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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:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
About Innovative Medicine
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 a Senior Process Engineer – Chromatography position in Leiden, NL!
What you will be doing: As a Sr Process Engineer, you’ll be at the heart of our operations, maintaining and improving production processes while leading supportive processes to ensure continuous improvement.
You’ll work closely with management and operations to drive decisions regarding process engineering and methods, striving to produce comprehensive processes, operational efficiencies, and alignment with production goals.
Your effective communication skills will be key as you interact with both internal and external customers.
You will be responsible for:
* You will take ownership of Operations unit objectives, including the introduction of new production processes and systems, while ensuring the smooth, validated, and compliant operation of existing chromatography-based processes.
* You’ll supervise and continuously assess process performance, ensuring it operates within regulatory limits and delivers expected output and yield.
You’ll work multi-functionally to develop improvement strategies that reduce downtime and operational losses.
* You’ll lead data collection, analysis, and reporting efforts to support continuous improvement, ensure accurate documentation, and maintain inspection readiness.
You’ll also engage in Continuous Process Verification (CPV) activities by providing insights and performing investigations.
* You’ll serve as the domain expert for chromatography operations, driving process improvements, conducting Product Impact Assessments and Change Controls, supporting audits, and leading Gemba walks to identify and implement sustainable improvements in safety, quality, and performance.
Qualifications/Requirements:
* A ...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-05-29 08:57:41
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, Dublin, Ireland, Leiden, South Holland, Netherlands, Madrid, Spain, Warsaw, Masovian, Poland
Job Description:
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):
United Kingdom - Requisition Number: R-016401
Belgium, Netherlands, Spain, Poland, Ireland - Requisition Number: R-013644
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The Clinical Project Manager is responsible for the creation and management of a subset of Studies within the Medical Affairs Deliver Unit Portfolio.
They will collect, consolidate, and report budget, timeline and FTE actuals vs.
plan and will identify potential issues for the trial through active management of the study schedule.
Major Duties & Responsibilities
* Create, manage, and maintain study schedules in PLW + For company Sponsored and Collaborative Studies; create initial study costing and support initial OOPS management up till FPI.
* Assure Clinical timelines in PLW align to mCTMS and to latest assumptions.
Ensure proper resource demand is reflected
* Develop scenarios in PLW for budget, timeline, and FTE forecasting, while generating situational operational scenarios.
* Collect, consolidate, and report financial, timeline and resource data for governance approvals and external funding partnerships. Manage scope control, FTE and OOP variances.
+ Provide necessary Portfolio Data Insights to the TA leads
* Provide necessary Portfolio Data Insights to the TA leads
* Provide support to Finance, Business Partners and Commercial Stakeholders
Additional Responsibilities may Include:
* Mentor & support onboarding of new team members, particularly those in Trial Management.
* Foster employee engagement, inclusion, and Credo Behaviors.
Principal Relationships:
Internal: Trial Delivery Leader, Trial Delivery Manager, Program Management Leaders, Clinical Trial Assistants, DAS Leaders, Trial Management Directors, representatives of Deliv...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-29 08:57:31
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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:
Business Enablement/Support
All Job Posting Locations:
Danvers, Massachusetts, United States of America
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
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
We are searching for the best talent for a Quality Review Specialist to be in Danvers, MA.
Duties and Responsibilities
* Perform reviews of Device History Records (DHR) on the production floor for compliance to procedures, including good documentation practices (GDP), documented test results within specification, and ensuring completeness of the record
* Advising personnel on good documentation practices (GDP)
* Perform review or inspection of critical manufacturing process steps to specified requirements such as in process inspections, clean room behavior and adherence to defined process parameters by performing walk-throughs of production and support areas
* Support non-conformance investigations, including cause analysis and documenting findings
* Participate in Internal and External Quality Audits and support the audit program as needed
Qualifications
* Medical device experience preferred or other highly regulated environment
* Shows ability to stay organized, pays attention to important details, and effectively handles multiple tasks and priorities.
* Ability to communicate ideas and information clearly, effectively, and frequently (oral and written)
* Quality Assurance experience & knowledge of GMP desired
* Working knowledge of SAP desired
Johnson & Johnson is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.
We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson i...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-05-29 08:57:21
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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:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Raritan, 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 a Director, Global Commercial Strategy, Precision Medicine to be base in Raritan, NJ.
Purpose:
The Director, Global Commercial Strategy, Precision Medicine will have responsibility for supporting the design & execution of J&J’s global commercial Precision Medicine (PM) strategy in close collaboration with key cross-functional stakeholders in the global and regional pharmaceutical organization.
The successful candidate should have diagnostic commercial experience and, preferably, pharma experience, be a strong leader with excellent communication and collaboration skills, possess scientific/technical aptitude and be able to translate the commercial PM strategy into execution for our therapeutic portfolio and pipeline.
Key focus will be to partner with R&D translational biomarker and diagnostic teams across therapeutic areas (TAs) on precision medicine assets in development to help ensure and accelerate their commercial success.
You will be responsible for:
Primary responsibilities for this position will include but not limited to:
* Support the design and implementation of Global Commercial PM strategy for various biomarker-driven assets in collaboration with the Global Brand Teams, Medical Affairs, Market Access, Regulatory, and Research & Development (R&D) teams across various Therapeutic Area’s (TA’s).
* Develop and implement plans for successful launch of PM programs and partnerships, ensuring seamless global access to strategic solutions that support pharmaceutical brand strategies in collaboration with internal global and regional pharmaceutical and PM partners as well as external experts and partners.
* Provide day-to-day oversight of diagnostic partnerships with testing laboratories or test manufacturers, including providing J&J input, coordinating cus...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-29 08:57:07
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Beijing, China
Job Description:
* Share the key information with all internal stakeholders in a timely manner.
Professionally interprate and analyze the impacts of new policies and regulations for product full lifecycle.
Represent JNJ to join policy-making discussion, and follow-up the development.
* Familiar with policy/ regulation developing procedure and timely involve in the development.
Timely capture the new regulation or regulation in drafting stage.
Actively contribute to the Medical Device industry associations, especially AdvaMed, Eucomed/COCIR and CAMDI, US & EU Chambers in China; and leading industry discussions on regulations & policies, closely follow-up updates from NMPA.
* Proactively work on China Medical Device regulations and policy, understanding on the relevant overseas regulations (USA, EU, Japan, and IMDRF), provide comprehensive and reasonable regulatory policy proposals, share policies and interpretation with peers and internal/external stakeholders if appropriate.
* Maintain good relationships with internal partners, including global RA, QA, R&D and Manufacture; and connect with medical device healthcare authority, such as NMPA, CMDE, etc.
and industry associations such as AdvaMed, EUCCC, etc.
Facilitate Policy workshops with NMPA and CMDE, follow up the project proposal completion, working on the process and project finalization’s evaluation.
* Lead and delivery internal policy training per needs to improve the registration process.
Participate in the review and revision of SOP and/or working guideline, to improve the process efficiency and effectiveness.
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-29 08:56:56
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of America
Job Description:
About Innovative Medicine
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
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):
* United States - Requisition Number: R-008331
* Canada - Requisition Number: R-009630
* Belgium - Requisition Number: R-009644
* United Kingdom - Requisition Number R-009647
* Switzerland - Requisition Number: R-009649
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Remote work options may be considered on a case-by-case basis and if approved by the Company.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from any location to apply.Director, Global Labeling Product Leader.
This position is a hybrid role and can be located in Raritan, NJ; Titusville, NJ; Horsham, PA.
The Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provides advice and guidance about labeling content, processes, timelines, and scie...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-29 08:56:26
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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:
Anasco, Puerto Rico, United States of America, Jacksonville, Florida, United States of America
Job Description:
Johnson & Johnson is recruiting a Manager, PMO to join its dynamic Vision Care team located in Jacksonville, FL or Anasco, PR.
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 Description:
Organizes, manages and controls projects in Surgical Vision Supply Chain; for Product Management and or Value Stream (VS) Projects.
Leads the cross-functional team and manages the development, roll-out, and implementation of all aspects of a complex supply chain program including ancillary Supply Chain initiatives (Packaging, Automation Programs)
Major Duties & Responsibilities
• Coordinates all aspects of VS project activities and is responsible for overall project success including FPOs as they relate to Operations.
• Responsible for facilitating and developing cross functional project plans, timelines, and resource requirements to ensure successful transfer and commercialization of NP and/or Execution of VS initiatives with all necessary organizations.
(Engineering, Operations, Planning, Sourcing, etc.)
• Applies highly developed management methodologies to streamline project and program management processes.
• Designs and develops industry leading quality control operating practices.
• Implements systems to monitor and track departmental goals.
• Manages projects (as assigned) from planning, execution, reporting, monitoring through stabilization and closure.
• Drives project management activities including solution design proposal, budget development, value case assessment, organization design approvals, process documentation, knowledge transfer, testing, cut-over activities, and project-related communications and pl...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2025-05-29 08:56:10
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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:
Project/Program Management Group
Job Sub Function:
R&D Project Management
Job Category:
Professional
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, 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 the role of Director, Global Functions, Data Science Digital Health. We have a strong preference for this hybrid position to be located at one of the following offices; Titusville, NJ; Raritan, NJ; New Brunswick, NJ; Spring House, PA; Horsham, PA; Cambridge, MA; or San Diego, CA.
Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
At Johnson & Johnson Innovative Medicines R&D, the Data Science & Digital Health (DSDH) function is charged with applying analytic approaches to drug discovery and development across Therapeutic Areas.
We drive and shape internal and external collaborations, working across Janssen’s Therapeutic Areas and R&D functions, including Global Development and other areas.
The Global Functions, Data Science & Digital Health (GF, DSDH) group within the R&D Data Science organization has the accountability for full scale impact across the Development pipeline via AI/ML-driven site recommendation trial design optimization, real-world evidence (RWE) generation, digital endpoints, decentralized trials, and external policy, with the key pillars being:
* Manage the development of solutions for the purpose of driving Trial Acceleration & Optimization using data science, including but not limited to:
* Enrollment modeling, feasibility analytics, country footprint expansion, advanced AI/ML modeling for predictive site recommendations
* Leverage real-world data for pat...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-29 08:55:45
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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:
R&D Product Development
Job Sub Function:
R&D Digital
Job Category:
Scientific/Technology
All Job Posting Locations:
Bangalore, Karnataka, India, Hyderabad, Andhra Pradesh, India, Mumbai, Maharashtra, India
Job Description:
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.
Within J&J Innovative Medicine, the R&D Business Technology team is the strategic information technology partner providing innovative technology solutions that enables Global Development to expertly deliver on our portfolio and helps provide transformative medicines to patients around the world while proactively improving agility, embracing innovation and creating the organization we need to deliver in the future.
The Lead Engineer will own the vision and prioritization of new technical features and improvements for our products within Clinical Data Management and Analytics to meet business needs.
This position encompasses both execution and transformation roles behind technical solutions, ensuring that the product’s architecture aligns with the technology roadmap and adheres to our engineering standards.
The role will be responsible for designing and implementing secure, scalable, and efficient cloud solutions while also overseeing operational processes to ensure efficient performance and reliability.
This role will require building strong internal and external partnerships and will collaborate daily with other team members located in US, Europe and Asia.
It uniquely combines technical and programming skills with a broad exposure to clinical data processing as well as collaboration with multiple functions in clinical development.
Key Responsibilities
Technical Leadership and Expertise:
* Define and lead all aspects of the overall engineering and technology architecture, roadmap, and technical decisions, using modern design patterns and architectural principles for the product needs in coordination with the Technical Product Manager, Product Group Lead Engineer, and Business U...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2025-05-29 08:54:45
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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 – Pulmonary Arterial Hypertension (Commission)
Job Category:
Professional
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Dayton, Ohio, United States
Job Description:
Johnson & Johnson is recruiting for Senior Territory Manager for Actelion located in Cincinnati/Dayton, OH territory including Northern KY.
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/.
Actelion is a leader in the field of pulmonary arterial hypertension (PAH).
Our portfolio of PAH treatments covers the spectrum of disease in WHO Group 1, from Functional Class (FC) II through to FC IV, with oral, inhaled and intravenous medications.
The Senior Territory Manager’s primary responsibilities include the following.
Other duties may be assigned.
* Develops new business and maintain existing business by building and sustaining strong, trusting relationships with customers and prospects
* Plans and organizes activities and resources so that sales goals are consistently met or exceeded
* Conducts speaker programs and educational symposia
* Develops business with targeted physicians including pulmonologists, rheumatologists and cardiologists
* Provides necessary information to customers including physicians, NPs, PAs, etc.
to improve their knowledge of promoted products and the uses for which they are indicated.
* Prepares and executes Business Plan for targeted customer segments
* Manages territory budget
* Works well with team members including KAM, DM, BD, MSL, SAM, TAM and PAH Pathways counselors
* Utilizes all resources to monitor and manage business frequently
REQUIRED:
* BA/BS
* Valid Driver's license in one of the 50 states
* 10 years of field sales experience in the pharmaceuticals industry including five years of specialty sales in either cardiovascular, ...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-29 08:54:36
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Principal Clinical Research Associate – Shockwave Medical (Remote) to join our team.
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.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Principal Clinical Research Associate (CRA) is responsible for the day-to-day management of a global clinical study.
The Principal CRA will be accountable for project management activities, oversight of multiple vendors and for conducting a global clinical study in compliance with applicable clinical and regulatory standards and in alignment with the business needs.
The individual is a subject matter expert in clinical research and this work is accomplished with minimal oversight, requires frequent contact with internal and external customers and is critical to the success of the business.
Essential Job Functions
* Responsible for organizing, communicating and evaluating team objectives for clinical studies.
* Participates in study design and study preparation activities, as applicable.
* Develops and revises clinical trial documentation including clinical trial protocol development, case report form (CRF) development, IRB/Ethics submissions.
* ...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-29 08:54:26
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ERM is hiring Field Biologists to conduct surveys and monitoring for special status species for large construction projects in Fresno/Tulare, California.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of a field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40+ hours/week), limited-term role with a duration of one year, and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction special status species surveys across the client’s project area.
* Work locations are often remote and require biologists to work independently.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* At least 2+ years of Biology + Other Special Status Species Experience required.
Expertise should include more than one of the following species: Fisher.
* Must have experience with delineation, installation, or maintenance of wildlife exclusion fence, environmentally sensitive areas, no work buffers, or wildlife exclusion zones.
* Familiarity with nesting bird survey protocols and/or general bird identification skills is required.
* Experience with San Joaquin Kit Fox (SJKF), California Tiger Salamander (CTS), Swainson's hawk (SWHA) a plus.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in the documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Fluency in English and Spanish is highly preferred.
Pay Transparency:
For the Field Biologist position, we anticipate the annual base pay of $74,825 – $96,901, $35.97/hr – $46.58/hr USD, limited-term, non-exempt limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant ...
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Type: Permanent Location: Carpinteria, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:55:08
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ERM is hiring Field Biologists to conduct surveys and monitoring for special status species for large construction projects in San Jacinto, California.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. The role of field biologist requires technical skills, as well as strong organizational and communication skills.
This is a full-time (40+ hours/week), limited-term role with a duration of one year, and the possibility of renewal.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction special status species surveys across the client’s project area.
* Work locations are often remote and require Biologist to work independently.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* At least 2+ years of Biology + Other Special Status Species Experience required.
Expertise should include more than one of the following species: Kangaroo Rats.
* Minimum experience requirements for these species are as follows:
+ Kangaroo Rats – Resume demonstrates ability to differentiate Kangaroo Rats from other Dipodomys species (e.g., coursework/training/experience).
* Must have experience with delineation, installation, or maintenance of wildlife exclusion fence, environmentally sensitive areas, no work buffers, or wildlife exclusion zones.
* Familiarity with nesting bird survey protocols and/or general bird identification skills is required.
* Experience with San Joaquin Kit Fox (SJKF), California Tiger Salamander (CTS), Swainson's hawk (SWHA) a plus.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in the documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Flexible availability: willingness to work weekends, holidays, and evenings as needed by the project.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Fluency in English and Spanish is highly preferred.
Pay Transparency:
For the Field Biologist position, we anticipate the annual bas...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:55:07
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ERM is hiring Environmental Inspector to oversee environmental compliance during the construction phase of a data center project in Frederick, MD.
This is a full-time (50 hours/week), limited-term role for a duration of 2 years.
RESPONSIBILITIES:
* Preparing and conducting environmental training for construction personnel.
* Conducting field inspections, monitoring and field survey work as directed.
* Interacting with and serving as a point of contact with agency officials, regulatory agency staff, landowners, contractors, clients, and other project members and conducting required agency notifications.
* Reviewing and implementing project documents and providing direction, support, and critical judgment on environmental compliance issues.
* Providing technical leadership, support, and direction to field staff. This includes participating in daily and weekly compliance and project management meetings with the Contractor, Owner, and Tennant.
* Critically assessing environmental conditions in the field to evaluate potential environmental impacts from construction.
* Evaluating potential issues and concerns ahead of construction activities.
* Overseeing the proper implementation of mitigation measures.
* Conducting environmental sampling (hydrostatic test water, soil, etc.).
* Overseeing and verifying flagging of wetland boundaries, cultural and biological resources exclusion zones, refueling zones, etc.
* Inspecting and documenting compliance with a project's environmental requirements by preparing daily written inspection reports that provide up-to-date and consistent written and photo documentation of activities observed in the field.
* Participating in various construction meetings.
* Preparing documentation to support requests for variances from environmental permits.
* Evaluating restoration activities.
* Performing additional tasks as assigned or required.
REQUIREMENTS:
* Minimum of 5 years work experience in an environmental compliance position for a company in the environmental/construction industry or as an environmental consultant.
A minimum of 8 years of experience is required for individuals without a bachelor’s degree.
* Certification as an Environmental Specialist (CES), Erosion Sediment & Stormwater Inspector (CESSWI) Certified Professional in Erosion and Sediment Control (CPESC) or similar qualification required.
Willingness to obtain any of these certifications as soon as practicable, if not already held.
* Knowledge of relevant equipment, policies, procedures, and strategies to promote effective local, state, or national security operations for the protection of people, data, property, and institutions.
* Knowledge of the practical application of engineering science and technology including applying principles, techniques, procedures, and equipment to the design and production of various goods and services including building cons...
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Type: Permanent Location: Baltimore, US-MD
Salary / Rate: Not Specified
Posted: 2025-05-28 08:54:45
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ERM is looking for a motivated, detail-oriented Managing Consultant, Hydrogeologist to join our growing team in Boston, Massachusetts.
Working under the direction of project managers and partners, the successful candidate will work on interesting site investigation and remediation projects in the northeast region and throughout the United States.
You may also have the opportunity to work on international site investigation and remediation projects. This is a great opportunity to work with ERM's technical experts to implement the latest site investigation and remediation technologies.
RESPONSIBILITIES:
* Plan and oversee field data collection, including sampling, drilling, well installation, aquifer hydraulic conductivity testing, remedial pilot tests, and remedial system operation and maintenance.
* Compile and evaluate site investigation and remedial system monitoring data.
* Synthesize site characterization and remediation information to develop and refine conceptual site models.
* Utilize conceptual site models to communicate findings, identify data gaps, and focus additional data collection efforts.
* Review investigation and remediation data developed by other consultancies and develop recommendations for additional investigation and remediation activities.
* Work closely with geographic information system experts to develop visually compelling and informative graphics.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Communicate with subcontractors, regulatory agents, tenants, and clients during field activities.
REQUIREMENTS:
* Master's degree in hydrogeology, geology, environmental engineering or related degree.
* Minimum 5 years of experience.
* Strong written/verbal communication and organization/analytical skills; experience writing detailed technical reports.
* Willingness/interest in travel for field assignments.
* Environmental field work experience and 40-hour OSHA HAZWOPER certification a plus.
* Strong commitment to safety, including following established Health and Safety protocols.
* Valid driver’s license and a good driving record.
* Ability to work independently and as part of a team.
* Detail-oriented with mechanical aptitude and hands-on trouble-shooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
For the Managing Consultant, Hydrogeologist position, we anticipate the annual base pay of $83,318 – $98,209 USD. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based...
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Type: Permanent Location: Boston, US-MA
Salary / Rate: Not Specified
Posted: 2025-05-28 08:54:43
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Chronic Care Coordinator
Location: MICHIGAN - 100% REMOTE (NOT A COMPACT STATE)
Join our mission to help transform healthcare delivery from reactive, episodic care to proactively managed patient care that prevents live-changing problems before they happen for patients with two or more chronic conditions.
We believe every patient with chronic disease deserves consistent check-ins, follow-up, and support.
The position of the Remote Chronic Care Coordinator will perform telephonic encounters with patients on behalf of our partners each month and develops detailed care plans within our care plan templates in the electronic health record.
This begins as an Independent 1099 Contractor position but offers the potential to reach full-time W2 employment (with employee benefits).
Esrun Health is seeking nurses to work part-time from their home office as independent contractors while complying with HIPAA privacy laws.
You will set your own hours and will not be held to a daily work hour schedule.
Esrun Health wants its team members to have the flexibility to balance their work-life with their home life.
Part-time team members will typically need to dedicate an average of 20-30 hours per week to care for their assigned patients.
This unique business model allows you to choose what days and what hours of the day you dedicate to care for your patients.
The Care Coordinator will be assigned a patient panel based on skill and efficiency level and is expected to carry a patient panel of a minimum of 100 patients per calendar month within the first three months of assignment.
Care Coordinators will be expected to complete encounters on 90 percent of the patients they are assigned each month unless patients are unable to participate due to current health conditions.
Compensation Structure
Esrun Health utilizes a productivity-based pay structure:
$10.00 per completed patient encounter up to 99 encounters/month.
$10.25 100-149 encounters/month
$12.00 150-199 encounters/month,
$14.00 200-249 encounters/month
$16.00 >250 encounters/month.
Payment tier increases require 3 months consistency to achieve.
There is a $1/encounter incentive compensation for bilingual nurses equal to $3/hr.
A patient encounter will take a minimum of 20 minutes (time is cumulative to include chart review time, time spent during call attempts and the non-face-to-face encounter, time for care coordination, and time spent for documentation/billing time).
Wha...
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Type: Contract Location: Lansing, US-MI
Salary / Rate: Not Specified
Posted: 2025-05-28 08:34:27
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Accounting Analyst II - RTR Operations (Korean Speaker) - (Global Business Services)
Job Description
Accounting Analyst II - RTR Operations (Korean Speaker) - (Global Business Services)
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
* Maintain assigned SAP systems by ensuring that all relevant RTR Finance master data changes for SAP security, system tables, chart of accounts, internal orders, cost centers and profit centers are appropriate, authorized and documented.
* Ensure Finance security roles are in compliance with global segregation of duties matrix.
* Provide a source of system expertise, business knowledge and problem solving capabilities to ensure sound analysis, recommendations and action programs in the maintenance and development of RTR module
* Perform period end closing for CO-PA (customer and product profitability analysis) for management reporting purposes.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business.
In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.
To succeed in this role, you will need the following qualifications:
...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-05-28 08:30:58
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At Stewart, we know that success begins with great people.
As a Stewart employee, you’ll be joining a company that was named a 2024-2025 Best Company to Work For by U.S.
News & World Report, and a 2025 Top Workplace by USA Today.
We are committed to helping you own, develop, and nurture your career.
We invest in your career journey because we understand that as you grow, so does our company.
And our priority is smart growth – by attaining the best people, investing in tools and resources that enable success, and creating a better home for all.
You will be part of an inclusive work environment that reflects the customers we serve.
You’ll be empowered to use your unique experiences, passion and skills to help our company and the communities we serve constantly evolve and improve.
Together, we can achieve our vision of becoming the premier title and real estate services company.
Stewart is a global real estate services company, providing title insurance, settlement, underwriting, and lender services through our family of companies.
To learn more about Stewart, visit stewart.com/about.
More information can be found on stewart.com.
Get title industry information and insights at stewart.com/insights.
Follow Stewart on Facebook @StewartTitleCo, on Instagram @StewartTitleCo and on LinkedIn @StewartTitle
Job Description
Job Summary
Promotes Stewart services and solutions through various outside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share.
Job Responsibilities
* Promotes Stewart services and solutions through various inside sales and marketing activities designed to ensure customer success while maximizing Stewart revenue and market share
* Typically follows existing procedures to perform routine assignments and to solve standard problems
* Analyzes basic information and standard practices to make decisions impacting work performed
* Individual contributor working with direct oversight
* Performs all other duties as assigned by management
Education
* Bachelor’s degree in relevant field preferred
Experience
* Typically requires 0-2 years of related work experience
Equal Employment Opportunity Employer
Stewart is committed to ensuring that its online application process provides an equal employment opportunity to all job seekers, including individuals with disabilities.
If you have a disability and need assistance or an accommodation in the application process, please contact us by email at careers@stewart.com.
Benefits
Stewart offers eligible employees a competitive benefits package that includes, but is not limited to a variety of health and wellness insurance options and programs, paid time off, 401(k) with company match, employee stock purchase program, and employee discounts.
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Type: Permanent Location: Bloomington, US-MN
Salary / Rate: Not Specified
Posted: 2025-05-28 08:28:41
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Title: Intelligence Analyst IV
Location: Washington D.C., Merrifield, VA
Security Clearance: Secret
Schedule: Due to the nature of law enforcement work and operation, position may require occasional support outside of core working hours, as well as intermittent weekend support, mission dependent.
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*CONTINGENT UPON AWARD
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About KACE:
When you make the decision to join KACE, you are choosing to work alongside talented professionals that have one thing in common; the passion to make a difference! KACE employees bring their diverse talents and experiences to work on critical projects that help shape the nation’s safety, security, and quality of life.
The desire to have a career that is purposeful and forward thinking is woven into every KACE employee…it’s The KACE Way.
KACE employees are; purpose driven, forward focused, open-minded, trustworthy, and invested.
The KACE Way is our commitment to our employees, to our customers, and to our communities.
Join KACE and make a difference!
Job Summary:
Serves as a technical authority in one or more intelligence disciplines.
Is responsible for planning, coordinating, and synthesizing research from other Intelligence Analysts to prepare and disseminate all-source intelligence products and responses.
Determines research methodology and work approach and revises as appropriate.
Evaluates incoming intelligence and determines pertinent data that should be directed to the attention of the Senior Intelligence Officer.
Assesses progress of research efforts and redirects efforts.
Evaluates correctness and accuracy of researched material.
Essential Functions and Responsibilities:
* Briefs intelligence assessments and positions to principals and subordinates.
* Ensure team products fulfill National-level intelligence requirements.
* Provides technical guidance to staff principals and subordinates.
* Conducts complex research and analysis of intelligence, counterintelligence, counternarcotic, organized crime operations, capabilities, and trends supporting all source intelligence and threat production.
* Leads the preparation, coordination, and implementation of intelligence production and analysis activities in support of OCDETF operations.
* Develops intelligence estimates and projections.
Presents, advocates, and defends OCDETF positions effectively within the intelligence, planning, and operational communities.
* Coordinates, develops, drafts, writes, produces, revises, and ensures completeness of intelligence plans, annexes and associated appendices that require management input.
* Formulates and prepares the intelligence plans and security portions of exercises.
* Plans and coordinates intelligence support of joint and combined exercises.
Serves as intelligence representative, liaison, site survey officer, and focal point staff officer for exercises and real-world crisis operations.
* Maintains close liaison with counterparts in other intell...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2025-05-28 08:28:01
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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:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Latina, Italy
Job Description:
About Innovative Medicine
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 MSAT Assistant Scientist to be in Borgo San Michele-Latina.
Purpose:
This position is offered on a temporary contract basis for 6 months within the Manufacturing Science and Technology Department.
The selected candidate will be an integral part of the team managing cleaning validation projects and will report directly to the MSAT Supervisor.
You will be responsible for:
* Leading cleaning validation projects at Latina, supporting New product Introduction, Life Cycle Management and Base Business
* Executing and coordinates cleaning validation exercises
* Supporting validation specialists in executing cleaning validations according to validation plan.
* Providing input to develop cleaning validation protocols, reports and other related documents.
* Coordinating activities with the manufacturing personnel, laboratories and other groups to perform cleaning validation runs and tests.
* Managing change of control of cleaning projects
* Supporting and lead investigations related to cleaning exercises.
* Managing the communication with the main supplier and stakeholder
* Supporting analysis of the new potential CIP/improvement projects for MSAT projects
* Supporting the MSAT supervisor and Manager in cleaning validation impact assessment.
Qualifications / Requirements:
* Master Degree in Engineering, Pharmacy, CTF or Chemistry
* Short experience in chemical/cosmetic/pharmaceutical industry (ideally in Oral Solid production)
* Fluent in English (B2 level and above)
* Working knowledge of SAP/ eLims/ Comet will be considered as a nice-to-have
* Ability to work in a multidepartment and dynamic environment and to deal with urgencies on the shop ...
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Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:30
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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:
Post Doc – Drug Discovery & Pre-Clinical/Clinical Development
Job Category:
Career Program
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
We are seeking a highly skilled and motivated postdoctoral scientist, with a fixed term of 2 years, o join the team of Global Safety Pharmacology located in Beerse, Belgium.
The postdoctoral scientist will focus on de-risking drug-induced peripheral neuropathies (DIPNs) to support our drug discovery and development programs.
The successful candidate will apply their expertise in neuroscience to establish translatable human in vitro models of peripheral neuropathies with robust read-outs for functional and molecular biomarkers of DIPNs and perform intricate data analyses.
Responsibilities include experiments such as 2D co-culture of hiPSC-derived sensorimotor neurons and Schwann cells, multi-electrode array recordings, and various gene and protein expression analyses.
Collaboration with cross-functional teams and a commitment to ethical research practices aligned with the 3Rs principles will be essential.
Proficiency in English and strong communication skills will facilitate effective collaboration and dissemination of findings through scientific writing and presentations.
Major Duties & Responsibilities
* Establishing in vitro platforms of drug-induced peripheral neuropathies (DIPNs) using co-culture models of hiPSC-derived peripheral neurons and human Schwann cells
* Identification, testing and validation of human-relevant biomarkers for DIPNs in the in-vitro platforms
* Define strategies whilst collaborating with cross-functional teams and establish in-vitro screening tools to assess DIPN liabilities
* Data analysis and reporting
* Development, training, conferences and writing scientific papers for publication in relevant journals
Required Knowledge, Skills, and Abilities:
* PhD in Neuroscience, Physiology, Cell Biology, or a relevant field focused on CNS and PNS safety pharmacology/toxicity
* In-depth knowledge and experience in the mechanisms of peripheral neuropathies (up to the molecular level), electrophysiology, and hiPSCs, with a proven track record
* Hands-on experience in the experimental techniques mentioned below
* hiPSC-derived sensory or motor neurons co-cultured with human Schwann cells (or other human glial cells) on microfluidic platform...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:28
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
ES024 Janssen Madrid Oficinas
Job Description:
Position Summary:
Manager Clinical Operations is accountable for the operational management and successful country execution of all phases of clinical trials within assigned therapeutic area(s) or specific role(s), including resource allocation, adherence to timelines and budget, compliance with relevant Standard Operating Procedures (SOPs), policies, Health Care Compliance (HCC) and local regulatory requirements.
The Manager Clinical Operations supports Country Head in shaping and managing local organizational structure to ensure its optimal efficiency and demonstrates effective issue management.
This individual is responsible for line management of Local Trial Managers (LTM), Site Managers (SM), Clinical Trial Assistants (CTA) and/or other GCO staff, as required.
Oversees staff performance, development, training, project assignments, workload distribution and supports issue resolution with direct reports.
Ensures alignment of local goals with organizational objectives.
Drives innovative solutions and process improvements for the assigned therapeutic area(s), country, and GCO/Global Development (GD) overall.
Principal Responsibilities:
1.
Provide line management to direct reports including setting goals and objectives, performance evaluation and talent development.
2.
Evaluate and forecast resource needs for assigned portfolio and/or other specific area of responsibility, as required and agreed with local GCO management accordingly.
3.
Responsible for deployment of the One Delivery Model through collaboration and oversight of vendors.
4.
Accountable for the acquisition of new talents and development of human resources.
5.
Guide direct reports in issue resolution and communication with involved stakeholders.
6.
Lead organizational changes and effectively communicate on priority shifts as required.
7.
Review and approve expenses in compliance with the company policies.
8.
Demonstrate leadership behaviors in alignment with J&J Leadership Imperatives.
9.
Foster an environment that encourages sharing of ideas, information and best practices (internal and external to the organization).
10.
Provide coaching and mentorship as needed, including conduct of accompanied site visits as appropriate.
11.
Define, execute or support of long ...
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Type: Permanent Location: Madrid, ES-M
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:20
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Department
In RDS R&D Reagent Research & Design - Chemistry Solutions, we set new chemical benchmarks! Based on modern synthetics and analytical methods, we design and develop a wide variety of chemical assay components for Diagnostics and Pharma.
Our task is to provide chemical solutions for diagnostic questions within the entire product portfolio.
With our expertise and broad range of methods, we also accompany the whole lifecycle of active diagnostic ingredients.
The Team
The team of nine employees with technical and scientific backgrounds works on organic chemical and biochemical syntheses, especially in the field of internal standards, metal complexes and dye chemistry.
We apply an agile and goal-oriented approach to develop high-quality tailor-made molecules for our internal and external customers, but we also don't forget to have fun at work.
What can you expect in terms of technical tasks and responsibilities?
* The focus is on research and development of reagents in the field of organic chemistry
* Performing chemical syntheses to provide complex molecular structures, particularly in metal complexes and dyes chemistry as well as their precursors, for test development and early market supply
* Production, isolation, purification, characterization, and functional evaluation of chemical or biochemical molecules
* Characterization and evaluation of synthesis products using various analytical methods (e.g., NMR, HPLC, MS) and handling complex physico-chemical equipment
* Documentation and presentation of your results
* Ensuring cross-site communication within an international project team
* Compliance with safety and environmental protection regulations as well as conducting work according to quality guidelines
* Additional responsibility for general tasks in the department, such as the maintenance and servicing of equipment
This position requires a willingness to work with hazardous substances.
Who you are
* You have completed a university degree in chemistry and additionally a PhD in the field of organic chemistry
* You are an expert in preparative organic synthesis, in particular in the synthesis of complex organic molecules and as well as in the isolation and purification methods
* You have good knowledge of dyes chemistry and their applications
* Additional experience in the field of organometallic chemistry is an advantage
* You already have experience in the design and production of ...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-05-28 08:22:08
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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!
Position Description:
At Elanco we understand the powerful role healthy animals play in making lives better.
As pets increasingly become important parts of our families, so too does the need to help them live longer, healthier, higher-quality lives.
As the global population grows, so too will the need to meet the demand for safe, affordable food for all.
Elanco has been working to empower our customers—from veterinarians to food producers to all those concerned with animal health—to address these global challenges, and advance a vision of food and companionship enriching life.
We strive to develop and deliver products safe for consumers, animals and the environment through innovation and a shared vision to enrich the life of people worldwide.
Functions, Duties, Tasks:
* Customer Value Selling – ability to execute effective sales calls through focusing on customer needs and wants to drive loyalty, value and sales
* Account Management – ability to partner with key accounts, using strong commercial acumen and customer focus, to build long-term sustainable relationships
* Data analytics – ability to derive key insights from real world data to influence and change current and future working practice of vets and farmers/ Pet owners
* Provide management/technical support – including monitoring (e.g.
diseases, management and tracking) & vet training
* Around 75% field time (with vets, customer visits and some farms), including some overnight stays
* Accountable for the attainment of sales objectives and customer value delivery through the creation, implementation and execution of strategy and tactics.
* Deliver effective working practices, relationships, record keeping and communications within Elanco
* Work closely with the Technical Consultant and wider cross-functional team and in driving solutions to customers
Minimum Qualification (education, experience and/or training, required certifications):
* Veterinary experience in the Pet health sector would be advantageous
* University Bachelor Degree...
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Type: Permanent Location: Kinsale, IE-CO
Salary / Rate: 77000
Posted: 2025-05-27 08:18:57
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Please note that this job posting is for an evergreen position and does not represent an active or current vacancy within our organization.
We continuously accept applications for this role to build a talent pool for future opportunities.
While there may not be an immediate opening, we encourage qualified candidates to submit their resumes for consideration when a suitable position becomes available.
Chronic Care Manager
Location: Remote
Join our mission to help transform healthcare delivery from reactive, episodic care to proactively managed patient care that prevents live-changing problems before they happen for patients with two or more chronic conditions.
We believe every patient with chronic disease deserves consistent check-ins, follow-up, and support.
The position of the Nurse Chronic Care Coordinator, Remote will perform telephonic encounters with patients on behalf of our partners each month and develops detailed care plans within our care plan templates in the electronic health record.
This begins as an Independent 1099 Contractor position but offers the potential to reach full-time W2 employment (with employee benefits).
Harris CCM is seeking Nurses to work part-time from their home office while complying with HIPAA privacy laws.
You will set your own hours and will not be held to a daily work hour schedule.
You will be contracted to work a minimum of 20hrs/wk.
Harris CCM wants its team members to have the flexibility to balance their work-life with their home life.
Part-time team members will typically need to dedicate an average of 20-30 hours per week to care for their assigned patients.
This unique business model allows you to choose what days and what hours of the day you dedicate to care for your patients.
The Care Coordinator will be assigned a patient panel based on skill and efficiency level and is expected to carry a patient panel of a minimum of 100 patients per calendar month.
Care Coordinators will be expected to complete encounters on 90 percent of the patients they are assigned.
Harris CCM utilizes a productivity-based pay structure and pays $10.00 per completed patient encounter up to 99 encounters/month, $10.25/encounter from 100-149 encounters/month, $12/encounter from 150-199 encounters/month, $14/encounter from 200-249 encounters/month, and $16/encounter for >250 encounters/month.
Payment tier increases require 3 months consistency to achieve.
A patient encounter will take a minimum of 20 minutes (time is cumulative).
What your impact will be:
* The role of the Care Coordinator is to abide by the plan of care and orders of the practice.
* Ability to provide prevention and intervention for multiple disease conditions through motivational coaching.
* Develops a positive interaction with patients on behalf of our practices.
* Improve revenue by creating billable CCM episodes, increasing visits for management of chronic conditions.
* Develops detailed care plans for both the doctors a...
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Type: Contract Location: Springfield, US-IL
Salary / Rate: Not Specified
Posted: 2025-05-27 08:18:41
