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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
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
US121 NJ Raritan - 1000 Highway 202 S
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Description
Job Summary
* Intern operates under supervision depending on the assignment. Assists and contributes to assigned team for duration of internship.
Conducts research in assigned areas using established methodology or assists in developing methodology.
* Plans, designs and conduct experiments and analyzes and interprets the results.
Summarizes findings for presentation.
Keeps detailed records of work undertaken.
Verifies and assists in quality conduct of projects.
* Receives guidance, training, and mentoring from colleagues in planning and carrying out activities and assignments.
Duties and 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 will include some or all the following responsibilities:
* Perform basic and applied research in the area of medical device microbiology, perform experiments to answer questions pertaining to biofilm formation and control on medical devices, antimicrobial resistance, and/or bacterial virulence and human microbiome
* Collaborate with internal Ethicon or J&J associates to further Ethicon’s capabilities in understanding and producing antimicrobial and anti-infective products
* Good documentation practices, including writing test protocols, generating final reports, and documenting meeting minutes.
* Responsible for presenting business-related issues or opportunities to next management level
* Follow all Company guidelines related to Health, Safety and Environmental practices.
* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
* Perform other assigned tasks as needed.
Qualifications
* Be enrolled in an accredited college/university during the internship period
* Pursuing a Bachelor’s degree in Biology, Mic...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-06 07:15:23
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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
Job Function:
MedTech Sales
Job Sub Function:
Inside Sales -- MedTech (No Commission)
Job Category:
Professional
All Job Posting Locations:
Milwaukee, Wisconsin, United States
Job Description:
Johnson & Johnson is recruiting for Clinical Sales Specialist for located in Milwaukee, WI.
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
The overall responsibilities of the Clinical Sales Specialist position include advancing the Company’s sales of orthopedic surgical products by providing clinical and logistical expertise in hospitals and operating rooms - such as independent coverage of surgical cases, management of billing/purchase orders, logistics, and asset management.
Works under close supervision by management and in close partnership with Sales Consultants.
Key Responsibilities:
* Independently guide and assist surgeons in the operating room by providing clinical and technical support of orthopedic surgical cases.
* Advance DPS sales by serving as sole Company representative to provide direct customer support by attending surgeries and assuring that the proper equipment is available and functioning.
* Troubleshoot and apply independent judgment to respond...
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Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2025-03-06 07:15:14
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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
Job Function:
Project/Program Management Group
Job Sub Function:
Project/Program Management
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson HCS a member of the Johnson & Johnson Family of Companies, is recruiting a Transcend Global Program Director for a duration based position with an anticipated end date on or around December 2028.
This position can be located in Raritan, NJ / Tampa, FL / Zug, Switzerland
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Zug, Switzerland - Requisition Number: R-000668
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
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/.
Are you interested in joining a diverse and dynamic team that is helping improve patient care and drive innovation? Apply today!
The Transcend Global Program Director will report directly to the Senior Director, MTSC Digital Portfolio & Program Management and partner with key stakeholders including highest levels of MedTech Supply chain leadership and cross-functional partners.
The leader will advance the Transcend advance and mature the program governance and delivery execution strategy by providing insight and analysis to help senior leadership plan and prioritize throughout the lifecycle of the program from execution to hypercare.
This role will lead the overall direction, coordination, implementation, execution, control, and measurement of the Transcend program and provide guidance and direction to the Transcend regional PMO teams.
This leader will be responsible for providing quality reviews, governance, ...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-06 07:15:01
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Global Compliance Specialist
Location: Houston, Texas (Onsite, 5 days a week)
Position Summary:
The Global Compliance Specialist will report directly to the BII Director of Risk and Compliance.
This key role in the Risk Management and Compliance department focuses on ensuring compliance with regulations (both for legal and trade compliance), completing organizational filings and questionnaires, and supporting compliance research and policy writing.
The position is vital for maintaining operational efficiency while adhering to global laws and regulations.
Essential Job Functions and Responsibilities:
Global Compliance:
* Coordinate import and export activities, including audits, record-keeping, and ensuring compliance with U.S.
Customs Regulations, Export Administration Regulations, Foreign Asset Control Regulations, and Anti-boycott Regulations.
* Assign, document, and maintain Harmonized Tariff Codes (HTSUS) and Export Classification Numbers (ECCN) for all products.
* Conduct interviews and compile information for compliance with anti-corruption and other laws and regulations pertinent to the organization’s business activities.
* Develop, implement, and improve internal processes and written work instructions to maintain compliance with regulations.
* Provide training to internal users and gatekeepers on import/export requirements.
* Serve as the primary liaison with Shared Services, customs brokers, and freight forwarders for import/export documentation, licensing, and transaction screenings.
* Stay updated on regulatory changes and update internal policies as needed.
* Coordinate the valuation of imported merchandise, ensuring proper reporting of payments and customs valuation requirements.
* Work with IT to ensure system compatibility with trade compliance requirements.
Patent Administration:
* Maintain a database of patents and trademarks and their respective locations.
* Coordinate communications with intellectual property counsel and advisors.
* Log and track intellectual property registration activity as required.
Compliance Regulations & Research:
* Conduct legal and policy research, interpreting legislation and compliance standards.
* Investigate regulatory requirements, jurisdictional regulations, and government agency guidelines.
* Provide consultation on compliance matters.
* Develop and maintain a global research network.
* Prepare research findings and assist with action planning.
Compliance Policy Writing:
* Develop and draft compliance policies and procedures to support regulatory requirements.
* Assist with the distribution and implementation of compliance policies as directed by the RM&C department.
RM&C Department Support:
* Provide research or project support as assigned by the RM&C Manager.
Position Requirements:
* Highly organized, detail-oriented, and able to manage multiple competing priorities.
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-03-05 07:41:41
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Monoclonal Antibody Scientist
Join Elanco’s RBI Discovery Sciences team as a Monoclonal Antibody Scientist where you will be a key contributor to the discovery and optimization of novel biotherapeutics.
This position will be responsible for executing laboratory-based experiments to support monoclonal antibody drug discovery and engineering efforts in early research
Your Responsibilities:
* Conduct hands-on laboratory work for the discovery and engineering of monoclonal antibodies (mAbs)
* Collaborate with senior scientists and peers in a matrix environment to support the delivery of high-potential antibody therapeutics with optimized affinity and developability
* Communicate results effectively in written and oral form, including presenting findings at team meetings
* Maintain detailed electronic laboratory notebook and records of protocols, SOPs, etc.
What You Need to Succeed (minimum qualifications):
* Education: Master’s degree in Biology or related life sciences field (Biochemistry, Chemistry, Molecular Biology, Immunology) with 3-5 years of experience in the pharmaceutical and/or biotechnology industry, or Bachelor’s degree with 5-7 years of experience Strong background in molecular biology and biochemistry techniques, such as PCR, cloning, cell culture, ELISA
What will give you a competitive edge (preferred qualifications):
* Hands-on experience with display-based screening platform(s), such as phage, yeast, mammalian, or mRNA display
* Familiarity with antibody discovery workflows
* Understanding of antibody structure/function
Additional Information:
* Travel: Domestic & International Travel may be required (10%)
* Location: Global Elanco Headquarters - Greenfield, IN (New headquarters coming Q4 Indianapolis, IN)
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we a...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-05 07:33:43
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PURPOSE AND SCOPE:
Utilizing applied knowledge, the Sr.
Patient Account Representative – Collections assists the Quality Assurance department.
Ensuring services are met and established standards of quality assurance are followed.
In addition to departmental auditing, it includes performance and the development of call center staff in relation to increasing performance and departmental standards.
Principal Duties and Responsibilities:
* Understand and implement quality assurance standards
* Evaluate the adequacy of quality assurance standards
* Create sampling procedures and directions for recording and reporting quality data
* Review the implementation and efficiency of quality and inspection systems
* Document internal audits and other quality assurance activities
* Investigate patient complaints and non-adherence issues
* Collect and compile quality data
* Responsibility for tracking, researching, and responding to complaints
* Analyze data to identify areas for improvement in the quality system
* Prepare reports to communicate outcomes of quality activities
* Identify training needs and organize refresher training meetings to meet quality standards
* Evaluate audit findings
* Confirm ongoing compliance with quality and industry regulatory requirements
* Coach staff on techniques to increase performance
* Develop methods to assist staff in performance areas
* Teach/train negotiation techniques to staff
* Create various job aid training documents
* Educate staff about collection methods
* Document strategies for new approaches to handling patient calls
* Follows processes and operational policies in selecting methods and techniques for obtaining solutions
* Understands and recommends changes to policies and establishes procedures that affect immediate organization(s)
* Frequently interacts with supervisors, patients, managers, and other internal FMC employees normally involving matters between functional areas, other company divisions or departments, or customers
* Participates and presents at meetings with internal and external representatives.
Often leading a cooperative effort among members of a project team
* Interacts with internal departments and external customers, particularly in problem-resolution
* Acts as an advisor to subordinate(s) to meet schedules and/or resolve technical problems
* Assist with various projects as assigned
* Other duties as assigned
EXPERIENCE AND REQUIRED SKILLS:
* Bilingual Spanish/English required
* Must be willing to work 8 am – 5 pm CST
* Leadership experience preferred
* Quality auditing experience preferred, but not required
* Product or industry-specific experience
* Strong computer skills including Microsoft Office and databases
* Knowledge of tools, conc...
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Type: Permanent Location: Kennesaw, US-GA
Salary / Rate: Not Specified
Posted: 2025-03-05 07:32:48
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SBA Communications is a leading independent owner and operator of wireless communications infrastructure, including towers, buildings, rooftops, DAS and small cells.
We offer a competitive benefits and compensation package and are looking for team members who will thrive in our dynamic environment.
We welcome your interest in SBA.
Let us know a little about you by checking all that apply:
* You are a self-starter.
* You are resourceful and thrive in a fast-paced environment.
* You have a strong work ethic.
* You are passionate and driven to achieve results.
* You are a team player who enjoys working in a collaborative environment.
* You continuously challenge yourself to find innovative ways to improve.
You may be a perfect fit.
At SBA, we operate with the highest sense of integrity and commitment to quality.
We focus on achievement and operate with responsiveness, timeliness and accountability.
Our culture of excellence incorporates working collegially, where every team member can contribute meaningfully and make a difference.
If you are ready to make an impact, join our team!
Your Next Career Opportunity – Business Intelligence Analyst I
Review all relevant business intelligence information, including extracting data from multiple servers via SQL and Python to provide competitive landscape analysis.
What You Will Do – Primary Responsibilities
* Review the financial models for all business intelligence transactions prior to approval and closing.
* Analyze accounting documents, operational records, income, and expenses of tower site locations.
* Create financial forecasts for Senior Management to assist in better determining Organizational goals/budgets.
* Provide support with the recommendations to senior management, which may lead to a price adjustment, deal restructuring, potential termination or other actions to protect/optimize SBA assets.
* Assist in evaluating, designing, and implementing best practice business processes for the Business Intelligence department.
* Review and abstract legal documents to determine the financial impact on real estate-associated transactions and other departmental initiatives.
* Perform ongoing analysis of all site documents, operational records, income, and expenses of towers.
* Analyze present and past data, transactions, and results for the Business Intelligence Department.
* Tracking the performance, potential SBA asset risks, and financial results of the Business Intelligence Department to present to the Executive Team.
* Audit all reports ensuring documentation distributed to management is accurate.
* Initiate CRM workflows, reports, views, and processes for all groups within the BI department.
* Create workflows for CRM to automate investigations.
* Run automating data extractions using a combination of Python and SQL.
* Provide analysis of existing process/phase timelines to determine optima...
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Type: Permanent Location: Boca Raton, US-FL
Salary / Rate: Not Specified
Posted: 2025-03-05 07:29:44
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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
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
TW009 One J&J Taipei
Job Description:
Helps establish and implement programs and innovative initiatives for the organization to advance Clinical Sales - Specialty Physicians initiatives.
Contributes to projects, programs, or processes for the Clinical Sales - Specialty Physicians area.
Integrates methods based on analyses of trends and the competitive landscape to continually improve the organization's Clinical Sales - Specialty Physicians strategy.
Generates growth initiatives within the clinical sales area by reviewing consumer analytics and communicating data-driven sales and customer retention strategies.
Attends to cases in customer accounts and advises physicians on clinical attributes or techniques associated with products.
Implements growth initiatives and improves competitive positioning through innovative sales and customer retention strategies.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
This job does not require any experience.
This job is overtime eligible.
Job is eligible for sales incentive / sales commissions.
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Type: Permanent Location: Taipei City, TW-TPE
Salary / Rate: Not Specified
Posted: 2025-03-05 07:10:56
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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
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
CN002 Beijing Jianguo Road
Job Description:
Collaborates with the Medical Science Liaison team and provides expertise on scientific issues based on data-driven research.
Explores and recommends sites for clinical trials in all stages of development.
Reviews relevant medical science literature and summarizes research on new developments in products and services.
Responds to inquiries to establish and/or further the knowledge and understanding of marketed products and related topics.
Coaches more junior colleagues in techniques, processes, and responsibilities. Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-03-05 07:10:50
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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
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Statistical Programming Director to be in Titusville, NJ, Raritan, NJ or Spring House, PA, and follow a hybrid schedule of three days in the office and two days remotely per week.
The Programming Director is a highly experienced functional area leader with expert knowledge of Programming strategy concepts and processes, industry standards and complex data structures and reporting solutions. This position requires expert project and people leadership skills with the capability to effectively manage programming support across a large portfolio across one or more therapeutic areas and/or disease area strongholds, and all phases of development. This position is accountable for programming strategy and delivery of the assigned area in accordance with company and departmental processes and procedures.
In collaboration with departmental and cross-functional leadership/key stakeholders, this position also contributes to process optimization and innovation while ensuring appropriate cross-functional alignment and engagement when necessary.
As such this position is accountable to drive the overall technical capability strategy and process solutions delivering increased productivity, quality, performance and innovation within the programming functional area.
As a people and organizational leader, this position is accountable for the recruitment, performance management, talent development, and resource management within their assigned area to meet current and future business needs, contributing to the overall talent management and sourcing strategy for the department.
As a member of the Clinical & Statistical Programming (C&SP) Leadership Tea...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-05 07:10:11
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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
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson and Johnson Innovative Medicine is recruiting for a Co-Op in the Bioassay Methods Development group located in Malvern, PA.
Research & Development Co-op Overview:
At the J&J Innovative Medicine, 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.
The Co-Op, Bioassay Methods Development, will be responsible for the development of cell-based binding and immunoassays in support of potency, structure-function and residual impurity assessment. The individual will be responsible for ongoing method development, as well as the evaluation of new technologies such as multiplexing platforms and laboratory automation.
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 matched with a mentor and will focus on at least one focused project for the 6-month term.
The typical Co-op term is from May 2025 – December 2025.
Key Responsibilities:
* Work with team members to address variability in existing laboratory platform methods by integrating automation tools, specifically the ViaFlo liquid handling system and the Hamilton robot.
* Accurately recording data in a timely manner, including maintenance of detailed records in compliance with applicable GMP, safety, and environmental requirements.
The successful candidate will ensure data integrity and protocol compliance.
* Designing, troubleshooting, and executing experiments with minimal supervision. Analyzing data, interpreting results, and reporting data in laboratory ...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-05 07:10:10
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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
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Clinical Development & Research – Non-MD
Job Category:
People Leader
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
We are searching for the best talent for a Associate Director Clinical and Preclinical, located in Santa Clara, California.
#Li-Hybrid
Purpose:
You will be responsible for :
* Lead team of clinical and preclinical research professionals to develop and deliver appropriate global evidence generation strategies (preclinical studies, postmarket studies, investigator initiated, real world evidence) aligned to R&D, Regulatory, Professional Education and Commercial needs for the MONARCH Platform
* Ensure input and strong alignment from key regional MedTech leads and other strategically important countries/regions in the development of the clinical and preclinical evidence generation strategies
* Contribute and support the design of appropriate studies to meet premarket and postmarket needs
* Strengthen capability in and drive implementation of real-world evidence to deliver cost-effective evidence solutions
* Identify areas of highest impact for the MONARCH portfolio, create and implement solutions that significantly impact ROI, and communicate impact across the organization
* Develop network with key surgeons in the US and globally to assist in execution of the evidence strategy
* Lead teams to ensure appropriate interpretation and dissemination of all evidence generated, based on evidence dissemination strategy, including study reports, abstracts, manuscripts, etc.
* Support clinical and preclinical scientific discussions with regulatory agencies / notified bodies to drive support of the clinical, preclinical, and regulatory strategy, including proposed studies; review process of evidence generated for marketing authorization, line extensions, etc., including during sponsor regulatory inspections
* Provide scientific, technical, and strategic assessment and/or oversight on New Business Development opportunities, and support acquisition of innovative products/devices that will position our company for future growth and success
* Demonstrate the ability to influence, shape and lead teams
* Develop talent to provide strategic and scientific clinical and preclinical research capability, including responsibility for profess...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-05 07:09:56
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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
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Professional
All Job Posting Locations:
DE002 Robert Koch Strasse
Job Description:
Über Johnson & Johnson MedTech
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.
Erfahre mehr unter https://www.jnj.com/
Biosense Webster
Mit dem Geschäftsbereich Biosense Webster ist Johnson & Johnson führend im Bereich der kardiologischen Elektrophysiologie.
Die "Elektrophysiologie" ist ein Spezialgebiet zur Untersuchung und Behandlung von Herzrhythmusstörungen in der Kardiologie.
Die Aufgabe der Elektrophysiologie besteht darin, Herzrhythmusstörungen (insbesondere Herzrasen) bei einer Herzkatheteruntersuchung mit Hilfe von Elektrodenkathetern zu diagnostizieren und kurativ zu therapieren.
Was unser Team ausmacht
Biosense Webster ist geprägt durch einen starken Innovationscharakter sowie eine moderne und schnell, aber gesund wachsende Organisation.
Teamgeist, das richtige Mindset und eine offene Kultur machen den Erfolg und die Zufriedenheit unseres Teams aus.
Wir leben das „WIR“: wir feiern nicht nur unsere Erfolge gemeinsam, sondern es herrscht eine positive Fehlerkultur, in der bemüht sind, Herausforderungen schnell und unkompliziert, gemeinsam zu lösen.
Wir kultivieren das Lachen und haben Freude an unserer Arbeit.
Wir schätzen Charakterköpfe mit Teamgeist, die Verantwortung übernehmen, sowie innovativ und lösungsorientiert voranschreiten.
Möchtest Du auch mit Deinem Engagement mitgestalten sowie mit Leidenschaft große Ideen voranbringen? Dann werde Teil unseres Teams!
Zur Verstärkung unserer Teams in Deutschland suchen wir mehrere Associate Clinical Consultant (d/m/w) Biosense Webster im Außendienst
Region: OST
Die Position Associate Clinical Consultant (ACC) ist eine 8-monatige Einstiegsposition für P...
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Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-03-05 07:09:51
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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
Job Function:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
DE029 Aachen
Job Description:
Hauptverantwortlichkeiten:
* Konzipieren von Maßnahmen zur Optimierung von umwelt-, sicherheits- und gesundheitsrelevanten Aspekten
* Unterweisen der Belegschaft zu Themen des Umwelt-, Arbeits- und Gesundheitsschutzes
* Analysieren von Unfällen, Führen von Unfallstatistiken und Erarbeitung von Maßnahmen zur Vermeidung von Gefährdungen
* Identifizierung von Risiken und unfallauslösenden Faktoren
* Unterstützung bei der Erstellung von Gefährdungsbeurteilungen
* Durchführung von Sicherheitsbegehungen und internen Arbeitssicherheits- und Umweltaudits
* Betreuung (Erarbeitung Konzepte, Beratung, Umsetzung) und Überprüfung des Energie-, Umwelt-, Abfall- und Gefahrstoffmanagements sowie Überwachung der Einhaltung der relevanten rechtlichen Vorgaben
* Unterstützen bei der Umsetzung und Erreichung von Umweltzielen
* Betreuen und Weiterentwickeln der EHS-Programme und Prozesse
* Beratung zu und Weiterentwicklung von Betriebsanlagen, Arbeitsverfahren, Gefahrstoffen und Abfallströmen
Qualifications:
Ausbildung:
* Abgeschlossenes (Fach-)Hochschulstudium mit ingenieurswissenschaftlichem Schwerpunkt, idealerweise der Umweltingenieurwissenschaften, Sicherheitstechnik oder Vergleichbares
* Fortbildung zur Fachkraft für Arbeitssicherheit und praktische Erfahrungen im Arbeits- und Gesundheitsschutz (Anwendung von ISO 45001 ist von Vorteil)
* Qualifikation zum Umwelt-/ und Energiemanagementbeauftragten sowie zum Immissions-, Gewässerschutz und/oder Abfallbeauftragten sind von Vorteil
Erfahrung und Fertigkeiten:
* Mind.
6 Jahre Berufserfahrung in den Bereichen Arbeitssicherheit, Gesundheit und Umweltschutz, idealerweise im industriellen Umfeld
* Eigeninitiative, selbständiges Arbeiten und eine hohen Arbeitsflexibilität
* Arbeitet gerne in einem Team, gute Kommunikationseigenschaften, Spaß an der Arbeit mit Menschen
* Starke Dienstleistungsorientierung
* Lösungsorientiertes, analytisches und systematisches Arbeiten
* Sicherer Umgang mit MS Office und SAP
* Sehr gute Deutsch- und gute Englischkenntnisse
Wir bieten:
* Umfassendes Einführungsprogramm mit strukturiertem Onboarding-Plan in der gesamte...
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Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2025-03-05 07:09:51
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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
Job Function:
Pharmaceutical Sales
Job Sub Function:
Sales – Rare Diseases (Commission)
Job Category:
Professional
All Job Posting Locations:
Baton Rouge, Louisiana, United States
Job Description:
We are searching for the best talent for Rare Disease Account Manager (RAM) for Immunology Autoantibody Diseases to be in the Louisiana territory.
This position is field based.
About Immunology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Key Responsibilities:
We are seeking a highly motivated Rare Disease Account Manager to consistently achieve or exceed sales objectives within their Local Healthcare Market (LHM).
The Rare Disease Account Manager will report to a Senior District Sales Manager.
In this role, you will own the total market, developing and executing a strategy to identify patient opportunity, drive demand, and remove fulfillment barriers.
To achieve the business goals and meet customer needs, you will also ensure alignment with internal field partners, including Thought Leader Liaisons (TLLs), Area Business Specialists (ABSs), Field Reimbursement Managers (FRMs), Key Account Managers (KAMs) and Medical Science Liaisons (MSLs).
Join us in making a meaningful impact within the rare disease community!
The primary responsibilities of a RAM include the following (other duties may be assigned):
* Drive outstanding territory sales performance and product demand to ensure sales forecasts are met or exceeded within the LHM by building and sustaining strong, trusting relationships with customers and influencing key stakeholders
* Leverage company approved marketing resources to effectively demonstrate clinical value as a solution to address identified customer and patient needs.
Leverage payer acumen to educate on patient access and affordability options.
* Analyze qualitative and quantitative market data to assess business opportunities and priorit...
....Read more...
Type: Permanent Location: Baton Rouge, US-LA
Salary / Rate: Not Specified
Posted: 2025-03-05 07:09:43
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ERM is a global consulting firm, in the business of sustainability since 1971.
We partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunities for future generations.
Recognizing that environmental, health, safety, and social performance have become business-critical issues for many enterprises, ERM, as the world’s leading provider of environmental, health, and safety (EHS); risk; and environmental, social, and governance (ESG) consulting services, is helping companies deliver sustainable, safe, and compliant performance throughout all aspects of their operations.
Our Sustainable Operations team provides highly innovative services across the full breadth of EHS advisory areas such as sustainability auditing, information solutions, safety programs, compliance and management systems, training, and corporate reporting.
As part of the continued growth and innovation of our Sustainable Operations team, ERM has an opportunity for an experienced leader to join our global consulting firm as an EHS Partner and become a true owner and shareholder in a business with sustainability at its heart. We will consider strong candidates based in Houston, Texas or New Orleans, Louisiana.
The Role
As an EHS Partner, you will develop compliance, risk, assurance, and management systems for our clients in a wide range of industries.
In this role, you will partner with the world’s largest, most exciting and innovative clients to develop world-class EHS programs.
You will have access to EHS leaders at these companies that will value your expertise and ERM’s outstanding global team of experts.
You will have the opportunity to implement novel and far-reaching solutions at the nexus of compliance and sustainability.
A highly organized leader who is a strong communicator and influencer will flourish in this role.
A candidate with strong Operational Risk & EHS Management solutions experience will assume a pivotal role in shaping a growing EHS solutions practice.
In this position, you will provide intelligent and sustainable solutions that foster strategic operational processes, reduce risks, maintain compliance, increase safety, and deliver efficiencies for clients operationalizing their sustainability and ESG goals.
We seek individuals to help us drive the continued growth of ERM’s business through selling and delivering world-class services, recruiting and developing our next generation of leaders, and further advancing our reputation for EHS sustainability solutions.
Our Partnership Model Offers Unparalleled Opportunities For Leaders With Ambition, Vision And Proven Expertise
This is a Partner-level opportunity for a Principal/Director/VP-level professional looking to further their career with an equity stake in a global company that leads the field in sustainability consulting.
A career as an ERM Partn...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-03-05 07:09:05
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
As a leader within Alcoa, you can help us fulfill our purpose and realize our vision to reinvent the aluminum industry.
Be part of the team that is helping shape a better workplace with a better work-life balance and the equal opportunities that help everyone thrive.
You have the power to shape things to make them better.
About the Role:
We are searching for an Investigation & eDiscovery Specialist to join our team at Alcoa’s Corporate office in Pittsburgh, PA.
This professional will work on-site with other Cyber Defense team members to conduct digital forensic examinations, eDiscovery activities, assist with responding to incidents and cyber events, while providing support to the team.
This professional will be responsible for full ownership of the Company’s forensic examinations, eDiscovery activities, risk and incident management.
Below are additional key responsibilities:
* Lead digital forensic examinations in support of incident response investigations, as well as employment matters
* Responsible for conducting eDiscovery activities, such as data collection, data preservation, and data production
* Collaborate with internal and external counsel on legal matters and then provide guidance on technical inquiries.
This includes generating and compiling large amounts of data, preparing reports, and advising on those reports with stakeholders.
* Conduct forensic investigations or malware investigations related to cyber events and provide relevant explanation and guidance to stakeholders.
* Maintain the security tools and identify enhancement opportunities
* Oversee vendor relationships as it pertains to legal hold and forensic software
* Assist with malware analysis and event correlation using the Company’s Security Information and Event Management (SIEM) to assist in forensic analysis and cyber event response
* Stay current on emerging cyber tools, threats and detection methods
* Optimize a cyber security program that balances risk, compliance, and cost to align with the Company’s business goals and strategy by providing recommendations for improvements as the SME.
* Assist in the development of policies, procedures, and guidelines related to digital evidence handling, forensic analysis, and incident response
What you can bring to this role:
Our values – act with integrity, operate with excellence, care for people – are at the foundation of everything we do.
To be successful in this role and to play a part in our ongoing success we desire the following background:
* Bachelor’s degree in computer Forensics, Information/Cyber Security, or equivalent
* 2 years of experience with forensic or eDiscovery
* Demonstrated experience in digital forensics and/or...
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Type: Permanent Location: Pittsburgh, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-04 07:32:33
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Your Job
Are you passionate about exploring new ideas and breaking through conventional norms? At Georgia-Pacific, we share your enthusiasm for pushing boundaries and embracing creative solutions.
We constantly challenge the status quo, take calculated risks, and strive to improve the products we make.
Georgia-Pacific is seeking a Mechanical Design Engineer to support the Dixie® business with a focus on Dixie® plates, the #1 paper plate in the market.
It is a great opportunity to solve complex consumer problems by combining creative design solutions with deep understanding of materials and manufacturing principles.
The position will report to the Neenah Technical Center located in Neenah, WI with hybrid work considered.
Our Team
The Georgia-Pacific Dixie® R&D team is responsible for the technical developments that will allow the Dixie brand to maintain its position as the preferred brand of disposable plates, cups, cutlery and food packaging.
We are entrepreneurs who innovate daily and collaborate cross-functionally to design products and execute projects that create value for our consumers, customers, communities, and company.
We value lifelong learners who want to contribute and grow with us.
Our team is successful because we have self-starters who work collaboratively and leverage the diverse skills across the team to solve complicated problems, which enables everyone to maximize their contributions to business success.
What You Will Do
* Design and Experimentation: Design, experiment, and evaluate alternatives to solve complex problems and execute product roadmaps based on understanding of technical capabilities, business and market needs.
* Technology Development: Collaborate with internal and external technology partners to develop and implement new tooling design, pressed paper manufacturing, and substrate technologies into product roadmaps across lab, pilot, and commercial scales.
* Consumer Focus: Connect market and consumer needs to product performance by designing alternatives and setting technical specifications on final product design.
* Collaboration: Work with business stakeholders, innovation team, consumer research, quality, operations, and our supply partners to drive product/cost improvements by maximizing throughput, minimizing waste, and optimizing products in the portfolio.
* Risk Management: Design and execute experiments to understand and mitigate technical risk of new products by considering market feedback plus manufacturing capability.
* Product Support: Provide technical support on product claims, data substantiation, intellectual property, and overall product points of view to our business leaders, operations, manufacturing, sales, and marketing teams.
Who You Are (Basic Qualifications)
* Bachelor's degree or higher in Mechanical Engineering
* Demonstrated hands-on experience in designing, developing, and implementing tooling solutions for mechanical systems, ens...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-03-04 07:31:54
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The California Emerging Infections Program (CEIP) is a program administered by Heluna Health.
CEIP functions under a cooperative agreement with the Centers for Disease Control and Prevention (CDC), and is a collaborative effort involving the California Department of Public Health (CDPH), the University of California, Berkeley, School of Public Health, and several local health departments.
The Surveillance Officer will assist with infectious disease surveillance and related activities of the CEIP.
The applicant should possess excellent communication skills, both verbal and written.
Work will be conducted at the CEIP Oakland office.
Travel to hospitals and health departments in the San Francisco Bay Area may also be required.
Duties will include, but are not limited to, medical record data abstraction, data entry, contacting hospitals and laboratories for information regarding patients, requesting medical records, and other general organizational office work as needed.
The Surveillance Officer will also interact with local health departments regarding reportable conditions, ensuring necessary follow-up and submitting reports to the Centers for Disease Control and Prevention (CDC).
The Surveillance Officer may conduct public health interviews of case-patients (as necessary) and lead special studies under direct project coordinator supervision as assigned.
*Applicant must submit a resume and cover letter for consideration.
The salary for this role is $72,996 annually
ESSENTIAL FUNCTIONS
* Establish/maintain laboratory-based infectious disease surveillance system
* Medical record data abstraction, data entry and data edits
* Project protocol development and modification
* Assist Project Coordinator in compiling reports including feedback to participating hospitals and labs
* Attend general CEIP and core staff meetings
* Conduct follow-up with local health departments (LHD) in disease reporting and ensuring necessary follow-up for reportable conditions; assist LHD and state health dept.
in outbreak investigations
JOB QUALIFICATIONS
Education/Experience
* Master’s degree in Public Health, Epidemiology, or related field.
This may be substituted with a Bachelor’s degree in Public Health or related Science (Microbiology, Statistics, Health Science, Biology) plus 2 years of public health experience.
* Microbiology or epidemiology coursework strongly preferred.
Public Health Experience Requirement:
* Experience with infectious diseases in either academic, clinical, public health, or research setting.
* Understanding of medical terminology.
* Experience collecting data on standardized forms.
* Experience with basic data analysis (e.g., R/SAS/SPSS/STATA).
* Excellent attention to detail and organizational skills.
Candidates can demonstrate their skills in this area.
* Strong written and verbal communication skills, particularly in email communication...
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Type: Permanent Location: Oakland, US-CA
Salary / Rate: 72996
Posted: 2025-03-04 07:17:13
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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
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Professional
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
Job Description:
Johnson & Johnson is currently seeking a Clinical Sales Support to join our Johnson Med-Tech team located in Israel.
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/.
Innovation in Health & Wellness is Our Mission
"in MedTech, We Blend Heart, Science & Ingenuity, to profoundly change the trajectory of health for Humanity"
As part of the Johnson & Johnson global group, Johnson & Johnson MedTech Israel specializes in the marketing, implementing, and supporting Johnson & Johnson’s medical device solutions with a focus on surgery, orthopedics, cardiology and neurology.
Being a leader in providing access to advanced medical devices for all government-owned, public, and private healthcare providers, helping our patients live longer, healthier lives.
We at Johnson & Johnson MedTech are looking for a clinical support specialist for our Cardiovascular & Specialty solutions) department.
Key Responsibilities:
1.
Clinical Expertise:
* Provide expert clinical support during complex electrophysiology procedures, including cardiac arrhythmia diagnosis, mapping, and treatment using our advanced systems.
* Actively contribute to upgrading healthcare centers' capabilities through training and mentorship.
* Stay current with advancements in electrophysiology and related technologies to ensure exceptional support.
2.
Business Development:
* Achieve sales targets by promoting and positioning our innovative electrophysiology solutions.
* Manage a personal territory, building strategic partnerships with key hospital accounts and stakeholders.
* Develop and implement a robust business and clinical plan to achieve territory objectives.
3.
Marketing & Market Intelligence:
* Monitor and report on mark...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-03-04 07:15:55
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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
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
BE022 GENT
Job Description:
CAR-T (chimeric antigen receptor T-cell therapy) is a new way to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
The patients’ own T cells are harvested and engineered to kill the cancer cells expressing a specific antigen.
To bring this life saving therapy to the patients, Johnson & Johnson Innovative Medicine is looking for new talents to support the QA Lab organisation! So don't hesitate, the patients are waiting!
The QA Lab Associate CAR-T is responsible for providing quality oversight for the in process Lab of the CAR-T cellular therapy products in accordance with internal policies, standards, procedures, and Global cGMP’s.
Key Responsibilities:
* Provide compliance oversight for the IPL laboratories, ensuring accurate and timely review of laboratory investigations, performing analysis on quality indicating data and identifying any trends noted for QC data.
* Support drafting and approving of standard operating procedures.
* Perform spot-checks in the IPL Lab.
to ensure compliance with written regulations, policies, procedures, and global procedures.
* Ensure non-conformances are investigated thoroughly and approved in a timely manner and appropriate corrective and preventive action plans are implemented.
* Strive to reduce non-conformances in supported areas by proactively driving compliance.
* Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
* Critically support investigations and reports, interpret results, and generate technical conclusions consistent with quality risk management principles.
* Recognize patterns and trends in reported data and communicate to management.
* Provide guidance in the interpretation of quality issues and participates in the development of technical or scientific initiatives and activities.
* Routinely recognize and resolve quality issues.
Seeks management guidance on complex issues.
Develops procedures.
* Be able to interpret complex results and situations with degree of independence and articulate recommendations for solutions.
Identifies risk and develops contingency plans.
* Drive continuous improvement.
* Provide compliance oversight for Lab expansion projects i...
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Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-03-04 07:15:28
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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
Job Function:
Pharmaceutical Sales
Job Sub Function:
Sales – Rare Diseases (Commission)
Job Category:
Professional
All Job Posting Locations:
Arlington, Virginia, United States
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Rare Disease Account Manager (RAM) for Immunology Autoantibody Diseases to cover the Arlington - Washington, DC Territory.
This position is field based.
Key Responsibilities:
We are seeking a highly motivated Rare Disease Account Manager to consistently achieve or exceed sales objectives within their Local Healthcare Market (LHM).
The Rare Disease Account Manager will report to a Senior District Sales Manager.
In this role, you will own the total market, developing and executing a strategy to identify patient opportunity, drive demand, and remove fulfillment barriers.
To achieve the business goals and meet customer needs, you will also ensure alignment with internal field partners, including Thought Leader Liaisons (TLLs), Area Business Specialists (ABSs), Field Reimbursement Managers (FRMs), Key Account Managers (KAMs) and Medical Science Liaisons (MSLs).
Join us in making a meaningful impact within the rare disease community!
The primary responsibilities of a RAM include the following (other duties may be assigned):
* Drive outstanding territory sales performance and product demand to ensure sales forecasts are met or exceeded within the LHM by building and sustaining strong, trusting relationships with customers and influencing key stakeholders
* Leverage company approved marketing resources to effectively demonstrate clinical value as a solution to address identified customer and patient needs.
Leverage payer acumen to educate on patient access and affordability options.
* Analyze qualitative and quantitative market data to assess business opportunities and priorities.
* Build LHM-specific business plan and account plans to drive growth.
* Be the quarterback of the LHM team by setting the local strategy, collaborating with cross-functional LHM field partners, driving alignment, and ensuring priorities are set appropriately
* Collaborate within LHM to gain formulary status as necessary for key health systems and centers of excellence.
Influence variety of stakeholders, including C & D suite, across an account to drive adoption and pull through.
* Build and strengthen business relationships with LHM partners, such as l...
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Type: Permanent Location: Arlington, US-VA
Salary / Rate: Not Specified
Posted: 2025-03-04 07:15:22
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Sei pronto/a ad entrare a far parte di un’organizzazione in crescita, globale, specializzata nella produzione e sviluppo farmaceutico, che mette le persone al primo posto? Unisciti ad Adare! Noi lavoriamo a stretto contatto con i nostri partner nell’industria farmaceutica durante tutte le fasi di sviluppo e produzione dei farmaci destinati alla commercializzazione, con l‘intento di migliorare le vite dei/delle pazienti e dei farmaci essenziali per le persone di tutto il mondo.
Ogni ruolo all’interno di Adare ti offrirà un’esperienza unica e personalizzata nonché l’opportunità di avere un grande impatto, fondamentale per il successo della nostra azienda.
Con l’aiuto di persone come te che si dedicano alla nostra missione, Adare migliora vite migliorando la somministrazione dei farmaci!
Unisciti alla nostra missione, unisciti ad Adare!
La nostra proposta:
* Assicurazione sanitaria
* Piano pensionistico
* Benefit previsti da accordo interno
* Crescita professionale e opportunità di avanzamento all’interno dell’azienda
* Premio di partecipazione
* Programma di riconoscimento dei dipendenti.
Siamo alla ricerca di un/una Quality Control Junior Analyst (tempo determinato 6 mesi) che si unisca al nostro QC Team di Pessano con Bornago.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Quality Control Junior Analyst svolge le attività analitiche e affini all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP e dalle Procedure Operative Standard, Procedure Analitiche Standard, metodi di analisi, ed altri regolamenti interni, riportando direttamente al/alla Quality Control Laboratory Supervisor.
COMPITI E RESPONSABILITA’
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati.
* Svolge il proprio lavoro nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* Tiene in ordine ed aggiornati i propri quaderni di laboratorio e i propri documenti analitici.
* Esegue operazioni di base di laboratorio, quali: preparazione di reattivi e soluzioni, campionamenti di materie prime, prodotti semilavorati e prodotti finiti, ecc.
* Segue scrupolosamente le disposizioni impartite dai superiori.
* Esegue analisi con tecniche analitiche semplici e complesse, seguendo metodi definiti, in autonomia operativa.
* Adempie alle funzioni per la corretta gestione dei reagenti in accordo alle specifiche procedure.
* Lavora in modo efficace nel rispetto delle scadenze.
* Agisce come rappresentante dell'azienda mostrando rispetto e come ambasciatore /ambasciatrice delle convinzioni e dei comportamenti aziendali.
* Rispetta le politiche, le procedure e le normative in vigore in azienda.
* Svolge i...
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Type: Contract Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-03-04 07:15:10
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About the Role
We are seeking quality control professionals to support the site through a period of exciting growth in our wind blade manufacturing operation division. Our Quality Inspectors are responsible for performing inspections and testing in accordance with TPI and customer-specific requirements, identifying non-conforming materials, and participating in problem-solving processes to improve quality or production.
Essential Duties and Responsibilities
* Support teams on all inspections.
* Perform inspection and testing defined by TPI and customer specific requirements.
* Identify non-conforming materials or products, and draft Nonconformance Reports (NCRs).
* Provide direction, support, and training to new associates.
* Verify repairs done to the product are in conformance, with the approved methods.
* Provide a base level interpretation of engineering drawings, diagrams and confer with management or engineering staff to determine quality and reliability standards.
* Improve quality or enhance production by participating in problem solving process.
* Maintain clear and accurate inspection records (checklists, record logs, etc.).
* Use gauges like Vernier Caliper, Tape Measures, Depth Gauges etc.
* 5S measuring gauges.
* Obtains quality forms and enters data electronically.
* Reconcile final inspection documentation for release of product.
Who we're looking for
* Minimum of one (1) year quality control experience in a manufacturing environment.
* Ability to maintain safe work environment.
* Familiarity with measurement and test equipment.
* Ability to follow documented procedures and standards.
* Capability to read and interpret basic drawings and to perform basic math.
* High attention to detail.
* Excellent interpersonal and communication skills and ability to work as part of a team.
* Ability to excel in a safety-conscious, demanding and deadline driven environment.
Location
This position is on site at our wind blade manufacturing site in Newton, Iowa.
Our Mission
To deliver innovative and sustainable solutions to decarbonize and electrify the world by expanding the adoption of renewable energy.
We accomplish this by cultivating an inclusive culture that attracts, develops, excites, and retains exceptional talent.
Additional Information
TPI Composites, Inc.
offer competitive compensation and benefits, including but not limited to, health and dental insurance, 401(k) plan with company match, and paid vacation plans.
TPI Composites, Inc.
is an equal opportunity employer.
Background check and drug test required.
All your information will be kept confidential according to EEO guidelines.
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Type: Permanent Location: Newton, US-IA
Salary / Rate: Not Specified
Posted: 2025-03-04 07:13:48
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Position Overview:
TPI Composites is seeking a highly skilled and experienced Manager for our Physical Sciences Laboratory with a strong background in mechanical testing (ASTM & ISO), quality management (ISO 17025), and team leadership.
This individual will oversee a team of engineers and technicians, ensuring laboratory operations align with industry standards and best practices.
The Manager will be responsible for maintaining compliance with ISO 17025 Quality Management System, managing laboratory certifications, and driving continuous improvement initiatives.
Key Responsibilities:
* Lead and oversee a team of engineers and technicians to ensure efficient laboratory operations and high-quality testing.
* Support new location build-out and equipment relocation.
* Manage mechanical testing per recognized standards (ASTM & ISO), customer specifications, and project-based requirements.
* Review and sign off on final test reports generated in the laboratories.
* Drive continuous improvement by collaborating with lab personnel to enhance testing capabilities and streamline procedures.
* Develop and update work instructions to align with current best practices and industry standards.
* Ensure compliance with the ISO 17025 Quality Management System, maintaining audit readiness and regulatory adherence.
* Own the certification process for ISO and DNV GL lab certifications, ensuring all requirements are met and maintained.
* Assist with inventory management to ensure availability of necessary testing materials and equipment.
* Maintain a safe, clean, and organized working environment, promoting adherence to safety protocols.
Required Qualifications:
* Bachelor's degree in Materials Science, Mechanical Engineering, or a related field.
* Minimum 5-10 years related experience required (mechanical testing of composite materials or other related materials testing/characterization or analytical laboratory management).
* Working knowledge of LabView or similar graphical based control system environment for data acquisition, manipulation and analysis.
* Proven experience managing a laboratory team, including engineers and technicians.
* Extensive knowledge of mechanical testing methods per ASTM & ISO standards.
* Strong understanding of ISO 17025 Quality Management System compliance.
* Experience handling ISO and DNV GL certification processes.
* Excellent leadership, problem-solving, and organizational skills.
* Strong attention to detail with the ability to effectively manage multiple projects by prioritizing tasks, optimizing workflows, and ensuring high-quality work while consistently meeting deadlines.
Preferred Qualifications:
* M.S.
degree in Mechanical, Chemical, Material Science or Manufacturing Engineering.
Or other Advanced degree in a relevant field.
* Six Sigma or Lean Manufacturing certification.
* Experience with MS Office, incl...
....Read more...
Type: Permanent Location: Santa Teresa, US-NM
Salary / Rate: Not Specified
Posted: 2025-03-04 07:13:45
