs to ensure it is in sync with business G&O and changing priorities.
• Collaborate with key stakeholders to align digital strategies with business objectives.
• Write clear and actionable user stories with acceptance criteria and ensure that the development team understands the requirements.
• Lead cross-functional teams in the execution of Advanced Therapies Quality (ATQ) Platform digital projects, ensuring they are delivered on time, within scope, and on budget.
• Engage with Business Partners to understand and align the requirements for Advanced Therapies Quality (ATQ) Platform digital solutions as well as seize opportunities to leverage global initiatives for ATQ deployment adapted to ATQ's needs.
• Serve as the primary point of contact for digital solutions as part of the strategy within Advanced Therapies Quality (ATQ).
Performance Analysis
• Establish key performance indicators (KPIs) to measure the success of digital initiatives.
• As part of digital strategy, shape, develop and implement an effective data governance, metrics and reporting capability.
• Translate complex technical metrics ...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:21
-
About Johnson & Johnson
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/ .
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Responsible for insight mining through customer engagement to understand the unmet needs of customers and their patients so that to bring the required knowledge of innovative medicine to the healthcare professionals with the aim to bring the most advanced and best-fit treatment solution to patients.
Essential duties and responsibilities:
- Responsible to drive patient outcomes and utilization through algorithm, best practices, customer education and medical staff interaction for new and existing accounts including training needs assessment, development of suitable training plan, execution of training and any necessary follow up.
- Drive excitement, the cost-effectiveness proposition and vision of heart recovery for the patients who may benefit from Impella by working with multiple stakeholders (IC, CTS, HF, ICU) to understand and identify local dynamics and to address barriers of adoption.
- Develop meaningful relationships to keep the therapy top of mind so physicians will increase awareness of Heart Recovery Program, identify appropriate patients who may benefit and recommend the therapy.
- Responsible to support the planning and implementation of various clinical education (trainings, workshops etc) & commercial programs (tradeshows, symposiums, dinner programs etc) that align with company's mission of increasing education, awareness and adoption of hemodynamic support.
- Market products directly to hospitals by organizing structured appointments & meetings with Interventional Cardiologists, Cardiac Surgeons, Intensivists, Heart Failure Specialists, Purchasing and Administration staff.
- Identify and open new sites using st...
....Read more...
Type: Permanent Location: Mongkok, CN-91
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:20
-
Johnson & Johnson is currently seeking a Consignment Operations Analyst to join our Supply Chain team located in Bandar Sunway.
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Position Summary:
* Perform physical stock counts throughout Malaysia according to a set count schedule, as well as completing pre-count and post-count tasks.
Actively support all consignment activity including conducting stock counts, consignment reporting, monitoring consignment stock and processing consignment-related requests and documentation.
The role will have a big impact on ensuring we stay on track with compliance requirements and the overall success of our consignment program.
There will be opportunities to collaborate with cross-functional teams.
Key Responsibilities:
1.
Consignment Management
+ Perform consignment counts at customer locations throughout Malaysia, prepare pre-count documents and complete post-count duties
+ Improve inventory health at consignment location
+ Propose ideas to improve processes, reduce consignment process complexities
+ Partner with Commercial, Distributor, Supply Chain teams for process governance
+ Partner with Distributor to ensure smooth processing of stock count adjustments and troubleshoot roadblocks timely.
2.
Processes & Reporting
+ Prepare count sheet, perform stock count compilation
+ Perform other special projects and functions as assigned
+ Review and update processes and SOPs as needed
Key Business Result:
* Consignment count completed according to yearly stock count plan.
* Pre-count and post-count duties are completed to a high level of accuracy.
* Degree in Supply Chain ...
....Read more...
Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:17
-
Johnson & Johnson stellt für Shockwave mehrere Territory Manager (d/m/w) ein, die für die Regionen Bremen oder Rostock/Berlin/Neubrandenburg tätig sein werden.
Bei Johnson & Johnson glauben wir, dass Gesundheit alles ist.
Unsere Stärke im Bereich der Gesundheitsinnovation befähigt uns, eine Welt zu schaffen, in der komplexe Krankheiten verhindert, behandelt und geheilt werden und Behandlungen intelligenter, weniger invasiv und Lösungen persönlich sind.
Durch unsere Expertise in innovativer Medizin und MedTech sind wir in der einzigartigen Position, innovative Lösungen in das gesamte Spektrum der Gesundheit zu injizieren, um die Durchbrüche von morgen zu erzielen.
Wir verbinden Wissenschaft, Technologie und Entschlossenheit, um die Gesundheit der Menschheit tiefgreifend zu verbessern.
Erfahren Sie mehr unter https://www.jnj.com/
Shockwave Medical, Inc., kürzlich von Johnson & Johnson übernommen, ist ein Pionier in der Entwicklung und Vermarktung von intravaskulärer Lithotripsie (IVL), um komplexe verkalkte Herz-Kreislauf-Erkrankungen zu behandeln.
Shockwave Medical verfolgt das Ziel, einen neuen Behandlungsstandard für die medizintechnische Behandlung von atherosklerotischen Herz-Kreislauf-Erkrankungen durch die differenzierte und proprietäre lokale Abgabe von Schalldruckwellen zur Behandlung von verkalkter Plaque zu etablieren.
Um unseren Wachstumskurs weiter voranzutreiben, sind wir auf der Suche nach Talenten, die mit neuen Ideen, Elan und ihrem Einsatz mit uns den Medizinproduktemarkt gestalten möchten.
Wir suchen zum nächstmöglichen Zeitpunk t zwei
Territory Manager (d/m/w)
für den Geschäftsbereich Shockwave
Wohnort in der eines der folgenden Regionen erforderlich: Bremen oder Berlin/ Rostock/Neubrandenburg
Der Territory Manager (d/m/w) ist verantwortlich für Kaltakquise, Neukundenakquise und den Aufbau von Beziehungen, die das Umsatzwachstum der Konten und die Kundenzufriedenheit innerhalb festgelegter Produktlinien und geografischer Gebiete steigern.
Die Schwerpunkte liegen darauf, new business zu generieren und die Verkaufsziele in einem zugewiesenen Gebiet zu erreichen, während gleichzeitig außergewöhnlicher Service und Unterstützung für Ärzte geboten werden, um deren Patientenbedürfnisse zu erfüllen.
Der Territory Manager (d/m/w) ist verantwortlich für die Einzelfallbetreuung in Katheterlaboren, während er mit Ärzten und wichtigen Entscheidungsträgern zusammenarbeitet.
Aufgaben und Verantwortlichkeiten
* Neukundenakquise und neue Verkäufe durch zeitgerechte Bereitstellung und Unterstützung von Produkt- und technischen Informationen.
* Bearbeitung von Kundenaufträgen und Angeboten
* Kundenschulungen und Bereitstellung von Informationen hinsichtlich Terminologie, Funktionen und Vorteile der Produkte, um den Umsatz und die Kundenzufriedenheit zu verbessern
* Beobachten von Verkaufsentwicklungen und Produktleistungsresultaten in der Region
* Befolgung von Sicherheitsrich...
....Read more...
Type: Permanent Location: Münster, DE-NW
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:14
-
Johnson & Johnson stellt für Shockwave eine:n Therapy Development Manager (d/m/w) ein, der für die Region Berlin tätig sein wird.
Bei Johnson & Johnson glauben wir, dass Gesundheit alles ist.
Unsere Stärke im Bereich der Gesundheitsinnovation befähigt uns, eine Welt zu schaffen, in der komplexe Krankheiten verhindert, behandelt und geheilt werden und Behandlungen intelligenter, weniger invasiv und Lösungen persönlich sind.
Durch unsere Expertise in innovativer Medizin und MedTech sind wir in der einzigartigen Position, innovative Lösungen in das gesamte Spektrum der Gesundheit zu injizieren, um die Durchbrüche von morgen zu erzielen.
Wir verbinden Wissenschaft, Technologie und Entschlossenheit, um die Gesundheit der Menschheit tiefgreifend zu verbessern.
Erfahren Sie mehr unter https://www.jnj.com/
Shockwave Medical, Inc., kürzlich von Johnson & Johnson übernommen, ist ein Pionier in der Entwicklung und Vermarktung von intravaskulärer Lithotripsie (IVL), um komplexe verkalkte Herz-Kreislauf-Erkrankungen zu behandeln.
Shockwave Medical verfolgt das Ziel, einen neuen Behandlungsstandard für die medizintechnische Behandlung von atherosklerotischen Herz-Kreislauf-Erkrankungen durch die differenzierte und proprietäre lokale Abgabe von Schalldruckwellen zur Behandlung von verkalkter Plaque zu etablieren.
Um unseren Wachstumskurs weiter voranzutreiben, sind wir auf der Suche nach Talenten, die mit neuen Ideen, Elan und ihrem Einsatz mit uns den Medizinproduktemarkt gestalten möchten.
Wir suchen zum nächstmöglichen Zeitpunkt zwei
Therapy Development Manager (d/m/w)
für den Geschäftsbereich Shockwave
Wohnort in der Region Berlin erforderlich
Als Therapy Development Manager (d/m/w) sind Sie verantwortlich für die klinische Unterstützung und das Management der Coronary Sinus Reducer-Therapie, einschließlich der Akquise von Kontakten und dem Aufbau von Beziehungen, die das Umsatzwachstum der Accounts und die Kundenzufriedenheit innerhalb der Reducer-Produktlinie und Ihres zugewiesenen Gebiets steigern.
Bei Shockwave legen wir großen Wert auf klinische Exzellenz und erwarten, dass unsere Teams von allen Gesundheitsfachkräften in ihrem Gebiet als vertrauenswürdiger Partner wahrgenommen werden, der durch Schulungen und klinische Unterstützung starke Beziehungen aufbaut.
Sie sollten über Fachkenntnisse im Bereich der refraktären Angina verfügen.
In enger Zusammenarbeit mit den Fachrichtungen interventionelle Kardiologie und allgemeine Kardiologie müssen unsere Mitarbeiter flexibel sein und ihre Zeit effektiv verwalten, während sie ein exzellentes Kundenerlebnis bieten.
Aufgaben und Verantwortlichkeiten
* Entwickeln Sie Expertenwissen über den Coronary Sinus Reducer und werden Sie von den Kunden als Produktexperte anerkannt
* Zeigen Sie ein ausgezeichnetes Wissen über das breite Krankheitsfeld und übernehmen Sie die persönliche Verantwortung für die Entwicklung/Erhaltung des Produkt- und Krankheitsbereichs...
....Read more...
Type: Permanent Location: Germany, DE-HE
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:13
-
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.
Patients First | Innovation | Winning Culture | Heart Recovery
POSITION SUMMARY
The Applied Research -Critical Care team is looking for a co-op or intern to support our early-stage research and development programs.
The co-op would be responsible for developing the next-generation algorithms and supporting data analyses.
In addition, the co-op will be involved with creating and executing feasibility testing protocols.
The student will be an active voice in our weekly team meetings and provide an independent perspective as we evaluate new technologies and applications.
KEY RESPONSIBILITIES:
The student will:
• Collaborate with cross functional team members, including clinicians, data scientists in development and refinement of advanced algorithms
• Process and condition physiological signals for analysis
• Analyze retrospective pre-clinical and clinical data and generate conclusions
• Participate in team meetings and design reviews for early-stage programs REQUIREMENTS:
* Junior, Senior, or Grad student pursuing a degree in biomedical or mechanical engineering.
Electrical engineering or computer science would also be considered with relevant medical device coursework / experience.
* Knowledge of time-domain and frequency domain biomedical signal processing algorithms using MATLAB/Python or equivalent tools.
* Strong design, testing and analytical skills required (e.g.
engineering and statistical analysis)
* Demonstrated communication skills, both written and verbal
* Self-motivated and willing to learn and explore new technologies.
* Working knowledge of cardiovascular physiology is a plus
Abiomed is an Equal Opportunity Employer committed to a diverse workforce.
Abiomed will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, national origin, ancestry, age, sexual orientation, gender identity, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.
Abiomed maintains a drug-free workplace.
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:12
-
Johnson & Johnson Innovative Medicine is recruiting for a second Director, Global Strategic Marketing, Lung Cancer, located in Raritan, NJ.
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/
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
The Director, Global Strategic Marketing, Lung Cancer reports to the Sr.
Director, Global Commercial Strategy, Lung Cancer.
The Director is responsible for owning & leading the commercial strategy, launch excellence, market shaping & development, customer solutions, go-to-market model, and LCM efforts for Rybrevant and Lazcluze (amivantamab and lazertinib).
The role will contribute to optimizing the value of our global J&J Lung Cancer portfolio, by collaborating with key functions across the Global Commercial Strategy Organization (GCSO), J&J Research and Development (R&D), and J&J business regions.
Key responsibilities include, but are not limited to:
* Lead commercial strategy, launch excellence, market shaping & development, go-to-market model, and LCM efforts for Rybrevant and Lazcluze (amivantamab and lazertinib).
* Develop and deliver global marketing campaigns and associated deliverables, with cross-regional and cross-functional buy-in.
* Coordinate with business partners to ensure strategic alignment and execution.
* Establish and deliver unique solutions to elevate the customer experience.
* Partner with Regions to develop, shape and implement commercial strategies, tactics, customer solutions and messaging.
* Work closely with Medical Affairs to ensure robust publication plans and enduring/differentiating data generation and messaging.
* Collaborate with Market Access to develop value propositions that support/bolster reimbursement and approvals globally.
* Partner acros...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:07
-
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/.
JnJ Surgical Vision is focused on providing the full range of advanced optical technologies and support to help eye care professionals deliver optimal vision and lifestyle experiences to patients of all ages.
AMO Groningen BV is specialized in the development, improvement and manufacturing of state of the art surgical ophthalmic products, mainly intra-ocular lenses.
The facility consists of small and integrated Research, Development and Manufacturing teams that have strong track records.
The team is expanding and we are currently looking for a talent for the position of::
Sr.
Scientist
Tasks and responsibilities
The Optical Scientist is a key addition to IOL optics and vision science team located in The Netherlands, Europe.
He/She will be responsible for R&D activities related to the design and development of intraocular lenses and will support the development of new optical metrology for testing intraocular lenses.
Key tasks and responsibilities are:
• Participate in the development of new concepts for unique medical devices from ideation to market phase
• Support and participate in design and development of new intraocular lenses and new optical metrology for testing intraocular lenses.
• Develop test methods and validation systems to characterize new and existing intraocular lenses.
• Support requirements development, documentation of design, writing and execution of protocols and reports.
• Stay current with the status of competitive products, with cutting-edge medical device industry and with technology trends to ensure innovative product design.
Investigate and evaluate existing technologies.
• You will contribute to multi-disciplinary research teams and will be responsible for conducting independent research tasks with European research institutes.
• Work closely within a cross-functional team, with senior research staff, and also with research institutes and R&D groups in USA .
Requirements
• BS/MS/PhD in optics, physics or vision science
• Preferably 3 or more years of relevant experience
• Proficient in optical design principles, using Zemax, OSLO or other design tools to design and simulate optical systems
• Demonstrated research experience and interest in technology development
• Strong problem solving skills
• Demonstrated verbal and written communication skills
• Self-motivated, creative, flexible, positive attitude individual with the initiative and drive for timely co...
....Read more...
Type: Permanent Location: Groningen, NL-GR
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:06
-
• Provide comprehensive, approved customer training on the JJV equipment portfolio, including Refractive suite, Tear Science Catalys and Phaco equipment.
• Support commercial colleagues as requested by managers to establish application superiority of the JJV products for pre-sales clinical application customer discussions.
• Provide application optimization of individual surgeon's settings for surgery for all JJV equipment, follow up with sites to assess needs and develop solutions for the customers.
• Must interact with Sales, Marketing and Field Service teams, serving as subject matter expert regarding application and equipment issues.
• Provide 1st line application support for all equipment users in the assigned territory 24/7.
• Attend annual clinical audit sessions to stay certified as ASM
• Submit training records and clinical trip reports to Regional ASM on monthly basis
• Assist in special projects and congresses in the assigned territory and/or other markets as requested by Management
• Manage and submit expenses, product complaints and feedback, field reporting and daily activitiessee above
....Read more...
Type: Permanent Location: Taipei, TW-TPQ
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:05
-
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 Summary:
The Site Quality Lead will lead the overall management and effectiveness of the quality management system and provides overall direction to the quality function.
The Site Quality Lead will plan, execute and manage the quality management system and activities including quality engineering, quality operations and laboratories, product release, quality systems, corrective and preventive action, non-conforming system, risk management processes, document control and training systems, ensuring compliance with regulatory and company requirements.
The Site Quality Lead serves as Management Representative for the plant and European Authorized Representative (EAR) for the Mentor Legal Manufacturer located outside the EU who places a medical device on the European markets.
The Site Quality Lead has the necessary independence, authority and responsibility to maintain the plant in compliance with all applicable regulatory requirements.
He/she reviews and acts as approval authority or delegated authority, retaining responsibility for all specifications, protocols, validations, fact books, and non-conformances.
Main duties and responsibilities:
* Serves as the site Management Representative as defined in the Quality System Regulation and ISO 13485.
Performs the duties of Management Representative as defined in the appropriate Quality Manual and governing procedures.
* Serves as the Authorized Representative Person Responsible for Regulatory Compliance (AR PRRC) according to EU-MDR.
* Monitoring the quality management system as part of the Quality System Management Review and Quality Audit Program to ensure compliance all applicable regulations and standards.
* Reviewing performance of the process/system for the site at planned intervals to ensure suitability, adequacy, and effectiveness of the quality management system and to identify opportunities for improvement.
Ensuring continuous process and product improvement.
* Ensuring the promotion of awareness of regulatory requirements throughout the organization.
Communicating to the organization the importance of meeting customer, statutory, and regulatory requirements.
* Defining the purpose and objectives of the quality system in the form of the quality policy and annual quality strategic plans, which are further developed into strategic goals and objectives.
Has authority and responsibility to assure the goals supporting the objectives are attain...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:05
-
Johnson & Johnson is recruiting for a Principal Product Security Engineer to be located in Danvers, MA.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Are you passionate about security and interested in joining a community of collaborative colleagues working in a Patient First! culture? If that's you, we have an immediate opportunity for a Product Security Analyst to join the newly formed Product Security team to help ensure security is implemented by design for this top-performing medical device company.
This is an exciting opportunity to impact development initiatives that will shape future product development and industry standards.
You will own the Product Security process that includes both pre-market and post-market processes engineering teams leverage throughout the product development lifecycle.
If you are eager to leverage your security risk and compliance skills to make a difference and directly impact patient lives, this could be perfect for you.
Primary Duties and Responsibilities
* Being at the office in Danvers MA for a minimum of 3 days per week (for candidates within commutable distance to site).
* Partner with engineering teams (cloud, console, pump, etc.) to drive successful adherence to Abiomed's product security policies, processes, program objectives.
* Create, update, and improve product security processes.
* Act as a SME on cyber security matters and provide guidance to development teams.
* Advocate for proactive inclusion of cyber security input into all phases of the product life cycle, process improvements, CAPAs, strategic product road map planning.
* Deliver...
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-09-27 08:07:04
