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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:
As Farm – Senior Sales Rep, you will be part of Poultry & Swine Sales Team of Chile.
In this role you’ll be responsible for reaching sales according to each year Business Plan for the portfolio as a whole and for each one of the key brands independently, through sales in the respective B2B Poultry & Swine accounts and the respective distributors.
Your Responsibilities:
* Being capable of identifying and measure potential business opportunities of our existing portfolio and potential new registers
* Maintain a deep understanding of the products and services offered by Elanco, and the advantages and disadvantages in comparison to direct and indirect competitors.
* Develop and execute sales and add value plans for B2B accounts.
* Being able to measure and communicate productive and economic impact of the usage of the key brands of our portfolio
* Secure through follow up the Sell in & Sell Out of Distributors under your responsibility
* Develop and Follow up the execution of the MKT initiative in the accounts under your responsibility.
* Data interpretation – Use data to understand performance and spot opportunities
* Develop and Execute initiatives to promote the usage of our products through a ROI mindset for Key Brands (Surmax, Maxiban, Monteban, Hemicell, Proteck, among others)
* Maintain a continuous training mindset of new trends for the promotion of our portfolio.
* Promote and Execute usage of Elanco Key Platforms (HTSi, FSP, GVP, among others), create value and business opportunities through them
* Continuous watching of the existing stock and forecasts of the products/accounts under your responsibility to avoid stock outs, write offs, and to maintain an appropriate safety stock.
* Being able to pull sales through the business ASK.
* Approach to customers with a long term approach and mindset
* Connect with internal Elanco resources, international peers, international consultants and others to creatively expand network inside customers and accounts under your r...
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Type: Permanent Location: Santiago, CL-RM
Salary / Rate: 33187000
Posted: 2025-06-04 08:50:35
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Senior Software Developer
Harris Local Government - Remote
Job Duties and Responsibilities
Analyze business requirements; identify product impact and possible implementation options and recommend the solution that best suits the needs of the customers and HLG.
* Create and maintain application code that meets design specifications, follows HLG standards, and is easy to maintain.
* Perform code review for technical accuracy, standards, and functional compliance to the requirements.
* Provide Level 2 support of our applications.
* Ability to estimate work as requested.
* Work within deadlines in relation to product release timelines, and consistently complete assigned development tasks in required timeframes.
* Fulfill administrative reporting requirements.
* Other duties as assigned by management.
* Minimal travel required.
EXPERIENCE / SKILLS
Required:
* Bachelor's Degree or equivalent work experience in Computer Science or related discipline.
* 5+ years of IBM AS/400 (PowerSystems) RPG-ILE programming experience.
* Experience with IBM AS/400 (Power Systems) hardware/software migrations.
* Experience with troubleshooting hardware issues with IBM AS/400 (Power Systems) and peripherals attached to them.
* Experience with software requirements specifications, and strong interpretative skills to understand design requirements.
* Experience developing software in a team environment.
* Great communication skills, both verbal and written, that includes ability to communicate with internal and external people as changes occur in tasks assigned.
* Customer-service orientation
* Able to work independently as well as part of a team.
* IBM DB2 experience
Preferred, but not required
* Experience with unit/integration/automation testing.
* Knowledge of county government software operations, billing or financial systems.
* Knowledge of VTL and RDX drives and Evault cloud backup.
* Basic knowledge of IBM Web Instances and PHP helpful.
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About Harris:
Harris is a leading provider of mission critical software to the public sector in North America.
As a wholly owned subsidiary of Constellation Software Inc.
(“CSI”, symbol CSU on the TSX), Harris has become the cornerstone for CSI’s investment in utility, local government, school districts, public safety, and healthcare software verticals.
Our success has been realized through investments in our proprietary software and market expertise.
This focus, combined with acquiring businesses that build upon or complement our offerings, has helped drive our success.
Harris will continue to growth through reinvestment – bot...
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Type: Permanent Location: Harrisburg, US-PA
Salary / Rate: 95000
Posted: 2025-06-04 08:46:42
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INVISTA is seeking a highly organized and detail-oriented Document Controller who will transition into the role of EDMS (Electronic Document Management System) Expert.
This role is pivotal in ensuring the integrity, accessibility, and compliance of engineering and project documentation while leading continuous improvement of our EDMS platform.
Our Location
This role is based on the north side of Houston, in the Greenspoint area.
This position offers a flexible hybrid schedule, allowing for a blend of remote and on-site work to support work-life balance and productivity.
This person should be prepared to work on-site as needed to collaborate effectively with team members and engage with projects that require in-person attention.
What You Will Do
Document Control Operations
* Proactively manage the lifecycle of engineering and project documentation, including version control, metadata tagging, and secure storage.
* Coordinate document reviews, approvals, and transmittals using automated workflows.
* Maintain compliance with internal standards and regulatory requirements.
EDMS Implementation & Ownership
* Become a Subject Matter Expert (SME) for the EDMS platform (e.g., Meridian).
* Develop a deep understanding of the business and end-user requirements.
Stay updated with the latest advancements in the tool sets.
* Collaborate with business stakeholders to continuously improve document control workflows.
* Understand the needs of the organization analyze issues with the system, identify patterns, and propose effective solutions.
Training & Change Management
* Develop and deliver training programs for EDMS users and document controllers.
* Provide ongoing support and troubleshooting for EDMS-related issues.
* Enhance best practices and advocate digital document management processes and procedures across the organization.
Who You Are (Basic Qualifications)
* 5+ years of experience in document control within engineering, construction, or industrial project environments.
* Proven experience administering or supporting an EDMS platform.
* Strong understanding of document lifecycle management, metadata structures, and workflow automation.
* Proficiency in Microsoft 365 (SharePoint, Excel, Word, PowerPoint).
* Excellent organizational and communication skills.
* This role is not eligible for sponsorship.
What Will Put You Ahead
* Experience with system configuration, user role management, and permission structures.
* Familiarity with ISO 9001, ISO 14224, or other document control standards.
* Ability to interpret and apply document control procedures in an IP environment.
* Experience supporting audits and compliance reviews through EDMS reporting and traceability.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compens...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-06-04 08:45:03
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Azubi Papiertechnologe/-in (m/w/d)
Job Description
Für den Ausbildungsstart 2025 suchen wir Auszubildende für den Beruf des/der Papiertechnologen/-in (m/w/d)
Beginn: 01.08.2025
Dauer: 3 Jahre
Ausbildungsorte: Kimberly-Clark Werk Koblenz, Industrie-Lehrwerkstatt (ILW) Koblenz, Papierzentrum Gernsbach (Schwarzwald)
Du lernst gerne, bist eine geborene Führungspersönlichkeit und ergreifst stets die Initiative, um Dinge zu verbessern und andere mitzureißen.
Du lebst dein Leben im Einklang mit den höchsten Werten von Integrität und Qualität und sorgst dafür, dass deine Aufgaben zu einer langfristigen Erfolgsgeschichte beitragen.
In dieser Position hilfst du uns dabei, eine bessere Pflege für Milliarden von Menschen auf der ganzen Welt zu gewährleisten.
Es beginnt mit DIR.
Ob Praktikum oder Ausbildung: Zur Gestaltung der Welt von morgen gehört für uns auch die Ausbildung junger Menschen und die Förderung von Nachwuchstalenten.
Wir möchten dir helfen, deine Ziele zu erreichen.
Deine Aufgaben:
* Überwachung und Steuerung der Arbeitsprozesse in der Papier- und Zellstoffherstellung
* Aufbereitung von Altpapier und Abwasser
* Herstellung von Hygiene-Papier als Rohstoff zur Weiterverarbeitung
* Erlernen der Grundkenntnisse in der Mechanik sowie Regel- und Messtechnik
Über uns
Kleenex®.
Huggies®.
Camelia®.
Cottonelle®.
Little Swimmers®.
Kimberly-Clark Professional®.
Du kennst unsere legendären Marken bereits - und der Rest der Welt auch.
Millionen von Menschen verwenden täglich Produkte von Kimberly-Clark.
Wir wissen, dass es diese fantastischen Produkte von Kimberly-Clark ohne talentierte Fachleute wie dich nicht gäbe.
Bei Kimberly-Clark bist Du Teil des besten Teams, das sich für Innovation, Wachstum und Wirkung einsetzt.
Wir können auf über 150 Jahre Marktführerschaft zurückblicken und sind immer auf der Suche nach neuen und besseren Wegen, um unsere Leistung zu verbessern - die Tür steht Dir also offen.
Bei Kimberly-Clark ist alles für Dich da.
Geleitet vom Ziel.
Angetrieben von Dir.
Über Dich
Du erbringst Höchstleistungen und schätzt eine Leistungskultur, die von echter Fürsorge getragen wird.
Du möchtest zu einem Unternehmen gehören, das sich aktiv für Nachhaltigkeit, Inklusion, Wohlbefinden und berufliche Entwicklung einsetzt.
Du liebst, was du tust, vor allem dann, wenn deine Arbeit einen Unterschied macht.
Bei Kimberly-Clark sind wir ständig auf der Suche nach neuen Ideen, wie, wann und wo wir die besten Ergebnisse erzielen können.
In einer unserer Positionen in der Produktion konzentrierst du dich darauf, Kunden zu gewinnen, wobei Sicherheit, gegenseitiger Respekt und Menschenwürde im Mittelpunkt stehen.
Um in dieser Position erfolgreich zu sein, benötigst du folgende Qualifikationen:
* einen guten mittleren Bildungsabschluss (Lebenslauf und Zeugnisse bitte anhängen)
* logisches Denk- und Auffassungsvermögen
* gute Mathe-, Physik- und Chemiekenntn...
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Type: Permanent Location: Koblenz, DE-RP
Salary / Rate: Not Specified
Posted: 2025-06-04 08:44:29
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Thank you for your interest in a career at NeighborHealth, formerly East Boston Neighborhood Health Center!
As one of the largest community health centers in the country, NeighborHealth is proud to serve the greater Boston area with a strong commitment to the health and well-being of our patients and communities.
Whether you're a nurse or physician providing direct care, a manager leading dedicated teams, or part of the essential support staff who keep our operations running smoothly — every role at NeighborHealth is vital.
Together, we’re advancing medicine and delivering the best care experience for our patients and community!
Interested in this position? Apply online and create a personal candidate account!
Current Employees of NeighborHealth- Please use our internal careers portal to apply for positions.
To learn more about working at NeighborHealth and our benefits, please visit out our Careers Page.
Time Type:
Full time
Department:
Quality
All Locations:
10 Gove Street – Taylor Building, 79 Paris Street
Position Summary:
NeighborHealth is seeking a Population Health Coordinator to join our team of nurses, social workers, community health workers, providers, and pharmacists, where you will have the opportunity to make a profound impact on the lives of underserved individuals and families. You will provide a critical role by successfully supporting the quality improvement, outreach, clinical operations, and population health efforts of key strategic initiatives within our department and across the health center.
* Leads or supports clinical operations workflow development and iterative improvement as assigned
* Ability, willingness, and motivation to learn and apply population health and quality improvement principles
* Develops relationships with key stakeholders across the enterprise as needed/directed.
* Assist with implementing and monitoring workflow and/or screening fidelity as directed
* Oversees volunteers for outreach as needed/assigned
* With the help of various reports from internal and external resources (ie.
reporting workbench) assesses patient needs for outreach and makes plan on best action to take to close the gap in their care as needed or directed
* Performs and documents outreach efforts to patients following NeighborHealth protocols to connect them to care with the goal of improving their health.
* Navigates EPIC to access relevant and appropriate information according to guideline when needed
* Handles calls appropriately
* Utilizes problem solving skills
* Schedules, re-schedules and cancels appointments
* Documents clear and concise messages and routes appropriately
* Manages refill requests and encounters accurately and effectively, according to guidelines.
* Knowledgeable of My Chart and patient access workflows
* Knowledge of “red flag”/ urgent symptoms: know when immediate nurse involvement is needed.
* Provide...
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Type: Permanent Location: East Boston, US-MA
Salary / Rate: Not Specified
Posted: 2025-06-04 08:39:30
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EMS/OHS/QMS Third Party Auditor - Remote- Quebec
Intertek is searching for an EMS/OHS/QMS Third Party Auditor to join our Business Assurance team in our Quebec, Canada.
This is a fantastic opportunity to grow a versatile career in Management System Auditing!
What you’ll do:
* Follow Intertek's Compliance Code, Policies and Procedures
* Represent the audit team and Intertek to clients
* Develop Audit Plans
* Plan and coordinate travel plans for audits as applicable
* Evaluate clients' management systems through documentation review, on-site observation, and interviews
* Identify and document areas of conformance and nonconformance
* Write Comprehensive reports and recommendations based on audit findings
* Evaluate and approve client corrective actions
* Submit time and expense reports on time, for approval
* Train, mentor, and witness (as part of the auditor qualification process) audit teammates if requested.
· What it takes to be successful in this role:
* Education and advanced course work, training and experience in environmental, safety and quality management required.
* 5+ years of professional experience in industry
* Knowledge of principles and practices of manufacturing systems
* Knowledge of EMS/OHS laws and regulations
* Experience in implementation of and/or auditing ISO management systems
* Ability to travel 75% of the time by plane or car
* Valid driver’s license and reliable driving record (required)
* Must have ISO 9001, ISO 14001, or ISO 45001 Lead Auditor Training
* 3rd Party Auditing experience preferred
* This is a remote position; however, applicants must reside in and be able to legally work in Canada.
Physical Requirements:
* Ability to communicate and interact effectively in both verbal and written format.
* Ability to view, read and comprehend a variety of reports and manuals of a technical nature, computer screen, etc.
* Physical dexterity to perform assessment functions which are inherent to the position, such as investigating all areas of client facilities which requires bending/stooping, reaching, climbing, etc.
* Mobility to travel by auto and airplane.
* Ability to be on your feet, walking, for typical full shifts of 6 - 8 hours.
* Exposure to various industrial environments.
* The ability to ascend or descend ladders, stairs, scaffolding, ramps, poles and the like, using feet and legs and/or hands and arms.
* The ability to express or exchange ideas by means of the spoken word.
Must be able to convey detailed or important spoken instructions to other workers accurately, loudly, or quickly.
* The ability to perceive the nature of sounds at normal speaking levels with or without correction.
Ability to receive detailed information through oral communication, and to make the discriminations in sound.
* The ability to exert up to 10 pounds of force occasio...
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Type: Permanent Location: Quebec, CA-QC
Salary / Rate: Not Specified
Posted: 2025-06-04 08:39:07
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The Capabilities, Analysis and Development (CAD) division of Applied Research Associates, Inc.
(ARA) has an outstanding opportunity for an exceptional Materials Scientist/Engineer with experience in manufacturing/production systems.
As part of the Counter-WMD Analysis Cell (CWAC), our tightly-knit and highly-focused team conducts detailed technical analyses of foreign, WMD-related industrial facilities, processes, and equipment using multiple intelligence sources, analytical tools, and engineering know-how.
We also support a multi-disciplined team that performs Research & Development on technological applications for detecting, identifying, characterizing, modeling, and defeating WMD threats to support tactical and strategic planning efforts.
In short, our CWAC team provides direct support to elements of the Intelligence Community, Combatant Command planning staffs, and operational units tasked with solving the most difficult problems involving the most dangerous weapons threatening the United States and its allies.
The work is challenging, dynamic, relevant, and important to the security of the country.
Essential Functions:
* Identify and characterize critical design elements of WMD-related facilities, processes, systems, and equipment
* Integrate an understanding of material properties, mechanical systems, and industrial production processes to identify design flaws, capability limits, and potential failure mechanisms
* Plan, conduct, and identify opportunities for research & development in support of counter-WMD, full-dimensional defeat technologies
* Support exercises that test and/or demonstrate new technologies, methodologies, and analytical tools that are under development
* Produce clearly-written technical analyses and briefings at levels comprehensible to an audience ranging anywhere from the layperson, to senior-level government representatives, to subject matter experts
* Share expertise with junior counterparts
Required Skills:
* Master’s degree or higher in Materials Science, Materials or Mechanical Engineering, or equivalent degree
* 8+ years of experience solving engineering problems
* Must be a US Citizen
* Practical materials science and mechanical systems knowledge gained through design, manufacturing, or other work experience
* Demonstrated ability to work effectively within or lead a team of peers, as well as excellent interpersonal and communications skills
* Willingness and ability to learn and grow into new areas of technical expertise outside of one’s original field
* Expert knowledge and use of Microsoft Word, Excel, and PowerPoint
* An active TOP SECRET clearance and ability to pass a Counter-Intelligence polygraph is required
Preferred Skills:
* Direct experience supporting reverse engineering, threat analysis, and vulnerability/survivability assessments of WMD-related facilities, processes, and infrastructure (to include underground f...
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Type: Permanent Location: Reston, US-VA
Salary / Rate: Not Specified
Posted: 2025-06-04 08:37:55
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The Capital Area Division (CAD) Applied Research Associates, Inc.
(ARA) is seeking a Fluid Dynamics Subject Matter Expert to be an expert with Computational Fluid Dynamics (CFD) codes such as ANSYS ®, LS-DYNA®, CFX ®, FLUENT ®. The position develops in-depth technical assessments and models of utilities for WMD facilities using multiple intelligence sources and analytical tools.
The successful candidate will perform research and development in advancing models of processes associated with the production of WMD materials and the processes associated with operation of WMD facilities.
The goal of the research is to support investigations into the behavior of those processes and advance investigations into the vulnerabilities of those processes.
The position requires providing technical Reachback support to operational planners to support tactical and strategic planning.
The position also provides occasional training to share expertise with junior counterparts and supports exercises to test new methodologies and analytical tools that are under development.
Required Qualifications:
* Master's degree in Mechanical Engineering or similar.
* Demonstrated ability to work effectively within or lead a team of peers, as well as excellent interpersonal and communications skills.
* Ability to communicate highly technical analyses at a level comprehensible to laymen and senior-level government representatives.
* Ability to clearly express in writing technical analysis results and site characterizations.
* Expertise with ANSYS ®, LS-DYNA®, CFX ®, FLUENT ®.
* 6 - 8 years of experience in solving DoD engineering/science problems.
* Practical experience in mechanical engineering structural modeling or fluid modeling.
* Direct experience supporting reverse engineering, threat analysis and vulnerability assessments of WMD-related facilities, processes and infrastructure (to include underground facilities).
* Expert knowledge and use of Word, Excel and PowerPoint.
* Modeling and simulation expertise with weaponeering and engineering analysis tools or similar.
* Research and Development of new tools and methodologies to understand and reverse engineer processes and support systems at remote WMD-related facilities.
* TS clearance with eligibility for SCI based upon a SSBI in the last five years.
Desired Qualifications:
* D degree in Engineering or Physics.
* 10 years of experience in solving DoD engineering/science problems.
* Military or defense-related experience and an understanding of operational planning and functional defeat of hard targets and underground facilities.
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employ...
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Type: Permanent Location: Reston, US-VA
Salary / Rate: Not Specified
Posted: 2025-06-04 08:37:55
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The Capabilities, Analysis and Development (CAD) division of Applied Research Associates, Inc.
(ARA) is seeking a Chemical Subject Matter Expert The position provides in-depth technical assessments of technologies emerging for chemical weapons of mass destruction.
The successful candidate will perform research and development in advancing chemistry associated the identification and extraction of trace chemicals associated with the production of chemical WMD materials and the processes in addition to identification and extraction of chemicals associated with commercial industrial processes.
The position also provides occasional training to share expertise with junior counterparts and supports exercises to test new methodologies and analytical tools that are under development.
Required Qualifications:
* Master's degree in Chemistry, Chemical Engineering or similar
* 8-10 years of experience in solving DoD engineering/science problems
* Demonstrated ability to work effectively within or lead a team of peers, as well as excellent interpersonal and communications skills
* Ability to communicate highly technical analyses at a level comprehensible to laymen and senior-level government representatives
* Ability to clearly express in writing technical analysis results
* Practical experience in chemical sciences
* Direct experience supporting characterization of chemical WMD processes
* Expert knowledge and use of Word, Excel and PowerPoint
* Research and Development of new tools and methodologies to understand and reverse engineer processes and support systems at remote WMD-related facilities
* TS clearance with SCI eligibility
Desired Qualifications:
* D degree in Chemistry.
* 5+ years of experience in solving DoD engineering/science problems.
* Military or defense-related experience and an understanding of operational planning and functional defeat of hard targets and underground facilities.
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employs over 1200 professionals.
ARA offices throughout the United States and Canada provide a broad range of technical expertise in defense technologies, civil technologies, computer software and simulation, systems analysis, environmental technologies, and testing and measurement.
The corporation also provides sophisticated technical products for environmental site characterization, pavement analysis, and robotics.
At ARA, employees are our greatest assets.
The corporation realizes that employee ownership fosters greater creativity and initiative along with higher performance and customer satisfaction levels.
ARA gives its employees the tools, training, and opportunities to take more active ro...
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Type: Permanent Location: Alexandria, US-VA
Salary / Rate: Not Specified
Posted: 2025-06-04 08:37:49
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About the Company
Vantage Group Holdings Ltd.
(Vantage) was established in late 2020 as a re/insurance partner designed for the future.
Driven by relentless curiosity, our team of trusted experts provides a fresh perspective on our clients’ risks.
We add creativity to tech-enabled efficiency and robust analytics to address risks others avoid.
Vantage provides specialty re/insurance through its operating subsidiaries in Bermuda and the U.S.
Vantage has approximately 340 colleagues in both the United States and Bermuda. We have offices in Chicago, IL, Norwalk, CT, Alexandria, VA, Boston, MA, New York, NY and Hamilton, Bermuda.
Additionally, we are a highly geographically diverse workforce with colleagues based in 25 states and counting.
We fully support work flexibility including remote and hybrid work arrangements.
About the role
At Vantage, the Pricing Actuary will play a critical role in building out the pricing function for the US Healthcare business unit.
Our US Healthcare business unit writes coverages across multiple lines, including medical professional liability (i.e., hospitals, facilities, Long-Term Care, physicians), general liability, and auto liability.
You will work with an established team of underwriters with vast industry experience supporting various functions, including large account pricing, model development, industry analysis, rate filing, and portfolio analysis.
You will also be part of a growing organization tasked with building and delivering data insights for our business customers and clients that help them better understand, quantify, and manage their risks differently.
We are seeking an energetic, creative, and self-motivated individual with a passion for advancing actuarial science with data and analytics.
This position will report to the Senior Pricing Actuary of US Healthcare and be a key member of the Insurance Pricing team.
We are flexible regarding location, with both remote and in-office options available.
Regardless of location, occasional travel will be required.
The base salary expectation for this role is between $140,000 and $190,000.
The actual base salary for the selected candidate may be higher, commensurate with the candidate's experience and expectations.
Additionally, Vantage offers its colleagues performance-based bonus potential, strong health and welfare benefits, retirement plans with company match, competitive time off plans, a highly flexible work environment, and much more.
Responsibilities & Accountabilities
* Assist with building and maintaining pricing models to support the US Healthcare business unit.
* Engage with the underwriting team to price large accounts.
* Perform other actuarial services, including, but not limited to, assisting with building aggregate loss distribution templates, competitor research, performing profitability and rate adequacy studies, rate filing support, and reinsurance support.
* Find innovative and creative ways to leverage da...
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Type: Permanent Location: New York, US-NY
Salary / Rate: 165000
Posted: 2025-06-04 08:33:27
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Nature of Work: Under the direction of the designated supervisor, the Volunteer Program Specialist focuses on managing volunteer onboarding, offering coaching and guidance, and tracking volunteer progress to enhance their experience and impact.
Ideal for candidates with foundational experience in volunteer management, this role provides an opportunity to develop leadership skills in volunteer coordination, program development, and strategic engagement.
Hourly Rate: $19.63
Essential Duties:
* Foster long-term volunteer relationships and provide tailored support.
* Oversee onboarding and progress tracking for independent and skill-based volunteers.
* Coordinate corporate and group events to maximize engagement.
* Collaborate closely with the Volunteer Engagement team to ensure seamless operations.
* Execute volunteer recognition programs, including appreciation events and communications.
* Attend events/meetings with volunteers all over town with tools and equipment, and pick up waste materials to take down to the Wheeler Service Center
* Perform other duties as assigned.
Required Qualifications:
* Must obtain CPR/AED and First Aid certification within 30 days of employment.
The City offers CPR/AED and First Aid classes, which are free to Parks employees.
Please note, your certification must be from an organization that has been approved by the Bureau of Community and Health Systems, Child Care Licensing Division.
Please see following link for list of approved organizations: https://www.michigan.gov/lara/0,4601,7-154-89334_63294_5529_49572_49583-82382--,00.html.
* Must have a valid driver’s license.
* Experience in volunteer coordination or training.
Preferred Qualifications:
* Familiarity with parks and recreation operations, including community outreach.
* Knowledge of and experience with volunteer management best practices, including recruitment, training, and retention strategies.
* Experience tracking and analyzing program data to assess effectiveness and recommend improvements.
* Bachelor’s degree in Public Administration, Parks Management, or a related field.
* Demonstrated ability to lead small teams or coordinate multiple stakeholders.
Physical Requirements: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential duties of this job.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.
Positions in this class typically require: driving, walking, standing, reaching, lifting, pushing, pulling, grasping, talking, hearing, seeing and repetitive motions.
Move and lift light objects up to 50 lbs.
such as mail, files, event signs, supplies and tables.
Set up and take down a table up to 50 lbs.
without assistance on most occasions.
Will work alone on most occasions for events.
Operating office equipment requiring conti...
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Type: Permanent Location: Ann Arbor, US-MI
Salary / Rate: Not Specified
Posted: 2025-06-04 08:32:35
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Nature of Work: Under the direction of the designated supervisor, the Volunteer Support Specialist provides foundational support for volunteer programs, focusing on volunteer onboarding, implementing events, and community engagement.
This position is ideal for entry-level candidates seeking to grow their experience in volunteer management, event execution, and volunteer appreciation initiatives.
Hourly Rate: $18.68
Essential Duties:
* Assist in coordinating events and logistics.
* Provide on-site orientation for volunteers, ensuring clarity of roles and adherence to safety protocols during events.
* Track volunteer participation and event outcomes, maintaining accurate records.
* Serve as a point of contact for volunteers during events.
* Ensure volunteers feel appreciated during events through recognition and support.
* Collaborate with team members to refine event processes and enhance volunteer experiences.
* Promote the volunteer program at community events to increase engagement and visibility.
* Attend events/meetings with volunteers all over town with tools and equipment, and pick up waste materials to take down to the Wheeler Service Center
* Perform other duties as assigned.
Required Qualifications:
* Must obtain CPR/AED and First Aid certification within 30 days of employment.
The City offers CPR/AED and First Aid classes, which are free to Parks employees.
Please note, your certification must be from an organization that has been approved by the Bureau of Community and Health Systems, Child Care Licensing Division.
Please see following link for list of approved organizations: https://www.michigan.gov/lara/0,4601,7-154-89334_63294_5529_49572_49583-82382--,00.html.
* Must have a valid driver’s license
* Strong organizational skills and attention to detail.
* Ability to work collaboratively and communicate effectively.
Preferred Qualifications:
* Experience with event coordination, volunteer recruitment, or assisting with group activities.
* Knowledge of basic safety protocols and procedures for volunteer activities.
* Experience using volunteer management platforms or basic databases.
* Strong interpersonal skills to interact effectively with diverse groups.
* Strong organizational skills and attention to detail.
* Ability to work both independently and collaboratively as part of a team.
Physical Requirements: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential duties of this job.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.
Positions in this class typically require: driving, walking, standing, reaching, lifting, pushing, pulling, grasping, talking, hearing, seeing and repetitive motions.
Move and lift light objects up to 50 lbs.
such as mail, files, event signs, supplies and tables.
...
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Type: Permanent Location: Ann Arbor, US-MI
Salary / Rate: Not Specified
Posted: 2025-06-04 08:32:33
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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:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Als führendes Unternehmen in der Gesundheitsbranche bieten wir motivierten und talentierten Lernenden die Chance, ihr Potenzial zu entfalten und wertvolle Erfahrungen in einem innovativen und dynamischen Umfeld zu sammeln.
Unser Lernendenprogramm bietet eine vielfältige Palette an Möglichkeiten wie z.
B.
in einem globalen Netzwerk von Expert:innen zu arbeiten oder an innovativen Projekten mitzuwirken.
Wir legen Wert auf Vielfalt, Inklusion und persönliches Wachstum und bieten eine unterstützende und inspirierende Arbeitsumgebung.
Bewirb dich noch heute, um Teil einer dynamischen Unternehmung zu werden.
Standort:
Die Cilag AG in Schaffhausen wurde 1936 gegründet und ist seit 1959 Teil von Johnson & Johnson.
Der Standort fungiert als einer der wichtigsten Produzenten der Schweizer Pharmaindustrie und als bedeutender Arbeitgeber in der Region Schaffhausen.
Das Unternehmen stellt hochwertige pharmazeutische Substanzen und Produkte her, die Patienten auf der ganzen Welt zugutekommen.
Wir suchen DICH – Lehrstelle Logistiker:in EFZ 2026
Ausbildungsdauer:
3 Jahre
Abschluss:
Eidgenössisches Fähigkeitszeugnis Logistiker:in EFZ
Vorbildung:
Obligatorische Schule mit Grundanforderungen abgeschlossen
Ausbildungsort:
Diverse Standorte im Raum Schaffhausen
Hauptsitz: Cilag AG, Hochstrasse 201, 8200 Schaffhausen
Was du bei uns lernst:
Logistiker:innen transportieren, lagern und verteilen Güter fachgerecht.
Bei uns arbeitest du in verschiedenen Lagern in einem Produktionsbetrieb.
Mit der Fachrichtung Lager bis du für die fachgerechte Bewirtschaftung von Waren zuständig.
Du nimmst diese in Empfang und kontrollierst und verbuchst sie anschliessend im Computersystem.
Mit Gabelstaplern oder komplexen Fördersystemen lagerst du die Güter in geeigneter Weise ein.
Wenn eine Bestellung eintrifft, kannst du die entsprechenden Waren für die Auslieferung oder den Versand vorbereiten, verpacken und beschriften.
Du wirst lernen die Lieferpapiere zu erstellen und die Fahrzeuge auf fachgerechte und sichere Art und Weise zu beladen.
Was du mitbringen solltest:
- Praktisches Verständnis
- Handwerkliches Geschick
- Organisationstalent
- Selbstständigkeit
- Zuverlässigkeit und Verantwortungsbewusstsein
- Ausdauer und Konzentrat...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-06-04 08:31:17
-
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:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Als führendes Unternehmen in der Gesundheitsbranche bieten wir motivierten und talentierten Lernenden die Chance, ihr Potenzial zu entfalten und wertvolle Erfahrungen in einem innovativen und dynamischen Umfeld zu sammeln.
Unser Lernendenprogramm bietet eine vielfältige Palette an Möglichkeiten wie z.
B.
in einem globalen Netzwerk von Expert:innen zu arbeiten oder an innovativen Projekten mitzuwirken.
Wir legen Wert auf Vielfalt, Inklusion und persönliches Wachstum und bieten eine unterstützende und inspirierende Arbeitsumgebung.
Bewirb dich noch heute, um Teil einer dynamischen Unternehmung zu werden.
Standort:
Die Cilag AG in Schaffhausen wurde 1936 gegründet und ist seit 1959 Teil von Johnson & Johnson.
Der Standort fungiert als einer der wichtigsten Produzenten der Schweizer Pharmaindustrie und als bedeutender Arbeitgeber in der Region Schaffhausen.
Das Unternehmen stellt hochwertige pharmazeutische Substanzen und Produkte her, die Patienten auf der ganzen Welt zugutekommen.
Wir suchen DICH – Lehrstelle Chemie- und Pharmatechnologe:login EFZ 2026
Ausbildungsdauer:
3 Jahre
Abschluss:
Eidgenössisches Fähigkeitszeugnis Chemie- und Pharmatechnologe:login EFZ
Vorbildung:
Obligatorische Schule mit Grundanforderungen abgeschlossen
Ausbildungsort:
Cilag AG, Hochstrasse 201, 8200 Schaffhausen
Was du bei uns lernst:
Als Chemie- und Pharmatechnologe:login (CPT) stellst du mit automatisierten Fabrikationsanlagen chemische, biologische und pharmazeutische Produkte her.
Du bist verantwortlich für die Vorbereitung, Durchführung und Kontrolle des Produktionsprozesses.
Für die Produktionsprozesse planst und berechnest du die benötigten Mengen Rohstoffe und stellst diese entsprechend bereit.
Die Vorbereitung der Anlagen, bevor die Produktion gestartet werden kann, gehört ebenfalls zu deinen Aufgaben.
Mit einer Herstellvorschrift führst du die nötigen Arbeitsschritte sicher durch.
In bestimmten Prozessphasen ziehst du Produktmuster und analysierst diese im Labor.
Nach beendeter Produktion reinigst du die verwendeten Anlagenteile und führst anschliessend Funktionskontrollen, sowie kleinere Wartungsarbeiten durch.
Was du mitbringen solltest:
- Interesse an Mathematik, Chemie, Physik
- Handwerkliches Geschick
- T...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-06-04 08:31:17
-
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 Control
Job Category:
Professional
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
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 QC Analyst to be in Ringaskiddy.
An pre-identified candidate for consideration has been identified.
However, all applications will be considered.
Purpose:
Performs advanced tests and analyses to assure that products align with established specifications.
Carries out complex calculations and documents test results.
This is a volume driven position that that directly touches product.
Compiles and analyzes data on reoccurring product defects to determine root cause.
Documents analysis results.
Analyzes raw material inspection logs for consistent failures.
Notifies purchasing and quality departments about suppliers that have provided inferior products.
Studies work processes, measurements and performance metrics to identify improvement areas.
Recommends new or modified procedures based on findings.
Collaborates with customers, suppliers and associates to define and improve quality standards and expectations.
Participates on process improvement teams.
Monitors and scrutinizes internal and external complaints and compiles data to be used in reports.
Performs analyses in order to achieve compliance with specifications using a wide variety of chemical, biological and physical standard procedures.
You will be responsible for:
* Attending daily meetings, working on own initiative.
* Testing and reviewing daily
* Training new analysts
* Always aim to meet site metrics
* Promoting 6S within the laboratories
Qualifications / Requirements:
Education:
A minimum of a bachelor’s degree in a science related discipline and 3 years of experience in a pharma company.
Experience and Skills:
* Experience in lab-based testing
* Proficient in Lab report writing.
We would love to hear from you!#RPOAMS
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-06-04 08:31:15
-
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:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Als führendes Unternehmen in der Gesundheitsbranche bieten wir motivierten und talentierten Lernenden die Chance, ihr Potenzial zu entfalten und wertvolle Erfahrungen in einem innovativen und dynamischen Umfeld zu sammeln.
Unser Lernendenprogramm bietet eine vielfältige Palette an Möglichkeiten wie z.
B.
in einem globalen Netzwerk von Expert:innen zu arbeiten oder an innovativen Projekten mitzuwirken.
Wir legen Wert auf Vielfalt, Inklusion und persönliches Wachstum und bieten eine unterstützende und inspirierende Arbeitsumgebung.
Bewirb dich noch heute, um Teil einer dynamischen Unternehmung zu werden.
Standort:
Die Cilag AG in Schaffhausen wurde 1936 gegründet und ist seit 1959 Teil von Johnson & Johnson.
Der Standort fungiert als einer der wichtigsten Produzenten der Schweizer Pharmaindustrie und als bedeutender Arbeitgeber in der Region Schaffhausen.
Das Unternehmen stellt hochwertige pharmazeutische Substanzen und Produkte her, die Patienten auf der ganzen Welt zugutekommen.
Wir suchen DICH – Lehrstelle Laborant:in EFZ Fachrichtung Biologie 2026
Ausbildungsdauer:
3 Jahre
Abschluss:
Eidgenössisches Fähigkeitszeugnis Laborant:in EFZ Fachrichtung Biologie
Vorbildung:
Obligatorische Schule mit Grundanforderungen abgeschlossen
Ausbildungsort:
Cilag AG, Hochstrasse 201, 8200 Schaffhausen
Was du bei uns lernst:
Laborant:innen arbeiten in der Forschung, Entwicklung, Produktion, Kontrolle oder in der Diagnostik.
Sie planen und führen Versuche durch, überwachen deren Verlauf und erstellen Auswertungen.
Mit Fachrichtung Biologie untersuchst du Organismen, deren Aufbau und Entwicklung sowie ihre Wechselwirkung mit Wirkstoffen.
Dabei arbeitest du mit Mikroorganismen, Zellen und Pflanzen.
Du hilfst mit, die Art und Funktionsweise lebender Systeme auf verschiedenen Stufen zu ergründen: als ganze Organismen, in Zellkulturen, an isolierten Organen oder anhand isolierter Zellbestandteile und Biomoleküle.
Du arbeitest mit Messgeräten und verschiedenen Apparaturen und führst diverse Berechnungen durch.
Du beurteilst den Versuchsablauf und hältst die Vorschriften zur Arbeitssicherheit, zum Umweltschutz und zur Qualitätssicherung ein.
Was du mitbringen solltest:
- Gute Leistungen in den naturwissenschaftlichen und...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-06-04 08:31:12
-
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 Control
Job Category:
Professional
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
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 Analyst Quality Control to be in Cork.
An pre-identified candidate for consideration has been identified.
However, all applications will be considered.
You will be responsible for:
* Achieves competency in laboratory methods and procedures.
* Trains other QC analysts in laboratory methods and procedures when required.
* Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
* Executes validation, operation, maintenance, calibration and troubleshooting of equipment and its associated software.
* Writes, executes, reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
* Performs routine and non-routine analytical testing activities.
* Review and approval (where appropriate) of laboratory test results.
Ensures that testing and results approval are completed within agreed turnaround times.
* Writes and reviews laboratory TMs, SOPs, TMDs and WIs as directed by company policy.
* Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
* Is an active member of the QC group and provide assistance with other group activities as required and communicates relevant issues to the QC Specialist, QC Team Leader and Manager.
* Deals with Quality Issues in an accurate and timely manner.
* Maintains and develops knowledge of analytical technology as well as cGMP standards.
* In process control testing and activities to support the production units.
Qualifications / Requirements:
* A third level qualification of a scientific/technical discipline is required.
* Knowledgeable of FDA/EMEA regulatory re...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-06-04 08:31:09
-
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:
Adelaide, South Australia, Australia, Eight Mile Plains, Queensland, Australia, North Ryde, New South Wales, Australia, Notting Hill,, Victoria, Australia, Osbourne Park, Western Australia, Australia
Job Description:
* Great Place to Work® Certified - 2024
* Competitive salary package, flexible work practices, award winning benefits
* Continuous training and development
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
THE OPPORTUNITY
An opportunity is now available for a Senior Clinical Project Manager/Lead Local Trial Manager to join our high performing Global Clinical Operations (GCO) team.
The Lead, Local Trial Manager plays a crucial role in overseeing the local management of clinical trials within Australia.
You will be your global project team’s local point of contact and will provide local project team oversight to achieve flawless execution of your assigned clinical trials.
You will work closely with your Manager, Clinical Operations, however you will remain responsible for the conduct of your projects.
You will cover all aspects of study execution from feasibility and pre-trial assessment through to database lock and close-out activities.
The role extends more broadly to include, in some cases, leading a cross functional team or working on early development pipeline products.
As an exceptional leader, you will build strong working relationships with internal and external customers and ensure the smooth running of our trials; delivering them on time, on budget and in accordance with Good Clinical Practice (GCP), relevant SOPs and regulatory requirements.
In addition, you will be required to contribute to process improvement as well as training and mentoring other team members.
The is a permanent, full-time role.
RESPONSIBILITIES
* Lead country protocol and site feasibility assessments in collaboration with relevant stakeholders, ensuring adherence to local...
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Type: Permanent Location: North Ryde, AU-NSW
Salary / Rate: Not Specified
Posted: 2025-06-04 08:31:04
-
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:
Scientific/Technology
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
The Programmer is an experienced clinical trial programmer with in-depth knowledge in industry standard and complex data structures, programming languages, and/or reporting solutions with proven technical capabilities in leading clinical trial activities and/or teams in accordance with departmental processes and procedures.
The position is responsible for oversight or the development of one or more clinical data management trial activities of moderate to high complexity/criticality. Including data model specifications, data stream integrations and transformation of source to internal data models and/or CDISC submission ready SDTM tabulation packages (aCRF, define.xml, cSDRG, etc). Creates and executes edit check programs, listings and report solutions to aid in monitoring of safety, risk, compliance and ensures quality data review.
Performs reporting solutions role creating study-specific reports translating clinical study team needs into specifications aggregating clinical data sources into custom data and report to monitor safety, risk and compliance.
* Accountable for one or more clinical programming trial activities of moderate to high complexity, scope and/or criticality.
* Performs comprehensive review of, and provides input into, project requirements and documentation. Identifies gaps, proposes solutions and applies expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.
* Ensures latest standards are being utilized, current technologies are deployed.
* Create and/or review specifications for mapping internal data review model for fit for purpose reporting and/or as well as submission ready CDISC SDTM.
Design mapping algorithms for nonstandard conversions.
* Responsible for creation or review of internal data model for fit for purpose reporting consumption and/or submission ready CDISC SDTM packages for health authority submissions and keeping abreast in changing regulatory requirements. Program, or oversight of quality review checks, study specific reports for use by team members and consumers of data.
* May perform role that programmatically aggregates clinical data sources into custom ...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-06-04 08:30:54
-
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 Mechanical Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
San Jose, California, United States of America, Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is recruiting for a Sr.
Quality Engineer, located in Santa Clara, California.
This is a fully onsite position.
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/.
Our Design and Sustaining Quality team advances the MONARCH™ surgical robotics platform by providing quality engineering support and leadership for design of new products and design changes for commercial products.
We collaborate on breakthrough medical technologies that unite multiple subject areas to improve patient outcomes and advance medical professionals’ skills.
Key Responsibilities:
* Support product requirements, risk management, verification strategies, validation strategies, and quality audits.
* Collaborate on, review, and approve design, manufacturing, quality, engineering, and validation / qualification documentation.
* Collaborate cross-functionally with, including but not limited to, Quality, R&D, Supply Chain (including Manufacturing), Regulatory Affairs, Marketing, Clinical Affairs/Research.
* Develop, revise, and apply quality system procedures.
* Drive prevention and detection of defects at earliest phase of product design, continuous improvement, and customer satisfaction.
* Investigate and resolve product and quality system nonconformances.
* Provide recommendations on statistical analysis and analytical problem solving for product development.
* Lead and execute design and quality projects.
* Ensure compliance with GMP (Good Manufacturing Practices), ISO (International Organization for Standardization) and other applicable standards and regulations.
* Guide contractor personnel in achieving deliverables.
Qualifica...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-04 08:30:46
-
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:
Scientific/Technology
All Job Posting Locations:
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
Johnson & Johnson Innovative Medicine is hiring a Senior Scientist, Biostatistics to be located in either Raritan, NJ, Titusville, NJ, Spring House, PA, or San Diego, CA.
The Senior Scientist, Biostatistics will support the Oncology Therapeutic Area with a focus on: solid tumors or hematologic malignancies; cancer interception with the goal of developing products that interrupt the carcinogenic process; biomarkers that may help guide targeted, individualized use of our therapies; as well as safe and effective identification and treatment of early changes in the tumor microenvironment.
Key Responsibilities:
* Provide statistical input into the clinical development of drugs for treatment of cancer.
* Work with the clinical team in designing clinical studies, leading/authoring the statistical analysis plan, conducting the statistical analysis, and providing statistical input to the clinical study report.
* Provide input in the preparation of scientific presentations and manuscripts.
* Participate in process improvement, training, standards development and enhancing statistical technical expertise.
* Liaise with other statisticians within the organization, building working relationships with therapeutic area leaders, internal SAS programmers, clinical trial managers, and personnel from regulatory affairs, medical writing, and other disciplines as needed.
Qualifications
Education:
A Ph D in Statistics or related field, OR a Master’s Degree with at least six (6) years of clinical data analysis experience, is required.
Experience and Skills Required:
* Working knowledge of statistical software suc...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-04 08:30:39
-
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/Medical Operations
Job Category:
Professional
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Irvine, California, United States of America, New Brunswick, New Jersey, United States of America, Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, San Jose, California, United States of America, Warsaw, Indiana, United States of America
Job Description:
We are searching for the best talent for a Manager, Global Clinical Evaluation to join our MedTech Surgery Team.
This is a remote position based in the United States.
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 surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world.
Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer.
Patients are waiting.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Purpose:
The Manager, Global Clinical Evaluation provides leadership, motivation, and strategic direction for the general technical writing activities for the generation of Clinical Evaluation Reports/Plans (CER) and Summary of Safety and Clinical Performance Reports (SSCP) for their assigned therapeutic area within J&J MedTech Surgery.
They also support broader initiatives and cross-platform activities to support the continuous process improvement activities of the Global Clinical Evaluation Team.
You will be responsible for :
* Provides oversight and guidance to resources on compliant document execution and generation
* Manages relationships and contracting with external vendors for generation of documents supporting these processes
* Develops strategic plans to ensure operating company deliverable timelines are met, and practices are being consistently deployed across the global organization
* In conjunction with the leadership team, designs, develops and leads workshops to define processes globally and keeps abreast of regulatory requi...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-06-04 08:30:37
-
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 – Specialty Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Norderstedt, Schleswig-Holstein, Germany
Job Description:
Interne Stellenausschreibung vom 02.06.2025 bis 16.06.2025
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/
Johnson & Johnson Electrophysiology
Mit diesem Geschäftsbereich 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
Johnson & Johnson Electrophysiology 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 ab dem 01.10.2025 eine
Associate Clinical Consultant (d/m/w) im Außendienst
Trainee Sales Consultancy – Johnson &...
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Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-06-04 08:30:35
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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:
Procurement
Job Sub Function:
Category
Job Category:
People Leader
All Job Posting Locations:
Cambridge, Massachusetts, 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
We are searching for the best talent for an Associate Director, Viral Vectors (Cell and Genetic Medicines Discovery) that will be based in Cambridge, MA.
Purpose:
We are seeking an experienced and dynamic Associate Director to join our cell therapy discovery efforts and build a dedicated team in Cambridge, MA.
In this role, you will leverage your expertise in viral vector technology to drive innovative therapeutic solutions for advancing cell therapies.
This position presents a unique opportunity to contribute to groundbreaking research in CAR-T cell therapy.
If you are passionate about advancing scientific discovery and possess a collaborative mindset, we invite you to apply!
Key Responsibilities:
* Establish, build, and mentor a high-performing team dedicated to the design and screening of viral vectors for CAR-T therapies.
* Leverage extensive knowledge of cell targeting approaches combined with lentivirus vector engineering, production, analytics, and in vitro screening/testing to guide the team’s discovery, research, and development efforts.
* Provide leadership in the development of our cell therapy platform and pipeline, overseeing projects related to viral vector preparation, quantitation, and characterization. Support the implementation of in vitro functional assays such as multi-color flow cytometry, ELISA, cytotoxic assays, and vector copy number (VCN) analysis.
* Help build and establish laboratory facilities to support relevant workstreams
* Interpret experimental data, summarize and report findings to project teams. Communicate complex technical concepts clearly to a variety of stakeholders, including senior management.
* Identify and conceptualize new ideas; design, plan, and lead experiments while prioritizing areas of focus based on business ...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2025-06-04 08:30:33
-
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:
Biological Research
Job Category:
Scientific/Technology
All Job Posting Locations:
Cambridge, Massachusetts, 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
We are searching for the best talent for two Senior Scientist, Viral Vectors (Cell and Genetic Medicines Discovery) that will be based in Cambridge, MA.
Purpose:
We are seeking a highly motivated and experienced scientist to join our CAR-T cell therapy discovery efforts as a Senior Scientist.
In this role, you will play a key part in advancing our research initiatives by leveraging your expertise in viral vectors and molecular biology. This position presents a unique opportunity to contribute to groundbreaking research in CAR-T cell therapy.
If you are passionate about advancing scientific discovery and possess a collaborative mindset, we invite you to apply!
Responsibilities:
* Utilize your extensive knowledge in vector engineering, virology, and molecular biology to contribute meaningfully to our cell therapy platform and pipeline development.
* Conduct vector screening, optimize vector packaging and production, and perform analytical quantification of viral vector particles using relevant assessments including protein and PCR-based assays, particle potency testing via flow cytometry, and vector copy number (VCN) analysis.
* Contribute to optimization efforts focused on increasing viral titers and purity to enhance the overall efficiency of production processes.
* Support the development of innovative vector analytical and characterization assays.
* Collaborate closely with cross-functional teams to test different designs, ensuring the delivery of reliable and consistent data.
Present data to research and cross-functional teams.
* Stay informed about industry developments, continuously learn, and thrive in a fast-paced team environment.
* Deliver results in alignment with project timelines while maintaini...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2025-06-04 08:30:33
