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Are you ready to dive into the dynamic world of Support Analysis? Here at Cayenta; a division of Harris, support calls are an exciting puzzle, typically falling into one of three thrilling categories: Application issues, Environment and Database issues, and IT/Communications issues.
As a Support Analyst, your focus will be on the intriguing realm of software application issues.
This is your chance to deepen your expertise in the solutions used by our CIS customers.
Whether you're in Canada or the United States, we're looking for talented individuals like you to join us remotely.
Embrace the challenge and become a pivotal part of our support team from wherever you are!
This remote role welcomes candidates anywhere in Canada and the US.
What your impact will be:
* Provide timely and thorough resolution to customer issues.
* Monitor the support call queue and take ownership or re-assign new tickets.
* Interact with a range of internal departments (Environment Specialist, R&D, other analysts, etc.) for issue escalation.
* Assist in the problem solving of data, architecture, and interface issues.
* Respond quickly to customer calls and provide frequent updates so customers know their problems are being addressed.
* Develop a deep understanding of the functional and technical features of our applications and use this knowledge to address application-related issues and questions.
* Provide recommendations to customers and Product Management to prevent recurrence of the issue.
* Understand the support services agreement to know when requested services are outside the support agreement terms.
* Provide suggestions on enhancements to the product or process.
What we are looking for:
* A University degree or technical college degree in computer sciences, software engineering, software development or related field is preferred.
* Experience delivering solutions, services and/or support to the utility industry is preferred.
* Experience with Customer Information Systems preferred.
Customer Support Qualifications
* Familiarity and experience in a Customer Support environment.
* Excellent client communication skills. Ability to manage and shape customer expectations.
* Ability to work on multiple initiatives and/or support tickets simultaneously.
* Strong analytical problem-solving skills.
Must be able to analyze information to make independent decisions quickly and effectively.
* Ability to work independently, be flexible, be self-motivated and be a team player.
* Utility industry experience is preferred.
Technical Qualifications
* Software experience in applications based in at least one of the following is preferred: Java, SQL, PL/SQL, Uniface, Web technologies (Node.js, Angular, JavaScript, JSP).
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your f...
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Type: Permanent Location: Victoria, CA-BC
Salary / Rate: 65000
Posted: 2025-05-15 08:53:53
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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 Control Associate, Immunochemistry
The Quality Assistant performs bio-analytical testing (primarily ELISA) on various sample types (raw materials, in-process, release, stability) following regulatory guidelines (9CFR, EU, VICH) and company SOPs.
This role involves initiating, executing, and completing assays while ensuring timely communication with supervisors regarding testing progress, compliance, or scheduling challenges.
Additionally, the Quality Assistant maintains a safe work environment and adheres to GMP documentation practices, with further duties assigned based on experience level.
Your Responsibilities:
* Performs ELISA and PCR testing on in-process, release, and stability samples.
* Prepares reagents and maintains calibrated equipment essential for testing.
* Analyzes test results and reports data using designated software systems.
* Manages inventory, orders necessary kits/supplies, and monitors critical reagent consumption.
* Reviews, updates standard methods, and collaborates with relevant personnel (QC Media Kitchen, Senior Scientists, Supervisors, Managers, Directors) for support and problem-solving.
What You Need to Succeed (minimum qualifications):
* Bachelor’s degree in scientific discipline (e.g., Biology, Biochemistry, Microbiology, etc.) (preferred), Associate degree with laboratory experience, or equivalent laboratory experience in lieu of degree
* Strong understanding of scientific principles, basic lab techniques and immunochemistry processes.
* Ability to performs and document work following established methods, SOP's, GLP/GCP and/or cGMP.
What Will Give You the Competitive Edge (preferred qualifications):
* Problem solving within the scope of responsibilities with some guidance from Supervisor.
* Strong ability to document lab results / data in a lab notebook following applicable regulations.
Additional Information:
* Laboratory work: 80% Lab work, Documentation 20%
* Location: Fort Dodge, Iowa
Don’t meet every single requirement? Studies ...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 31.93
Posted: 2025-05-15 08:53:19
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Job Description
Job Description
The Materials Design Lab, led by Professor Jae Chul Kim in the Department of Chemical Engineering and Materials Science (CEMS), invites applications for a Postdoctoral Researcher position in the field of electrochemical energy storage systems.
The successful candidate will conduct original and innovative research focusing on:
* Design of novel cathode materials and interfaces for next-generation lithium-ion batteries.
* Atomic-resolution structural characterization using advanced electron microscopy techniques.
This full-time position is available starting May 19, 2025, or later, and is suited for a highly motivated researcher aiming to thrive in a dynamic and fast-paced research environment.
Duties and Responsibilities
* Perform research and development of advanced materials for energy storage applications.
* Lead experiments in battery fabrication and electrochemical testing.
* Conduct atomic-scale analysis of materials using electron microscopy and, when applicable, synchrotron-based techniques.
* Analyze electrochemical, spectroscopic, and scattering data from in-house and national lab beamline facilities.
* Collaborate closely with graduate students and other research staff.
* Present findings at conferences and contribute to scholarly publications.
* Assist with grant writing and proposal development when necessary.
Required Qualifications
* Ph.D.
in Materials Science and Engineering, Chemical Engineering, or related field by the time of appointment.
* Background in energy storage materials.
* Demonstrated hands-on experience in battery fabrication and electrochemical testing methods.
Department
Materials Science and Engineering
General Submission Guidelines:
Please submit an online application to be considered a candidate for any job at Stevens.
Please attach a cover letter and resume with each application.
Other requirements for consideration may depend on the job.
Still Have Questions?
If you have any questions regarding your application, please contact Jobs@Stevens.edu.
EEO Statement:
Stevens Institute of Technology is an Equal Opportunity Employer.
Accordingly, Stevens adheres to an employment policy that prohibits discriminatory practices or harassment against candidates or employees based on legally impermissible factor(s) including, but not necessarily limited to, race, color, religion, creed, sex, national origin, nationality, citizenship status, age, ancestry, marital or domestic partnership or civil union status, familial status, affectional or sexual orientation, gender identity or expression, atypical cellular or blood trait, genetic information, pregnancy or pregnancy-related medical conditions, disability, or any protected military or veteran status.
Stevens is building a diverse faculty, staff, and student body and strongly encourages applications from people of all backgrounds.
Stevens is a federal contracto...
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Type: Permanent Location: Hoboken, US-NJ
Salary / Rate: 65000
Posted: 2025-05-15 08:27:05
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Main Responsibilities
* Prepare lab samples and customer trail batches to compare the quality of the samples.
* Manipulate new or existing formulations to obtain required properties through adjustment of raw materials or processing parameters that meet customer expectations and are commercially successful.
* Maintain concise and accurate record keeping ensuring compliance with internal and external standards.
* Provide technical assistance to internal departments and customers.
* Communicate effectively with suppliers, internal customers, and external customers.
* Conduct performance and quality tests throughout the process as required.
* Ensure and maintain a safe and orderly working environment for all employees.
* Assist with manufacturing scale up of batches and formulations.
Key Qualifications
* Bachelor’s Degree in Chemistry or closely related field, or 6+ years of solvent based laboratory experience in lieu of a degree.
* 3+ years of formulation experience including direct experience with solvent borne coatings systems (alkyd, amino chemistries with acid cure).
Preferred Qualifications
* Ability to draw conclusions and make recommendations based on experiments.
* Strong written and verbal communication skills.
* High degree of proficiency with multiple computer systems (Office 365, Product Vision, D365, Salesforce).
* Able to work in a team environment, complying with required housekeeping and safety expectations.
* Detail oriented and the ability to comply with internal reporting requirements (notebooks, formulation sheets).
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Type: Permanent Location: Greensboro, US-NC
Salary / Rate: 72500
Posted: 2025-05-15 08:20:32
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
This position is fully remote and you must live in the West Virginia area
Purpose:
Established and productive individual contributor, who works under moderate supervision.
Helps implement projects, programs, and processes in support of the organization's overall Clinical Sales - Hospital/Hospital Systems strategy.
Applies practical knowledge of the Clinical Sales - Hospital/Hospital Systems field to administer best in class policies, procedures, and plans for the area.
Territory Managers are responsible for cold calling, prospecting, and building relationships that will increase account revenue growth and customer satisfaction within specified product lines and geography.
Focus areas will include driving new business with responsibility for achieving sales expectations in an assigned territory while providing exceptional service and support to physicians to meet their patient’s needs.
The Territory Manager is responsible for case coverage in catheter labs while w...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-15 08:16:38
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ERM is seeking an experienced Principal Technical Consultant, Ecologist (Scientist or Biologist) with consulting experience to play a key role in implementing our existing programs in our Ewing, New Jersey office.
The ideal candidate will have served as a senior subject matter expert in the ecological field with a proven track record of high-quality outputs, experience working within a variety of ecological media and settings, and excellent client communication skills and responsiveness.
This is a fast-track opportunity for a senior-level professional looking to advance their career with a global environmental leader, on existing contracts.
Business Development will not be required at the onset of this role.
The role will be predominantly desktop with some site visits.
RESPONSIBILITIES:
* Coordinate environmental investigations of surface water, sediments, and wetlands by preparing or reviewing sampling plans in accordance with applicable New Jersey Department of Environmental Protection (NJDEP) regulations and guidance.
* Contribute to preparing technical documents such as Ecological Evaluations and Ecological Remedial Investigation Reports by leading project teams through the data evaluation of soil, groundwater, surface water and sediment sampling results.
* Oversee riparian and wetland restoration projects in New Jersey under the auspices of the NJDEP and Natural Resource Trustees.
* Support ecological risk assessments by coordinating with the data team to process and interpret data for use by the risk assessor.
* Support land use and wetlands permitting efforts pursuant to NJDEP programs.
* Achieve client’s expectations for scope, budget, schedule, and quality.
* Maintain positive relationships with clients and public agencies.
* Other duties may include natural resource surveys, biological monitoring (as necessary), field team management, and providing specialized site assessments.
REQUIREMENTS:
* BS or MS in biology, wetland science, plant ecology or similar field with experience pertaining to a specialized biological training or field.
Or equivalent experience.
* 6+ years (8+ years preferred) of consulting experience that involves oversight, QA/QC, technical writing, ecological evaluations, and multi-media permitting.
* Solid grasp of the key biological or wetland ecology impact assessment and management issues within various industry sectors, as well as a high degree of technical competence and broad knowledge of impact assessment best practices.
* Knowledge of state and federal environmental regulations.
Experience with NJDEP’s Bureau of Environmental Radiation (BER) is a plus.
* Recognized technical expertise by and established reputation in the marketplace, including positive reputation with key regulators relevant to ecological assessment approvals.
* Well-developed team building and influencing skills; unquestioned integrity; and ...
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Type: Permanent Location: Ewing, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-15 08:15:16
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Company
Federal Reserve Bank of Cleveland
The Federal Reserve Bank of Cleveland is part of the nation’s central bank and we’ve provided many opportunities for professional growth during our history.
For twenty-five years in a row, we’ve been named “One of Northeast Ohio’s Best Places to Work” by North Coast 99.
This prestigious award honors organizations with outstanding employment practices, including compensation, benefits, training, recruitment, retention, community services, and employee communications.
Our People Make the Difference! The Federal Reserve Bank of Cleveland is seeking innovative thinkers with vision to build the framework that will carry the Bank into the future.
Follow us on LinkedIn, X, Instagram, and our YouTube channel – Cleveland Fed
Job Description:
The PHD Fellows will conduct research that contributes to the Center for Inflation Research and other Bank Research initiatives leveraging their expertise with time series econometrics, asset pricing, and business cycle theory.
In addition to their research projects, the PhD Fellows will collaborate with department economists and attend research seminars to develop their research expertise.
Number of hours worked per week: 40 hours per week
Beginning and ending dates: TBD (June through August)
Physical Demands and General Working Conditions
This is not necessarily an exhaustive list of all responsibilities, duties, performance standards or requirements, efforts, skills or working conditions associated with the job.
While this is intended to be an accurate reflection of the current job, the Federal Reserve Bank of Cleveland reserves the right to revise this or any job description at any time.
Reasonable Accommodation Statement - The Federal Reserve Bank of Cleveland is committed to ensuring that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment.
To request a reasonable accommodation for any part of the employment process, please send an email to clev.4d.benefits.specialist@clev.frb.org.
Bank’s Ethics Rules and Drug Testing
As a condition of employment, Federal Reserve Bank of Cleveland employees must comply with the Bank’s ethics rules which generally prohibit employees, their spouses/domestic partners, and minor children from owning or controlling, directly or indirectly, any debt or equity interest in a depository institution or an affiliate of a depository institution.
A "depository institution" means a bank, a trust company, or any institution that accepts deposits, including a bank chartered under the laws of a foreign country.
In addition, employees (and their spouses/domestic partners, and minor children) may not own shares of mutual funds, unit investment trusts or ETFs that have a policy, as stated in the prospectus, of concentrating in the fi...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-14 12:57:33
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Position Description:
To increase penetration of swine products by guiding KA (Key Account), key farm, specialized dealer and KOL (Key Opinion Leader) through executing educational/promotional seminars, providing professional knowledge, service & product knowledge and sharing information
Functions, Duties, Tasks:
* Provide consultation on swine farming and health care to customers.
* Hold educational/promotional seminars and deliver professional knowledge for internal/external customers.
* Update technical information for swine and work with AHP in the field.
* Make projects such as full value experience and trial.
* Collect industry information, competitor’s activities and customer needs to be reflected on country species business strategy.
* Work closely with PM, RA and sales representatives to align with marketing & technical strategies for each product.
* Be a company representative for professional communities such as swine vet society, swine disease research institute and swine integrated companies.
* Report to FA Technical & Vaccine Marketing Lead
Minimum Qualification (education, experience and/or training, required certifications):
* Education: Doctor of Veterinary Medicine
* Experience: at least 3 years’ experience in animal health industry or animal production
* Should have good communication skills including presentation and managing interpersonal relationships.
* Should be results-oriented, positive, enthusiastic, self-motivated, challenging against changes and difficulties.
Additional Preferences:
* Good communication on products and business with external variety of customers.
* Providing quality technical services to customer to convince company and product quality
* Can extend and communicate with other species like poultry and cattle
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status...
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Type: Permanent Location: Seoul, KR-11
Salary / Rate: 63000000
Posted: 2025-05-14 12:38:53
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Voici l’occasion de vous joindre à l’équipe d’ACCEO Solutions, une division de Harris Computer, là où les employés sont au cœur de nos préoccupations! ACCEO Solutions vous offre un environnement de travail qui reflète concrètement nos valeurs telles que la qualité, la créativité, le respect, la responsabilité et l’intégrité.
Relevant de l’assistant contrôleur, l’agent de collection qui se joindra à notre équipe sera reconnu pour être débrouillard, curieux, motivé, proactif, avoir de l’entregent et faire preuve de minutie.
Ce qu’on attend de vous :
* Faire le suivi et la collection des comptes clients pour les unités ACCEO Estimation, Gestion CMEQ et Service de Garde;
* Préparer des dépôts et mettre à jour des comptes clients avec les paiements reçus;
* Répondre aux demandes d’information des clients et collaborer avec les collègues à l’interne;
* Aide à la facturation client pour l’unité ACCEO Estimation et Gestion CMEQ;
* Participer à la préparation de certaines analyses;
* Apporter votre support au reste de l’équipe des finances;
* Effectuer toutes autres tâches administratives demandées.
Ce qu’il vous faut :
* Formation post-secondaire en comptabilité, administration ou toute autre formation jugée équivalente;
* Bonne connaissance des logiciels Microsoft Office Excel & Outlook;
* Connaissance générale des logiciels comptables, modules clients;
* Une bonne maîtrise du français et de l’anglais est requise, car le titulaire du poste aura à communiquer fréquemment dans les deux langues, tant oralement que par écrit, car nous avons des collègues, des clients et des partenaires au Québec, ainsi que dans le reste du Canada et aux États-Unis.
Points bonis si :
* Expérience en comptabilité;
* Expérience en service à la clientèle;
* Expérience avec un logiciel ERP intégré, particulièrement Microsoft D365 (atout).
En plus d’une équipe incroyable, nous vous offrons :
* Télétravail 100% avec équipements fournies;
* 3 semaines de vacances + 5 jours de congé personnel par an;
* Assurances collectives payées par l’employeur, dès le premier jour;
* Programme Lifestyle Rewards, 325$ par an;
* Programme de REER Matching, programme d’actionnariat, de référencement et beaucoup plus;
*Seul les candidats retenus seront contactés
*
Harris souscrit à un programme d’accès à l’égalité en emploi et les candidatures des membres des groupes visés à savoir les femmes, les personnes handicapées, les personnes autochtones et les minorités visibles sont encouragées à soumettre leur candidature.
Si vous êtes une personne handicapée, vous pouvez recevoir, sur demande, de l’assistance pour le processus de présélection et de sélection.
L'équipe de recrutement de talents de Harris n'a pas recours aux messages texte pour entrer en communication avec les ...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-05-14 12:37:06
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MediSolution is seeking a Customer Support and Implementation Specialist with a solid background in Financial processing and reporting within the Healthcare industry.
As a Customer Support & Implementation Specialist, you will work closely with both clients and development team members to achieve client goals.
You will be the frontline point of contact providing high quality, friendly, and prompt technical support.
Responsibilities include overall project management, creation of project deliverables, implementation, client training, demonstration, program documentation, and product testing. The ideal candidate must be a team player with strong people skills, self-learning skills, and share a dedication to the latest technologies and techniques.
To excel in this role, you’ll need to have an analytical mind and a passion for digging into the details to find unique solutions to complex problems.
You’ll need to be able to leverage your natural curiosity to help you thrive in ambiguity and tackle problems.
What your impact will be:
* Provide high quality support to our clients, ensure we are meeting contractual obligations and maintaining a high level of customer satisfaction and timeliness of resolution;
* Communicate to clients when there are changes to the application, and occasionally regulatory and legislative updates;
* Implement new customers from start to finish including but not limited to analyzing set up needs, testing, training;
* Provide ongoing customer support including; troubleshooting issues, providing application training to new staff, including reporting training on an Excel-based application;
* Prepare and keep up to date training documentation and update user guides when needed;
* Assist with business development-related activities including the development of proposals, statements of work, and delivery of presentations;
* Participate in project planning and implementation;
* Develop a deep understanding of the functional / technical features of our applications and use this knowledge to address application-related issues and questions;
* Troubleshoot software and implementation issues and provide workaround and functional implementation guidance as needed, completing support cases for clients with a quick turnaround; via telephone, email, and/or ticketing system;
* Use ticketing system to review tickets, prioritize ticket queue, update and resolve tickets with complete and accurate documentation in a timely and effective manner;
* Diagnosing and documenting software issues / bugs, performing the appropriate resolution; working with other members of the technical support and software development teams in order to identify and resolve problems in a timely, efficient, and effective manner;
* Design of new product features alongside members of the software development team;
* Perform other duties as required or assigned.
What we are looking for:
...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-05-14 12:36:58
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Your Job
Are you passionate about exploring new ideas and breaking through conventional norms? At Georgia-Pacific, we share your enthusiasm for pushing boundaries and embracing creative solutions.
We constantly challenge the status quo, take calculated risks, and strive to improve the products we make.
Embark on the journey with us as a Product Developerto help us extend our competitive edge for GP PRO products.
As a product developer, you will have the unique opportunity to (1) deepen your technical expertise in product design, (2) leverage your creativity to tackle challenging problems, and (3) apply a customer-centric approach to driving innovation.
It's likely you regularly interact with the products we make, whether using a public restroom, dining out, or enjoying hotel amenities.
These products are designed to fit your needs and the needs of the establishment.
Our product developers think through these customer and end-user needs to design, manufacture, and deliver advantaged products.
There's more than meets the eye for these products with challenging technical problems to explore!
Our Team
The Georgia-Pacific PRO product development team drives the technical advancement of our tissue, towel, napkin, wipers, and skincare brands in the away-from-home market.
As a team of dedicated entrepreneurs, we're committed to ongoing innovation and cross-functional collaboration to solve complex problems and deliver meaningful value to our customers and the company.This position is located at the Neenah Technical Center (NTC), the central site for research, development, and lab services for Georgia-Pacific's North American Consumer Products business.
What You Will Do
Product Support:Provide technical support on product claims, data substantiation, intellectual property, and overall product points of view to our business teams and other capability partners.
Design and Experimentation:Designing and conducting experiments to test new product designs and hypotheses, analyzing data sets using advanced statistical methods and data analysis tools to support strategic decision-making.
Collaboration:Work with business stakeholders, consumer research, quality, operations, device development group, and our technology platforms to drive year-over-year cost & product improvements.
Career Development: Helping you grow and develop is important.
We'll help match your individual strengths and passion areas to high value projects, and you'll be able to leverage the internal network within GP and Koch Industries to share your technical expertise and learn from others.
Who You Are (Basic Qualifications)
* Bachelor's degree in physical science, paper science, or engineering
* Experience working in an R&D, product development OR manufacturing environment independently leading technical projects
* Able to travel an average of 25%.
What Will Put You Ahead
* Experience in paper manufacturing or paper products R&D
* Advanced degreein physic...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-05-14 12:20:10
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
Johnson & Johnson MedTech – Neurovascular division is currently seeking a Marketing Manager, GSM. This is a hybrid role based in Irvine, California.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech/
Key Responsibilities:
· Identify appropriate sources of market intelligence and apply analytics to make clear, data-based decisions
· Interface with physicians and broad international customer base to identify market trends and unmet clinical needs for the treatment of neurovascular disease
· Translate customer needs into product design requirements to develop differentiated product concepts
· Closely collaborate with R&D to provide customer insights during the product development cycle
· Build collaboration with cross-functional partners including regulatory, clinical affairs, professional and commercial education, supply chain and sales team to ensure seamless product commercial readiness
· Collaborate with global marketing partners to communicate product portfolio updates, understand local customer needs and coordinate product launches
· Identify appropriate market opportunities through synthesis of sound segmentation, targeting and positioning strategies and sales collateral
Qualifications:
Education:
· Bachelor’s degree required
· MBA or equivalent strongly preferred
Experience and Skills:
Required:
· Three years of marketing or related experience with at least two years of marketing experience in the medical device sector
· Ability to construct global marke...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-14 10:22:50
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Supply Operations
Job Category:
Professional
All Job Posting Locations:
CN027 Shanghai Gui Qing Rd
Job Description:
General Mission
The Clinical Supply Associate will manage clinical supplies for clinical trial execution in Asia-Pacific region.
He/she will be responsible for project planning and scheduling between internal stakeholders (clinical operation, supply chain, quality, et.al) and external stakeholders (clinical sites & CMOs).
The Clinical Supply Associate will be the point of contact for Clinical Operations and CMC activities related to advanced therapy treatment scheduling & triaging technical/operational issues during the whole chain.
This position will be based in Shanghai, China.
Specific Missions
• Close coordination with Clinical Operation team to understand site-based timings for new site initiations, planning, and leading of logistical test runs between Clinical Sites, CMO & MFG.
• Provides site and study level training related to patient onboarding and all aspects of supply chain.
• Set up the supply chain network across APAC region with a focus on advanced therapy.
Work closely with local/global teams to ensure the smooth and on-time delivery of supplies.
• For patients identified for participation in a clinical trial, coordinates & tracks the patient journey, triaging any issues to appropriate stakeholders between subject screening & IP receipt on site.
• Participates in GCP and GMP health authority inspections.
Have previous experience managing work with Contract Manufacturing Organizations to perform capability forecast and assessments, and provide expertise to influence and bridge gap analysis to meet Clinical Trial requirements.
Profile Needed for This Function
Knowledge
• Requires general supply chain managment experience in phamacieutical company with excellent project management and communication skills.
Experience with clinical trial operations, pharma/biotech R&D is preferred.
• Demonstrate ability and experience to work in a highly regulated environment (HA/J&J standards and guidelines, general GCP/GMP guidelines) is required.
• With some guidance, responsible for any tech support/use resolution at those internal or external stakeholders.
• Supports proactively in the continuous improvement of the overall supply chain processes.
• The abi...
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-05-14 10:22:08
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
Intégrer Johnson & Johnson Innovative Medecine, la division pharmaceutique du Groupe Johnson & Johnson, leader mondial dans le domaine de la santé (126500 collaborateurs dans le monde, 265 entreprises présentes dans 60 pays), c'est participer au développement de solutions thérapeutiques innovantes et partager notre volonté de changer la prise en charge médicale pour mieux répondre aux nouveaux enjeux de santé publique.
Rejoindre nos équipes, c'est s'épanouir dans une entreprise à taille humaine tout en bénéficiant des opportunités d'un grand groupe.
Nous travaillons pour que chacun puisse exprimer le meilleur de soi-même, afin de valoriser toutes les individualités.
Nous agissons en faveur de la diversité des talents qui nous rejoignent.
Ancrées dans notre Credo, la diversité et l’inclusion contribuent à valoriser le caractère unique de chacun de nos collaborateurs.
Johnson & Johnson est fier d'être un employeur qui prône l'égalité des chances.
Johnson & Johnson Innovative Medecine France recrute un analyste Business Intelligence en alternance
Contrat Alternance d’une durée de 12 mois - début en Septembre 2025
Localisation : Issy-Les-Moulineaux
Intégré au sein de l’équipe Business Intelligence, vous assisterez l’équipe Business Intelligence, dont les enjeux sont la compréhension fine de nos marchés et le pilotage de la performance de nos produits via des reportings clairs facilitant les prises de décision et la conduite d’études de marché.
Dans ce cadre, votre rôle sera :
* Accompagner les business analystes dans le suivi de la performance, et sur leurs besoins Ad Hoc : réalisation de brief études de marché, synthèse de veille concurrentielle, Cadrage et animations de workshop, …
* Être en support de l’équipe excellence opérationnelle dans la co-construction et la pérennisation de dashboard harmonisés sur les différentes aires thérapeutiques
* De former les équipes et jouer le rôle de modération sur notre plateforme de remontée d’insight.
Qualifications - External
Vous êtes actuellement étudiant en 3è cycle parcours scientifique, école de commerce, DESS, école d’ingénieurs, statisticien + 3e cycle marketing.
Vous possédez :
* u...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-05-14 10:20:44
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ERM is hiring a Safety Specialist onsite at a key client located in Sugarland, Texas.
In this critical role, you will be responsible for ensuring health and safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety is preserved.
The ideal candidate will bring working knowledge of H&S technical capability and deep understanding of business processes to help our clients proactively address their health and safety risks and challenges.
This is a full-time (40 hours a week) limited-term role, with a duration of 6-months, extendable.
RESPONSIBILITIES:
* Provide technical assistance on safety-related compliance projects; safety management system development and implementation; safety oversight, industrial hygiene monitoring; and safety auditing.
* Develop safety procedures, plans, permits, and reports.
* Assess regulatory compliance across various safety programs and environmental media.
* Perform compliance audits and implement follow-up corrective actions to ensure compliance with federal, state, and local regulations.
* Design and implement safety management systems and programs for clients.
* Provide on-site H&S compliance support at client facilities.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree.
Masters preferred.
* Minimum of 3 years’ relevant consulting experience in working with significant chemical, manufacturing or industrial clients on regulatory compliance and sustainable H&S compliance programs.
* Certification in field; ASP/CSP, CIH, PE, or similar registration highly desirable.
* Be passionate about safety performance improvement and have working experience with the following H&S topics:
o LOTO
o Confined space
o Hazard recognition
o Scaffolding
o Excavation
* Demonstrated ability to provide detailed regulatory interpretation of federal and state OSHA regulations.
* Excellent communication and interpersonal skills.
* MS Office Suite and database management for managing large volumes of data.
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-05-14 10:16:52
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ERM is hiring an Environmental Consultant onsite at a key client in Odessa, Texas.
In this role, you will provide project management and technical assistance on environmental compliance projects, environmental management systems, auditing, and compliance assurance programs.
This is a full-time (40 hours a week) limited-term role for a 6-month duration, extendable.
RESPONSIBILITIES:
* Provide air permitting support (gather equipment and production data, prepare application, route through review process & submit, review routinely to ensure production rates are adequate)
* Provide flaring support (calculate flaring emissions, maintain flaring/venting guidance for operations personnel)
* Participate in planning meetings with customer.
Gather equipment inventory and compile data.
* Provide technical assistance on air quality related compliance projects, auditing and air quality management system projects.
* Perform environment compliance audits and implement follow-up corrective actions to ensure compliance with federal, state, and local regulations.
* Assess regulatory compliance across various environmental programs and environmental media, including analyzing large volumes of data in spreadsheet and database formats.
* Support the development of environmental compliance registers which detail the applicable requirements for our clients' facilities and map them to compliance tasks.
* Support the development of environmental compliance and management system programs and policies for clients.
* Prepare plans, permits, and reports for client oil field waste, produced water, SPCC Plans, and chemical reporting programs.
* Provide on-site environmental compliance support at client facilities.
* Perform and manage multiple projects within scope/budget/schedule expectations and ensure quality standards on project deliverables.
* Support ERM Partners-in-Charge and other Project Managers to effectively manage and deliver projects.
* Effectively steward and build client relationships leading to repeat business.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* Bachelor's Degree in engineering, environmental science or related discipline preferred.
* A minimum of 3 years of EHS experience in consulting and/or industrial environments.
Oil & gas or chemical sector experience desired.
* Professional registrations/certifications are preferred, but not mandatory (PE, REM, CIH, ASP/CSP, CHMM).
* Strong knowledge of federal and state environmental regulations; experience in implementing programs in response to these regulations (e.g., as a consultant to industry), including Air Quality, SPCC Plans, SWPP Plans, EPCRA reporting, oil field and RCRA waste management requirements, etc.
* Excellent communication, interpersonal, MS Office computer, and analytical skills; experienced in writing comprehensive technical reports.
* Ability t...
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Type: Permanent Location: San Antonio, US-TX
Salary / Rate: Not Specified
Posted: 2025-05-14 10:16:50
-
ERM is hiring a Safety Specialist onsite at a key client located in Odessa, Texas.
In this critical role, you will be responsible for ensuring health and safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety is preserved.
The ideal candidate will bring working knowledge of H&S technical capability and deep understanding of business processes to help our clients proactively address their health and safety risks and challenges.
This is a full-time (40 hours a week) limited-term role, with a duration of 6-months, extendable.
RESPONSIBILITIES:
* Provide technical assistance on safety-related compliance projects; safety management system development and implementation; safety oversight, industrial hygiene monitoring; and safety auditing.
* Develop safety procedures, plans, permits, and reports.
* Assess regulatory compliance across various safety programs and environmental media.
* Perform compliance audits and implement follow-up corrective actions to ensure compliance with federal, state, and local regulations.
* Design and implement safety management systems and programs.
* Provide on-site H&S compliance support.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or a related degree.
Masters preferred.
* Minimum of 3 years’ relevant experience in working with chemical, manufacturing, or industrial companies on H&S compliance programs.
* Be passionate about safety performance improvement and have working experience with the H&S topics such as:
o LOTO
o Confined space
o Hazard recognition
o Scaffolding
o Excavation
* Demonstrated ability to provide detailed regulatory interpretation of federal and state OSHA regulations.
* Excellent communication and interpersonal skills.
* MS Office Suite and database management for managing large volumes of data.
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Type: Permanent Location: San Antonio, US-TX
Salary / Rate: Not Specified
Posted: 2025-05-14 10:16:49
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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!
Devenez notre futur(e) Technicien Logistique en horaire de journée CDI
Suite à une évolution de l’organisation du Magasin, nous recherchons un(e) Technicien Logistique, rattaché au responsable Logistique.
Venez rejoindre un site dynamique et à taille humaine ! Vos principales missions seront la gestion du stock et la gestion des déchets.
Dans ce cadre vous:
* Assurez la gestion du stock : historique, analyse des mouvements, ajustements éventuels;
* Assurez la justesse de l’inventaire tout au long de l’année
* Participez à l’inventaire annuel en partenariat avec la Finance
* Organisez la collecte des déchets au sein du site et leur expédition en partenariat avec le service HSE
* Etes responsable de l’expédition des colis (préparation, choix du transporteur, création des factures Proforma)
* Gérez les consommables (suivi des stocks, commandes)
* Vous êtes le back-up du Responsable Transport (expéditions avec sous-traitants, création documentaire)
Votre profil :
* Votre expérience en gestion de stocks recouvre au moins 2 ans
* Vous êtes à l’aise en Anglais (niveau B1)
* Vous maîtrisez SAP ou un autre ERP
* Vous disposez à minima d’une formation BUT ou Licence Pro Gestion logistique
Les plus qui feront la différence :
* Votre sens de l’organisation, votre rigueur et votre autonomie.
* Votre capacité d’adaptation et votre engagement seront particulièrement appréciés.
* Votre maîtrise des outils bureautiques.
* Votre motivation à participer à l’amélioration continue et à relever des challenges collectifs
Nous vous attendons !
A propos de Elanco
Groupe pharmaceutique international leader dans le développement de produits et services améliorant la santé des animaux de compagnie et de rente.
Le développement de Elanco est fondé sur des valeurs fortes et importantes qui sont : l’Intégrité, le Respect et l’Excellence.
Le site de Huningue, basé dans le Sud Alsace, a plus de 35 ans d’expé...
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Type: Permanent Location: Huningue Cedex, FR-68
Salary / Rate: 38000
Posted: 2025-05-13 08:17:04
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Are you ready to dive into the world of creative problem-solving? Are you up for exciting challenges and eager to expand your knowledge? If so, we have an incredible opportunity for you!
A vibrant division of Harris; Advanced Utility Systems' Client Services is on the lookout for a dynamic Technical Consultant who can deliver top-notch customer care.
As part of this role, you'll become a subject matter expert in our products through client training, troubleshooting issues, and addressing client requests.
But that's not all! You'll also get to flex your skills by effectively integrating functionalities in our CIS Infinity system and taking charge of multiple projects independently.
What's even better? You won't be alone in this journey.
You'll be collaborating closely with an amazing team to implement new enhancements and seamlessly integrate our web solutions with CIS Infinity.
If you're ready to take on this thrilling challenge and be part of an innovative team, we can't wait to hear from you! Let's embark on this exciting adventure together.
Apply now!
What your impact will be:
* Assess and translate client’s requests into what the client truly needs
* Find and implement creative and optimal solutions to accommodate the requirements within our applications
* Analyze and troubleshoot product stability inquiries or issues of both product and technical nature by phone or electronically through the ticketing system
* Liaise with 3rd party vendors, end-users, and our client’s IT
* Document configuration, enhancement, and testing notes for various projects through the ticketing system
* Work closely with other team members as part of a cohesive group on various projects
* Provide client training or assistance remotely or occasionally onsite
* Maximize and maintain current knowledge and awareness of applications and related technologies
What we are looking for:
* 2-5+ years of experience in customer support/business analyst
* Ability to review and analyze the following programming languages: VFP, C#, ASP.NET, and Powershell
* Ability to create and modify complex SQL scripts
* Ability to interpret requirements, and recommend solutions that best address clients' needs
* Ability to travel up to 25% in North America
* College Diploma in Computer Science or equivalent industry experience
* Excellent analytical, research and problem-solving skills
* Exceptional verbal and written communication skills
* Exceptional attention to detail and the ability to grasp concepts quickly
What would make you stand out:
* Experience with Remote Desktop Services/RemoteApp
* Experience with multiple remote access tools & techniques such as webex, remote desktop, VPN
* Oral or written communication in French
* Customer Service Training or Certification
* Experience in IT Support or Utility Billing or other financial applications
* Experience with Cr...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: 90000
Posted: 2025-05-13 08:17:01
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Come care with us at West Coast University! As a Physician Assistant Faculty member for a certified Great Place to Work, you will guide students to do more than change their own lives – you will help change the lives of every patient they treat throughout their career in healthcare. At West Coast University you will have the opportunity to share your success story with the next generation of Physician Assistant as a key member of our student-centered, innovative community!
You will make an impact by:
* Provides professional leadership and support, and serves as an educator, role model, mentor and facilitator.
* Create an educational environment which fosters innovation, responsiveness, and accountability
* Regularly contributes to improvement or upgrading of class materials and syllabi utilizing identified University processes
* Utilizes a variety of teaching methodologies to instruct students, always with intent to facilitate observable evidence of student fulfillment of prescribed learning outcomes.
* Demonstrates enthusiasm for teaching and the teaching/learning process and for individual students.
* Assists with assessment, critique and evaluation of overall curriculum and may lead the process of revisions to program and syllabi (if necessary) while ensuring quality.
Your Experience Includes:
* 0-4 years of teaching in a University (or College) setting or previous rank of assistant professor awarded by a regionally accredited institution.
* Teaching experience in Physician Assistant courses and initiated research interest focused on evidence-based clinical research is strongly preferred.
* Working with online learning management systems to further engage the student learning process desirable.
* Documented 3 years of experience as a practicing clinician
Education:
* Must provide a documented background in educational methodology consistent with teaching assignments including but not limited to education theory and practice, or current concepts relative to specific subjects he or she will be teaching, or current clinical practice experience, or distance education techniques and delivery.
* Terminal academic degree required (Master’s degree), doctorate preferred
LICENSES/CERTIFICATIONS:
* NCCPA certified Physician Assistant or Board certified (or eligible) allopathic or osteopathic physician
* PA license (or eligible) or MD / DO licensed or eligible for licensure
#LI-AM1
#HEJ
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Type: Permanent Location: Los Angeles, US-CA
Salary / Rate: 56.5
Posted: 2025-05-13 08:15:40
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
...
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Type: Permanent Location: De Pere, US-WI
Salary / Rate: Not Specified
Posted: 2025-05-13 08:15:18
-
PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
...
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Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2025-05-13 08:15:18
-
Your Job
INVISTA has an immediate need for a Research & Development Engineer at our Seaford, DE site.
The selected individual will be technology-driven and continually develop new capabilities consistent with innate abilities and evolving business needs.
Check out the following website for more information about our products: CORDURA® | Leisurewear, Activewear and Workwear
What You Will Do
* Deliver transformational innovation solutions against business problem statements that will advance INVISTA's competitive advantage and create superior long-term value for the business
* Apply curiosity, urgency, and a rapid experimentation mentality to design and conduct experiments against technical killer questions
* Rapidly evaluate ideas using advanced innovation principles and tools to focus on the critical few that will successfully drive business returns
* Apply root cause analysis and critical thinking to develop market insights and advance the integrated business point of view on market opportunities and risks
* Plan and execute laboratory and semi-works testing to evaluate the commercial viability of new transformational technologies
* Support technology scale-up and commercialization in global production facilities to drive successful product handoffs and operational excellence
* Create a sustainable and transformational competitive advantage for INVISTA through application of strong intellectual property (IP) capabilities leveraged across the nylon enterprise
* Stay abreast of the competitive landscape, including external polymer, fiber, textile and airbag innovations, to use as a source of insight and inspiration
* Build strong collaborative relationships with global cross-functional teams, including researchers, technicians, and manufacturing and business leaders
* Mentor and support coworkers to enhance their overall productivity and effectiveness
* Execute all responsibilities with excellence in EHS and compliance
* Apply the principles of Market-Based Management® in all aspects of work to create virtuous cycles of mutual benefit
Who You Are (Basic Qualifications)
* Bachelor's Degree or higher in Chemical Engineering, Polymer Science, or Material Science
* Three (3) or more years' of industrial research experience
* Experience with statistical and data analysis
What Will Put You Ahead
* Master's degree or higher in Engineering, Chemical, Material Science or related discipline
* Five (5) or more years' industrial experience in polymer processing, melt spinning, staple fiber production, or staple yarn spinning
* Five (5) or more years' experience textile engineering
* Applied knowledge or experience in textile and fiber applications
* Experience in research & development of a wide range of materials or polymers
* Experience in patent development and landscaping
At Koch companies, we are entrepreneurs.
This means we openly challeng...
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Type: Permanent Location: Seaford, US-DE
Salary / Rate: Not Specified
Posted: 2025-05-12 08:16:41
-
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 Assistant - Quality Control, Biochemistry
This role will be a laboratory-based position with the QC Biochemistry group responsible for a wide variety of biochemical assays.
This role will rely heavily on an ability to perform regular functions within a GMP environment and perform flawless lab work on high value projects.
Regular projects include release and stability testing, assay development, validation, training, technical writing, and regular use of specialized equipment/software.
Your Responsibilities
* Conducts a range of biochemical assays, encompassing both routine and non-routine testing, on various sample types including raw materials, in-process materials, finished goods, environmental monitoring samples, and stability samples.
This includes method development, execution, and troubleshooting.
* Prepares, reviews, and approves a variety of essential QC documentation, including test protocols, validation protocols, special outlines, reports, Certificates of Analysis (CoAs), out-of-specification/out-of-trend (OOS/OOT) investigation reports, and deviation reports.
* Ensures the QC laboratory operates in full compliance with current Good Manufacturing Practices (cGxP) guidelines, encompassing laboratory safety, performance standards, meticulous documentation practices, regular equipment maintenance, and adherence to environmental regulations.
* Generates, reviews, and approves analytical data to ensure accuracy, completeness, and regulatory compliance.
Investigates and documents any OOS/OOT results and deviations encountered during testing.
Validates new and revised testing methods and qualifies existing methodologies as needed.
* Serves as a subject matter expert (SME) and liaison between the QC department and other internal departments, external vendors, and contractors.
Provides training to other analysts on laboratory procedures and assays, and stays current with the latest analytical techniques and best practices through continuing education and software proficiency.
Participates in internal assessm...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 31.93
Posted: 2025-05-12 08:14:29
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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:
Beijing, 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% in compliance.
Stra...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-12 08:10:24
