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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: Engineering Intern
As an Engineering Intern, you will be part of the Engineering team to deliver a technical project for process improvement.
Your Responsibilities:
* Understand the manufacturing environment and how to collaborate with different stakeholders to solve problems
* Work within cross-functional teams to build vendor relationships and new process capability implementation
* Data visualization tool creation/usage and documentation updates
What You Need to Succeed (minimum qualifications):
* Education: Currently enrolled in an Engineering major including (but not limited to) Chemical, Mechanical, Electrical, or Process
* Experience in Microsoft Suites
* A willingness to learn
What will give you a competitive edge (preferred qualifications):
* Have an interest in animals, using data to solve problems, improving processes or working in manufacturing
* Strong communication and interpersonal skills
* Strong organizational and time management skills
* Must be able to work exceptionally well independently and with minimal supervision
Additional Information:
* Travel: 10% - to corporate facility in Greenfield, IN for opening/closing
* Location: Clinton Manufacturing Plant - Clinton, IN
Our Internship Program
Our internship program is designed to provide students with experiences! Internships are project based and comprised of business-critical needs.
All interns have the opportunity to significantly impact Elanco’s success over the summer and kickstart a career that counts.
* Internship Dates: May 19th – August 8th (12 Weeks)
* Competitive salary: $20-$40/hour (dependent upon major and year in school)
* Networking events
* Assigned mentors
* Professional development opportunities
* Optional all-inclusive housing for $150 per week or a $4000 housing stipend (ONLY for Sales and Kansas City/Elwood interns)
* Full time roles ...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-08-29 08:54:24
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Financial Business SR Analyst - Supply Chain
Job Description
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.
In this role, you will:
Reporting to the Associate Director of Enterprise Manufacturing and Logistics, the Business Analyst is expected to independently partner with values stream teams (commercial, R&D and supply chain) to provide financial, business and strategic analysis and insights.
Seeking a strategic thinker with strong leadership abilities, collaborative mindset, deep analytical skills, exceptional communication skills, and a passion for driving results.
* Conduct value stream analysis integrating inputs across commercial, manufacturing, logistics, procurement, and R&E to optimize total delivered cost and operational efficiency.
* Develop standardized ways of working and tools to rapidly provide views of total delivered cost including raw materials, conversion spend, distribution cost, etc.
* Integrate data sources and apply assumption-based modeling and scenario building to navigate ambiguity and drive actionable insights.
* Conduct unbiased financial modeling supporting Enterprise objectives and outcomes, supporting senior leadership with clear financial guidance.
* Assist with ad hoc requests from the Enterprise Value Stream leadership teams
* Written and Verbal Communication: Excellent communication and presentation skills, including strong PowerPoint / deck-writing skills; capable of catering a message appropriately for a given audience
* Structured Problem Solving: Brings structure to ambiguous problems and possesses the ability to frame key questions and develop a workplan to answer them.
* Analytical and Quantitative: Strong analytical and quantitative skills and the ability to independently generate strategic insights.
* Financial Analyses: Ability to analyze P&L trends and diagnose issues, articulate financial impact of findings/recommendations to senior leadership
* Business Judgment: Possesses insight and understanding in dealing with risks and opportunities in business that is likely to lead to favorable outcomes.
* Influence and Stakeholder Management: Ability to manage and influence senior-level stakeholders
* Change Management: Capable of understanding organizational dynamics, individual incentives, and barriers to change to implement new ways of working in line with business priorities
* Knowledge and Enthusiasm for K-C: Knowledge of the K-C organization, brands, metrics, etc.; enthusiastic about the potential strategic ...
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Type: Permanent Location: Roswell, US-GA
Salary / Rate: Not Specified
Posted: 2025-08-29 08:47:21
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program..
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Adell, Wisconsin facility and after 60 days of training, would support the New Holstein, WI and Boscobel, WI facilities.
Position would be based out of Adell.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits. Manage WPDES permits.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager.
* Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs.
* Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facilities.
Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
* Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks.
* Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations.
* Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corporate EHS department using the R...
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Type: Permanent Location: Adell, US-WI
Salary / Rate: Not Specified
Posted: 2025-08-29 08:38:57
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Liberty POST is currently seeking a motivated and energetic Early Childhood School Psychologist for per diem employment to work with children who are birth-5 years old through Early Intervention and Preschool Special Education programs.
Immediate positions are available throughout Syracuse.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994.
Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Effectively communicates and works with related agencies, community members, clients, families and co-workers.
* Establishes and maintains a rapport with clients/family members/caregivers and co-workers.
* Review client information prior to evaluation and complete necessary client forms in collaboration with family, other evaluators and current service providers.
* Complete IEP direct including goals, outcome summary and results.
* Gather outside information regarding child’s performance in a variety of settings.
* Utilize Provider Soft to record notes and evaluation results and submit evaluation write up to team leader.
* Attends and participates in ongoing staff in-services and mandatory quarterly meetings.
* Attend CPSE meetings.
Qualifications, Knowledge and Experience:
* Master’s Degree in School Psychology or Doctor of Psychology
* Evaluation and assessment experience required. Familiarity with a variety of preschool assessment tools.
* Effectively communicates via phone, e-mail, in public, and in large groups.
* Proficient on assessment tools necessary for evaluations.
* Works independently, manages time and prioritizes tasks appropriately.
* Strong organizational skills necessary
* Evidence of independence, initiative and forward thinking related to clinical expertise.
* Open to feedback and commitment to quality of provided services.
* Responds positively to suggestions/directions, maintains a flexible attitude and generates new ideas and process improvements.
* Maintains confidentiality of client records.
Benefits for this position:
* Health Benefits and Retirement packages available for FT positions
* Accrual of sick time based on NYS Sick time Laws
* Mentoring is offered to all providers
* Access to unlimited CEU courses offered that are accredited through ASHA, AOTA, APTA and CTLE
* Flexible sched...
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Type: Permanent Location: Syracuse, US-NY
Salary / Rate: Not Specified
Posted: 2025-08-29 08:37:36
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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:
Career Programs
Job Sub Function:
R&D LDP
Job Category:
Career Program
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Irvine, California, United States of America, Jacksonville, Florida, United States of America, Raynham, Massachusetts, United States of America, Santa Clara, California, United States of America, West Chester, Pennsylvania, 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
We are searching for the best talent for the Research and Development Leadership Development Program- 2026 Summer Internship.
Purpose: We offer an exciting 12-week summer engineering internship with an emphasis in Product Research and Development.
You will experience unrivaled departmental opportunities supporting a wide variety of highly specialized teams such as: New Product Development, Mechanical Design, Computational Modeling and Simulation, Materials Development, Robotics, Research and Testing, Manufacturing and Design Quality.
Not only will you have the ability to develop your engineering skills through on-the-job assignments.
You will:
* Improve your industry knowledge through open forum conversations with senior company leaders and shadowing senior engineers.
* Create or improve your personal brand through skills building workshops and internship networking events.
* Have the power to connect with and support our local towns through community activities.
You will be responsible for:
* Working in a fast-paced cross functional, technologically advanced corporate environment in an internship program focused on developing individual engineers capable of pursuing careers across medical device businesses and high-volume manufacturers.
* Learning about anatomy, disease states, and deformities and the surgical procedures and products used to address these conditions.
* Being part of a team responsible for the support of complex automated manufacturing equipment, working on the manufacturing engineering team
* Participating in machine development; equipment changes and testing protocol
* Becoming familiar with design control documentation required by regulatory gove...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-08-29 08:34:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Clinical Development & Research – Non-MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Groningen, Netherlands
Job Description:
Johnson & Johnson is currently seeking a Staff R&D Scientist for our JnJ Surgical Vision located in Groningen, Netherlands.
JnJ Surgical Vision is focused on providing the full range of advanced optical technologies and support to help eye care professionals deliver optimal vision and lifestyle experiences to patients of all ages.
AMO Groningen BV is specialized in the development, improvement and manufacturing of state of the art surgical ophthalmic products, mainly intra-ocular lenses.
The facility consists of small and integrated Research, Development and Manufacturing teams that have strong track records.
The team is expanding, and we are currently looking for a talent for the position of:
We are searching for the best talent for R&D Scientist.
Purpose: The Senior Scientist is a key addition to the IOL optics and vision science team located in Groningen, The Netherlands, Europe.
He/She will be responsible for R&D activities related to the design and development of intraocular lenses and will support the development of new optical metrology for testing intraocular lenses.
You will be responsible for:
· Participate in the development of new concepts for unique medical devices from ideation to market phase.
· Lead in design and development of new intraocular lenses and new optical metrology for testing intraocular lenses.
· Develop test methods and validation systems to characterize new and existing intraocular lenses.
· Lead requirements development, documentation of design, writing and execution of protocols and reports.
· Builds and maintains relationships with critical partners and notified bodies.
Lead expert networks and write grant proposals.
· Stay current with the status of competitive products, with cutting-edge medical device industry and with technology trends to ensure innovative product design. Investigate and evaluate existing technologies.
· Contribute to IP strategy and assess external ideation.
· Lead multi-disciplinary research teams and will be responsible for initiating and conducting independent research tasks with European res...
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Type: Permanent Location: Groningen, NL-GR
Salary / Rate: Not Specified
Posted: 2025-08-29 08:34:34
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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 Planning
Job Sub Function:
Supply Network Planning
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America, Milpitas, California, United States of America
Job Description:
We are searching for the best talent for a Global Supply Planner, in Irvine, CA!
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 outstanding talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech (https://www.jnj.com/medtech)
This individual is responsible for supply planning globally for accessories used in surgical procedures while meeting service (LIFR), inventory, Back Order, and SLOB targets.
Individual will build strong relationships and will work directly with External Manufacture Supplier(s) providing assigned products.
RESPONSIBILITIES:
As a key stakeholder in Global Sales and Operations Planning Process
- Interprets internal forecasts and provides short- and long-term forecasts to EM Supplier(s) to achieve customer service targets and inventory goals
- Issue, track and manage PO’s, along with resolving AR issues to ensure EM Supplier(s) are being paid on a timely basis
- Manage regional supply shipments from EM Suppliers
- Effectively manage phase in and phase out of product changes
- Ensure appropriate inventory levels utilizing entitlement modeling and identify and drive minimization of scrap
- Participate in monthly IBP (Integrated Business Planning) process, and prepare & present in various forums within J&J and with supplier (daily, weekly, monthly, quarterly forums)
- Collaborates with EM Supplier(s) in assessing capacity requirements to maximize output and flag shortfalls as appropriate
- Develop strong working relationships with EM Suppliers and internal cross functional teams to improve supply reliability
- Manage and proactively communicate supply status and critical supply chain metrics.
Perform ad-hoc analytical analysis, recognize issues, develop plan for resolution, and implement and / or influence the support of key partners to aid implementation
- Participate in various Global Supply Chain initiatives
QUALIFICATIONS:
- A minimum of a bachelor’s degree in a relevant discipline is required
- A minimum of 4 years of Planning and...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-08-29 08:33:12
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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: 2025-08-29 08:33:02
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
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: 2025-08-29 08:33:00
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Company
Federal Reserve Bank of Kansas City
The Economic Research Department at the Federal Reserve Bank of Kansas City is recruiting for the position of Research Associate (RA).
The Department conducts innovative analysis and research on a variety of topics, including international trade, macroeconomics, monetary policy, labor economics, fiscal policy, energy economics, regional economics, and payments.
The Department has openings for RAs to start summer 2026.
The program generally runs for 2 years with the opportunity to extend, if applicable.
This is an excellent position for someone who is passionate about research and considering a Ph.D.
in economics.
RAs develop technical skills, such as programming and working in a High-Performance Computing environment, and are exposed to a broad range of economic research topics.
Most RAs stay with the department for two to three years, at which point many return to graduate school.
RAs have gone on to Ph.D.
programs at Boston College, Columbia University, New York University, Stanford University, University of Chicago, University of Michigan, University of Minnesota, University of Wisconsin, University of Texas at Austin, University of Rochester, and Georgetown University.
Key Activities:
* Working with Ph.D.
economists on policy briefings and academic research projects.
* Gathering and analyzing data, programming economic models, and preparing charts for presentations on economic and financial conditions.
* More experienced RAs participate in econometric or theoretical research, write for Bank publications, and deliver speeches to civic and educational groups.
Required Education and Skills:
* Bachelor’s or master’s degree in economics or a closely related field, such as statistics, mathematics, or computer science.
* Coursework or experience in economics required; coursework or experience in econometrics, mathematics, statistics, and computer science highly desirable.
* Proficiency in programming languages and statistical software packages, such as Stata, R, Python, or Matlab, highly desirable.
* Strong academic record and experience with empirical research and data analysis highly desirable.
To Apply:
* Please attach a resume, cover letter, and unofficial transcript copy.
Incomplete applications will not be considered.
* Generally, non-U.S.
citizens are eligible to apply if they are able to obtain the legal status to work in the U.S.
for at least two years without sponsorship from the Bank.
F-1 visa holders with STEM OPT extension are eligible to apply.
* Please apply before November 30, 2025 to be considered.
We will review applications on a rolling basis, so applying early is recommended.
* Applications will be pre-screened prior to interview selections.
You will receive notification if you have been selected for a phone interview.
For more information on the Economic Research Department and the Federal Reserve Bank of Kansas City, ...
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Type: Permanent Location: Kansas City, US-MO
Salary / Rate: Not Specified
Posted: 2025-08-28 09:04:59
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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: 2025-08-28 08:52:40
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Papiertechnologe/-in (m/w/d) - Schicht
Job Description
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.
Deine Aufgaben:
* Unterstützung bei der sicheren und effizienten Bedienung der Papiermaschine
* Einhaltung von Sicherheits-, Umwelt- und Qualitätsvorgaben
* Mithilfe bei Farb-, Sorten-, Bespannungs-, Schaber- und Rollenwechseln
* Durchführung einfacher Qualitätskontrollen und Dokumentation
* Sicherstellung der Materialverfügbarkeit
* Verantwortung für Ordnung und Sauberkeit im Arbeitsbereich
* Zusammenarbeit im Team und Ausführung weiterer Aufgaben nach Anweisung
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:
* abgeschlossene Ausbildung zum/r Papiertechnologen/-in
* bereit, Schicht zu arbeiten
* gute MS Office-Kenntnisse
* Staplerschein und/oder Kranschein wünschenswert
* sehr gute Deutschkenntnisse
Was wir Dir bieten
Wir wollen mit Dir gemeinsam wachsen – daher bieten wir zahlreiche attraktive Weiterbildungsmöglichkeiten.
Du bekommst einen unbefristeten Vertrag.
Deine Vergütung richtet sich nach dem Tarifvertrag und wir legen noch...
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Type: Permanent Location: Koblenz, DE-RP
Salary / Rate: Not Specified
Posted: 2025-08-28 08:49:08
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We are currently seeking School Psychologists in the following areas:
Goshen, NY; Wappinger, NY; Sugar Loaf, NY; Ulster County
Liberty POST is currently seeking a motivated and energetic School Psychologist for per diem employment to work with children who are birth-5 years old through Early Intervention and Preschool Special Education programs.
Immediate positions are available.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994.
Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Evaluate, monitor and track child’s progress and adjust treatment plans accordingly.
* Test and evaluate child’s abilities to determine realistic goals.
* Record information on the initial evaluation, treatment, and progress in a timely manner using Electronic Medical Record system.
* Proficient at writing detailed analysis and reports.
* Effectively organize and maintain confidentially of child’s records and other documentations.
* Follow all state laws and regulations as it pertains to Early Intervention, CPSE/CSE special education.
Qualifications, Knowledge and Experience:
* Master's degree in School Psychology required
* Minimum of two years working with children in special education required
* Certification in NYS as a School Psychologist required
* Knowledge and experience administering standardized testing in the following areas: cognitive, achievement, behavioral/social-emotional and adaptive skills.
* Experience using Frontline (formerly IEP Direct) to assist in developing IEPs.
Benefits for this position:
* Health Benefits and Retirement packages available for FT positions
* Accrual of sick time based on NYS Sick time Laws
* Mentoring is offered to all providers
* Access to unlimited CEU courses offered that are accredited through ASHA, AOTA, APTA and CTLE
* Flexible scheduling
* Work with a team of professionals that care about making a difference
* Payment is biweekly with direct deposit
Job Type: Per Diem
Pay Rate:
* Evaluations - Psychological: $180
* Social History: $125
* Observation: $40
* CPSE meetings: $25
Liberty POST is an equal opportunity employer.
We offer equal employment opportunities to all persons without regard to race, color, ethnicity, religion, sex, sexual orientation, national origin,...
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Type: Permanent Location: Goshen, US-NY
Salary / Rate: Not Specified
Posted: 2025-08-28 08:40:45
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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
Job facts
As part of Roche Diagnostics CPS Near Patient Care (NPC), our department is involved in a multitude of projects ranging from blood glucose measurements to the development of cardiac and coagulation assays.
The NPC Analytics Subchapter is located in Mannheim supports various products from early R&D to launched products.
The main focus of the group is the development and validation of tailor made methods utilizing techniques of rheology, analytical particle characterization (PCS, SEM, Laser Scanning microscopy), surface analysis of membranes, fleeces, metals, plastics and coatings (XRF, NIR/IR, RAMAN), as well as troubleshooting topics.
Your main tasks
* Develop methods based on new and existing technologies to evaluate raw materials, production intermediates and final products of the NPC portfolio
* Documentation of testing procedures
* Continuous analysis and evaluation of materials and products at all stages of development
* Support for customer related investigations
Who you are
In hiring new employees, we look for people who are also inspired by our mission and who would fit in well with the collaborative spirit of the company culture.
Because we know that employees are critical to our success in bringing novel diagnostic solutions to patients, we are dedicated to remaining a great place to work and to providing employees with programs, services and benefits that allow them to bring the best to the business and to their personal lives.
To be successful in this role, you will be or you will have:
* Highly qualified and motivated Master student with a background in Materials Science, Polymer Science, Biomedical Engineering, Chemistry or related fields
* High motivation to work hands-on
* Experiences in Surface analytical methods (SEM, Stylus profilometry), Spectroscopy (UV/VIS, RAMAN, NIR, IR, XRF) and Microscopy (SEM, Laser scanning, fluorescence).
Additional knowledge in surface tension, viscosity and rheology would be beneficial
* As an intern within R&D Near Patient Care Analytics you could be expected to support both project and functional teams depending on the needs of the department
Your advantages
* Flexible time management
* 2092€ salary per month for a full-time internship > 3 months
* Reduced meal prices (-50 %) in our employee canteen
* Fitness center on the Roche campus
* Networking with other students
Your application
Please upload your Curriculum vitae specific to this po...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-08-28 08:38:48
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Nanjing, Jiangsu, China, Suzhou, Jiangsu, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% i...
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-08-28 08:36:54
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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:
Non-Standard
Job Sub Function:
Workday Associate D
Job Category:
Non-Standard
All Job Posting Locations:
Shanghai, China
Job Description:
* Support Site Record Coordinator to maintain the process of Document Control & Record Control under Ethicon Minhang Quality Management System.
支持工厂记录协调员进行爱惜康闵行质量管理系统下的文档控制和记录控制流程的维护。
* Support Site Record Manager for the execution of Record Management Program to ensure Record Management requirements and local procedures aligned to Franchise Record Management Policy and WWRIM Policy & associated standards.
协助工厂记录经理执行记录管理项目以确保记录管理要求和本地程序与事业部记录管理政策、WWRIM政策和相关标准保持一致。
* Maintain site document control and record control procedures to align with Franchise procedures, J&J Policy and regulation requirement.
维护工厂文档控制和记录控制程序以和事业部程序，强生政策和法规的要求保持一致。
* Update site internal document master list in a timely manner.及时更新工厂内部文档主清单
* Deliver the training of document Control & record control across whole plant.
对整个工厂进行文档控制和记录控制的培训
* Lead department record coordinators to implement site Record Management Program by executing the process of the archiving of Paper & Electronic records, control of Vital & Non-vital records, onsite record storage & offsite record storage.
组织部门记录协调员进行纸质和电子记录的归档、重要和非重要记录的控制、厂内和厂外记录保存流程以执行工厂记录管理项目。
* Take of Role of Quality Review Staff by following Product Release process for batch history record transfer and review activities.
依据产品放行程序负责质量审核人员的角色，以完成批生产历史记录的交接和审阅活动。
* Act as the backup of site training responsible and the site ComplianceWire Admin.
担任工厂培训人员的后援支持以及工厂ComplianceWire管理员。
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-08-28 08:35:56
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Chez PG Solutions, notre équipe de Croissance et Innovation relevant de la R&D regroupe plusieurs chefs de produits passionnés qui travaillent à transformer les solutions numériques destinées au secteur public.
Nous sommes actuellement à la recherche d’un Gestionnaire de produit (Product Owner) pour piloter l’évolution de notre gamme de produits en évaluation foncière et géomatique, dans un contexte de refonte vers une plateforme web moderne.
Le Gestionnaire de produit joue un rôle central dans notre démarche d’innovation.
Il agit comme lien stratégique entre les clients, la direction, l’équipe des ventes et l’équipe de développement, afin de faire évoluer le produit en réponse aux besoins du marché, aux tendances technologiques et aux exigences réglementaires.
Joueur clé au sein d’une équipe multidisciplinaire, la personne recherchée doit faire preuve de rigueur, d’autonomie et d’un excellent sens de la collaboration.
Elle est responsable de maintenir une vision claire du produit, de bâtir un plan d’évolution cohérent, et de mobiliser les parties prenantes autour de cette vision.
En collaboration avec l’équipe de développement, elle analyse les besoins des clients, propose des solutions concrètes, identifie les fonctionnalités clés et les communique de façon claire et structurée.
Profil recherché:
Nous sommes à la recherche d’une personne rigoureuse, curieuse et dotée d’un fort esprit de collaboration, possédant une bonne connaissance du domaine de l’évaluation foncière municipale au Québec, notamment en ce qui concerne le cadre réglementaire et les pratiques professionnelles en vigueur.
Une bonne compréhension des concepts et des outils en géomatique, tels que les systèmes d’information géographique (SIG), les données spatiales et la cartographie, constitue également un atout important.
Votre rôle:
* Actuellement, nous modernisons notre solution d’évaluation foncière en la faisant évoluer vers une plateforme web innovante, performante et conforme aux normes professionnelles du Québec.
Notre produit intègre également un important volet géomatique, essentiel à notre approche.
* En tant que Gestionnaire de produit, vous serez au cœur de la refonte de notre produit.
Vous piloterez la vision, la stratégie et l’évolution fonctionnelle de la solution, en collaboration avec les parties prenantes internes et externes.
Vous contribuerez à bâtir une plateforme web moderne, intuitive et conforme aux exigences réglementaires et aux meilleures pratiques du domaine.
Responsabilités:
* Compréhension du domaine et des utilisateurs
* Apprendre les systèmes, les processus de travail et les réalités opérationnelles de nos clients.
* Recueillir, analyser et documenter les besoins des utilisateurs, en clarifiant la portée des demandes.
* Représenter les utilisateurs et les parties prenantes auprès de l’équipe de développem...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 85000
Posted: 2025-08-27 09:43:38
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Join a community where people come first.
Systems & Software, a division of Harris, is hiring a Support Analyst to join our collaborative, community-driven team.
At Harris, you are not just a number: you are part of a culture that values continuous learning, mutual support, and personal growth.
As a Support Analyst, you will play a key role in delivering exceptional customer service.
You will engage directly with clients to resolve technical issues, manage support tickets, and identify when to escalate code-related challenges to our development team.
Your ability to communicate clearly, manage your time independently, and build trusted relationships will make you a valued part of our client success story.
This is more than just a support role.
It is an opportunity to grow within a community that invests in you, values your contributions, and fosters a strong sense of community across all levels.
Occasional travel may be required, offering even more opportunities to connect and learn.
If you are passionate about helping others, thrive in a people-first environment, and want to be part of a team that truly supports one another, we invite you to apply.
This role is looking for candidates based in Atlanta, Georgia, with required travel one week per month.
Each month requires one week of on-site work in the DeKalb utility area, one week in Atlanta, and the remainder of the month remote from home.
Additional travel may include annual group meetings in Vermont.
What your impact will be:
* Handle support calls or tickets.
* Install and update product line applications, integrated third party applications, and operating system and database applications.
* Exercise sound professional judgment in investigating technical problems.
* Collect detailed information to categorize requests and establish a method of resolution.
* Document all customer communication through tickets.
What we are looking for:
* Minimum one year of customer service experience in a technical environment or relevant experience.
* Proven problem-solving abilities.
* Strong verbal skills and exceptional written communication.
* Experience in technical documentation.
* Ability to multi-task effectively.
* Ability to work independently with minimal supervision.
* Provide onsite attention and support for specific clients.
Travel and onsite visits are required.
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 govern...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: 70000
Posted: 2025-08-27 09:43:35
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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: Quality Assurance Intern
As a Quality Intern, you will be part of the Fort Dodge Quality Assurance team to support activities related to the oversight of manufacturing and distribution of commercial products.
There will be several opportunities to gain experience in different areas within Quality, such as Quality Management System, Pharmaceutical Products, and Audits.
Your Responsibilities:
* Defining, measuring, analyzing, and improving identified processes within the quality organization.
* Understand the Manufacturing processes and how Quality supports the process and business.
* Work within cross-functional teams to support inspection readiness activities, investigations, and continuous improvement projects.
* Get real-world experience in the regulated environment.
* Assist with the production and analytical processes the ensure they are carried out with appropriate Sterility Assurance standards.
* Study design improvement process.
What You Need to Succeed (minimum qualifications):
* Education: Currently enrolled in an undergraduate program with a concentration in Science (Biology, Chemistry, Biotechnology, or related field) or Engineering.
* Effective communication and interpersonal skills.
* Strong organizational and time management skills
* A willingness to learn.
* Must be able to work exceptionally well independently and with minimal supervision.
What will give you a competitive edge (preferred qualifications):
* Have an interest in animal health manufacturing, problem solving, scientific method, or cross-functional skill development.
* Thrive in cross-functional team settings.
Additional Information:
* Travel: 0%
* Location: Fort Dodge Manufacturing Plant - Fort Dodge, Iowa
Our Internship Program
Our internship program is designed to provide students with experiences! Internships are project based and comprised of business-critical needs.
All interns have the opportunity to significantly impact Elanco’s success over the summer and kickstart a career t...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2025-08-27 09:42:44
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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: Senior/Principal Scientist, Downstream Process Development
The Biopharma Technical Development team located in Indianapolis, IN is seeking a Senior/Principal Research Scientist to provide scientific and technical expertise for the development and launch of new biological drug substances in an innovative and fast-paced organization.
This role is focused on downstream process development with an emphasis on monoclonal antibodies, therapeutic proteins, and other biological modalities.
You will be responsible for leading downstream process development activities at bench and pilot scales, supporting scale-up, technical transfers, process implementation, and clinical material production at both internal and external manufacturing sites.
In addition to technical excellence, this position requires strong organizational management, communication skills, and cross-functional collaboration across departments and geographies.
As a subject matter expert in downstream process development, you will have the potential to lead both projects and people.
Your Responsibilities:
* Provide scientific expertise in downstream process development for early- and late-stage biologic programs (mAbs, therapeutic proteins, and other modalities) using phase-appropriate development strategies.
* Apply Quality by Design (QbD) principles to process development and process characterization.
* Lead and contribute to risk assessments supporting product development stage-gate reviews and robust manufacturing control strategies.
* Develop representative scale-down models from commercial-scale operations and apply prior knowledge to guide development studies.
* Author and review source documents for regulatory submissions; respond to CMC questions from regulatory agencies.
* Partner with R&D, Technical Services/Manufacturing Sciences (TS/MS), supply chain, Quality, Manufacturing, Launch Leaders, external CDMOs, and other stakeholders to ensure successful tech transfers and commercialization.
* Serve as a technical resource to Biopharma Technica...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-08-27 09:42:43
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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: Global Quality Auditor
As a Global Quality Auditor, you will be part of the Elanco Global Quality Compliance and Auditing (EGQCA) organization.
In this role, you’ll be responsible for assuring compliance with company standards and regulatory requirements through internal and external audits of pharmaceutical products and commercial operations.
Your Responsibilities:
* Schedule, prepare, conduct, and report Global Quality audits and assessments of commercial operations.
* Participate in or lead the risk assessment of commercial operations and influence actions within EGQCA and business areas.
* Drive the escalation of compliance issues or significant risks identified during audits or risk assessments.
* Maintain strong interpersonal and communication skills, with an emphasis on verbal and technical writing.
* Lead in the assessment of Top 10 product supply chain audits and conduct Due Diligence audits for new acquisitions.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree (or equivalent work experience) in physical or biological sciences, Engineering, or other technical area.
* Required Experience: A minimum of 5 years of previous auditing experience in aseptic manufacturing platforms.
* Ability to analyze detailed technical scientific information and interpret/apply regulations; excellent interpersonal and communication skills.
What will give you a competitive edge (preferred qualifications):
* Ability to work under pressure on multiple tasks concurrently and meet deadlines.
* Proven ability to think and analyze from a process perspective; project management skills.
* Ability to process information to identify linkages and trends for compliance strategies.
* Ability to work independently and collaboratively within a global team environment.
* Ability to influence and manage change/conflict, and be pragmatic in decision making.
Additional Information:
* Travel: Up to 50% (domestic and international, trip duration 1-2 weeks), somet...
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Type: Permanent Location: Warszawa, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-08-27 09:42:38
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Financial Planning & Analysis Lead
Job Description
Financial Planning & Analysis Lead
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.
In this role, you will:
Responsibilities
Budgeting & Forecasting
* Lead and coordinate with cross functionals team to come up with budgets, forecasts backed by set of strong key assumptions, help ensure consistency with sound business management and corporative objectives.
* Ensure timely & quality of financial forecast & budget submission to Regional & Segment team.
* Support CFO in preparation of forecast presentation.
* Work as Vietnam Finance representative in developing new financial forecasting tools as well as in other Global initiatives.
* Work with Managing Director and HoDs for a long-term strategic plan and co-ordinate to drive initiatives to deliver that plan.
Performance Management
* Lead monthly business review process with Local and Regional stakeholders.
Track monthly progress against targets, providing timely visibility of gaps, potential deviations versus quarterly and full year projections and insightful analysis in key metrics
* Lead performance discussion to identify gap closing plan.
Work with cross functions to deliver that plan
* Lead actual management reporting & result submission to Regional & Segment team
* Prepare presentation material for Monthly Business Review and other presentations per requirements of CFO
* - Prepare landing estimate and discuss the landing view with CFO on monthly basis
* Support scenario planning and financial analyses on a case-by-case basis as per requirements of CFO
Process Improvement – Simplification, Standardization & Automation
* Identify and make recommendations that optimise business processes and improve financial and other internal controls
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 more than 150 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 per...
....Read more...
Type: Permanent Location: District 4, VN-SG
Salary / Rate: Not Specified
Posted: 2025-08-27 08:56:03
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Enterprise Supply Chain FP&A Analyst
Job Description
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.
This global role will serve as the key financial point of contact for Kimberly-Clark's FP&A initiatives with a focus on the Wave program, overhead cost center budgeting and managing and tracking global incentives.
The ideal candidate will possess strong analytical skills, a keen attention to detail, and the ability to engage effectively with various teams and stakeholders across the globe.
Additionally, the candidate will be a strategic thinker, identifying opportunities and driving value for the ESC team on a global scale.
In this role, you will:
* Act as the primary financial liaison for the Wave program, ensuring accurate financial reporting and analysis on a global level.
* Lead the overhead cost center budgeting process for ESC, including planning, forecasting, and variance analysis.
* Manage and track global incentives, ensuring compliance with corporate policies and procedures across different regions.
* Collaborate with cross-functional teams worldwide to provide financial insights and support decision-making processes.
* Identify and implement process improvements to enhance financial reporting and analysis on a global scale.
* Prepare and present financial reports and presentations for senior management, highlighting global financial performance and strategic opportunities.
* Conduct comprehensive ad-hoc financial analysis and reporting as needed to support global initiatives.
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 more than 150 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 make...
....Read more...
Type: Permanent Location: Roswell, US-GA
Salary / Rate: Not Specified
Posted: 2025-08-27 08:56:01
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Community Health Project Los Angeles (CHPLA) is a program of Heluna Health.
CHPLA’s mission is to improve the health and wellbeing of people affected by substance use in Los Angeles, to increase access to health care, empower people to protect themselves, and educate each other to reduce harm in our communities.
CHPLA combines direct services, advocacy, outreach, education, and research collaborations to fulfill this mission.
Community Health Project Los Angeles was founded in 1992.
Law Enforcement Assisted Diversion (LEAD) is a community-based diversion approach with the goals of improving public safety, and reducing unnecessary justice system involvement of people who participate in the program.
In a LEAD program, law enforcement officers exercise discretionary authority at point of contact to divert individuals to a community-based, harm-reduction intervention for law violations driven by unmet behavioral health needs.
In lieu of the traditional criminal justice system cycle -- booking, detention, prosecution, conviction, incarceration -- individuals are instead referred into a trauma-informed, harm reduction intensive case-management program where the individual receives a wide range of support services.
Prosecutors and law enforcement work closely with case managers to ensure that all contacts with LEAD participants going forward, including new criminal prosecutions for other offenses, are coordinated with the service plan for the participant to maximize the opportunity to achieve behavioral change.
There are certain core principles to LEAD that are essential to achieve transformative outcomes.
These include LEAD’s harm reduction/Housing First framework, which requires a focus on individual and community wellness, rather than an exclusive focus on sobriety; and police officers and sergeants involvement as meaningful and positive meaningful partners in program design and operations.
The LEAD Case Manager reports to the CHPLA’s Program Manager and Clinical Supervisor.
The Case Manager position will provide field based intensive case management services to participants of CHPLA harm reduction programming.
The Case Manager will provide direct services to assigned participants (approximately 20 case load), and coordinate care by meeting with participants regularly, assessing needs and facilitating access to appropriate resources.
The Case Manager must develop and maintain positive collaborative relationships with community partners, and other service providers in order to best serve their participants.
This is a full time, benefitted position (40 hours per week).
Employment is provided by Heluna Health.
If hired for this position, you will be required to provide proof that you are fully vaccinated for COVID-19 prior to your start date, or have a valid religious or medical reason qualifying you for an exemption (that may or may not require accommodation).
The pay rate for this position is $29.25 per hour.
ESSENTIA...
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Type: Permanent Location: los angeles, US-CA
Salary / Rate: 29.25
Posted: 2025-08-27 08:47:03
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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:
Non-Standard
Job Sub Function:
Non-Employee
Job Category:
Non-Standard
All Job Posting Locations:
Beijing, China, Shanghai, China
Job Description:
The Epidemiology APAC team is a division of Global Epidemiology Orginization, Johnson & Johnson.
The Epidemiology APAC team exists to be experts in generating, leveraging, and promoting the use of high-quality Real-World Evidence for various stakeholders.
The team shows up every day determined to maximize the utility of Real-World Evidence to achieve regulatory and business priorities.
The team is recruiting an Epidemiology Senior Scientist / Manager in Shanghai/Beijing, China depending on the candidate’s expertise and experience.
The Epidemiology Senior Scientist / Manager will work under the supervision of senior members of the Epidemiology APAC team, the research leader in academia in multiple therapeutic areas in China.
The role will involve participation in various task forces in addressing issues raised by the clinical teams/regulatory agencies by providing epidemiology and statistical support.
The role will be expected to keep up to date with the China real-world data, and communicate with the cross functions or stakeholders in support of the team’s projects.
The primary responsibilities will be:
- to deliver individual programming deliverables (tables, listings, figures and other reports) of projects with low to medium complexity.
- to develop quality control checks for programs or output.
- to develop the statistical analysis plan and maintain programming documentation as appropriate.
- to establish, maintain access, and collaboration with real-world data holders or researchers in China.
- to participate in the development and review of study-specific procedures
- to communicate with internal and external stakeholders to ensure the final high-quality deliverables
Qualifications:
* At least a bachelor’s or master’s degree in Epidemiology, Biostatistics, or Public Health is required.
A minimum of 3 years of experience in the related field is also required.
* Proficiency in SAS programming or other statistical software (such as R, Python) is required.
* Programming and analyzing experience in large real-world databases are highly preferred.
* Ability to work on multiple projects simultaneously is also preferred.
* verbal and written communication skills in China and English (Reading, writing, and sp...
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-08-27 08:30:32
