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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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The Customer Success Manager (CSM) is an education-focused professional whose primary role is to train, foster and build relationships by serving as the first point of contact for customers; ensuring retention, while supporting customers’ needs.
This position works collaboratively with the Sales & Marketing, Instructional, Product Development, and other internal teams to ensure continuity of service.
The CSM will hold the record of all Service Level Agreements (SLAs) and act as an advocate to existing and future customers to ensure a seamless transition post-sale, customer retention year over year, and ensure that the Edison model is effectively implemented.
The CSM will work closely to the assigned Sales Professional on securing the renewal of contracts.
Essential Duties and Responsibilities:
Customer Service and Retention
* Serve as the first and primary point of contact for customers
* Train and onboard new clients through the prepared implementation process
* Train existing customers in new features as they are released
* Train existing customers as they assign new contacts or expand usage
* Answer all incoming communication from customers and troubleshoot any issues
* Build relationships by providing consistent value and fostering customer loyalty
* Develop relationships with key stakeholders and maintain a focus on business development from customer onboarding through renewal in joint communication with assigned Sales personnel
* Maintain a record of Service Level Agreements for all customers to ensure proper program implementation through Hubspot
* Demonstrate product to interested leads
* Travel to visit clients or attend conference/trade shows as needed to guarantee customer success
* Speak and present at trade shows and conferences as needed
* Effectively leverage customer feedback via annual Net Promoter Survey (NPS) results; follow up with all district “Detractors” and develop written mitigation plans/timeframes to address pain points
* Demonstrate specific understanding of individual district needs to determine solutions that benefit both the customer and our organization
* Organize and facilitate monthly district achievement meetings to ensure understanding of the needs of the customer’s program; drive high levels of customer satisfaction through consultative recommendations (
*note: this is in lieu of the bullet point that cites “Attend regular meetings…)
* Understand and proactively communicate student outcomes and recommend mitigation strategies to effectively address
* Review district dashboard data on a weekly basis and ensure corresponding and tailored district outreach
* Consistently engage with and uncover the ‘Whys?’ behind district feedback
* Communicate all product enhancements, technological updates, and other pertinent information to districts in a timely, efficient manner
* and professionally
* Regula...
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Type: Permanent Location: Springfield, US-IL
Salary / Rate: 52500
Posted: 2025-05-14 12:36:55
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PURPOSE AND SCOPE:
Conduct routine laboratory tests, in support of manufacturing operations.
Analyzes and records test data to monitor and maintain conformity to specifications.
Performs duties in alignment with Test Methods (TM), Standard Operating Procedures (SOP), current Good Manufacturing Practices (cGMP), and Good Laboratory Practices (GLP).
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Under general supervision, follows established company policies and procedures and applies acquired job skills to
Set up lab equipment and instrumentation required for tests, research, or process control.
* Responsible to perform daily analytical tests according to applicable test methods/procedures.
* Responsible for the precision, accuracy and quality of work product.
* Document results of test and analyses.
* Maintain laboratory equipment through daily cleaning and consistent with PMs.
* Responsible for the cleanliness of the work environment
* Maintain general housekeeping of working area and plant.
* Performs functions that require full knowledge of general aspects of the job.
* Works on assignments that are semi-routine in nature, but recognizes the need for occasional deviation from accepted practice.
* Contacts are typically with individuals within own department and occasionally with contacts outside own organization. Contacts involve obtaining or providing information or data requiring some explanation or interpretation.
* May refer to senior level staff for assistance with higher level problems that may arise.
* Escalates issues to supervisor for resolution, as deemed necessary.
* Follow all Fresenius Policies.
* Regular attendance and maintaining a good attendance record is an essential function of the job.
* Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations.
* Assist with various projects as assigned by direct supervisor.
* Other duties as assigned.
Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.
PHYSICAL DEMANDS AND WORKING CONDITIONS:
* The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
* While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear; taste or smell and Personal Protective Equipment required may include: safety glasses.
The employee must frequently lift and/or move up to 50 pounds and occasional...
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Type: Permanent Location: Knoxville, US-TN
Salary / Rate: Not Specified
Posted: 2025-05-14 12:34:17
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PURPOSE AND SCOPE:
Conduct routine laboratory tests, in support of manufacturing operations.
Analyzes and records test data to monitor and maintain conformity to specifications.
Performs duties in alignment with Test Methods (TM), Standard Operating Procedures (SOP), current Good Manufacturing Practices (cGMP), and Good Laboratory Practices (GLP).
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Under general supervision, follows established company policies and procedures and applies acquired job skills to
Set up lab equipment and instrumentation required for tests, research, or process control.
* Responsible to perform daily analytical tests according to applicable test methods/procedures.
* Responsible for the precision, accuracy and quality of work product.
* Document results of test and analyses.
* Maintain laboratory equipment through daily cleaning and consistent with PMs.
* Responsible for the cleanliness of the work environment
* Maintain general housekeeping of working area and plant.
* Performs functions that require full knowledge of general aspects of the job.
* Works on assignments that are semi-routine in nature, but recognizes the need for occasional deviation from accepted practice.
* Contacts are typically with individuals within own department and occasionally with contacts outside own organization. Contacts involve obtaining or providing information or data requiring some explanation or interpretation.
* May refer to senior level staff for assistance with higher level problems that may arise.
* Escalates issues to supervisor for resolution, as deemed necessary.
* Follow all Fresenius Policies.
* Regular attendance and maintaining a good attendance record is an essential function of the job.
* Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations.
* Assist with various projects as assigned by direct supervisor.
* Other duties as assigned.
Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.
PHYSICAL DEMANDS AND WORKING CONDITIONS:
* The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
* While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear; taste or smell and Personal Protective Equipment required may include: safety glasses.
The employee must frequently lift and/or move up to 50 pounds and occasional...
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Type: Permanent Location: Knoxville, US-TN
Salary / Rate: Not Specified
Posted: 2025-05-14 12:34:07
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Senior Manager – Competitive Intelligence
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:
The Senior Manager - Competitive Intelligence, is a critical leadership role within the Ideal Consumer Experience team, part of the broader Product Steward Team in Global R&E.
The individual will be responsible for advancing Kimberly-Clark’s competitive intelligence, benchmarking, and consumer-relevant product insights capabilities to enable informed decision-making in innovation, claims development, design to value strategies, cost optimization, and strategic planning.
The Senior Manager will ensure Intelligence and Competitive Fitness insights are integrated early and consistently across the innovation pipeline, connecting with Innovation Capability Teams (ICTs), the Global Growth Organization (GGO), Value Stream Teams and Global R&E leadership to drive strategic foresight that shape product development, strengthen consumer benefits, and unlock competitive advantage in the marketplace.
Scope:
The Competitive Fitness team has been purpose-driven to meet critical enterprise needs — including understanding the evolving competitive landscape, identifying design to value opportunities, and informing the positioning of Kimberly-Clark brands for long-term success.
As the team continues to expand its strategic impact, the Senior Manager will lead efforts to evolve Competitive Fitness into a proactive, globally harmonized capability that translates market signals, product trends, and technical benchmarking into actionable opportunities for product innovation, consumer benefit differentiation, and margin improvement.
This role is central to ensuring Competitive Fitness delivers impact across the broader Product Steward and Ideal Consumer Experience teams and informs decisions within innovation roadmaps, claims strategy, and portfolio planning.
Key Responsibilities:
* Set and lead the Competitive Fitness strategy, ensuring it aligns with enterprise priorities, ICT roadmaps, and product development needs.
* Lead a team of up to ten direct reports.
* Deliver integrated competitive insights by analyzing product performance, material choices, claims strategies, and consumer preferences across the market landscape.
* Use competitive fitness inputs to inform and direct innovation teams toward opportunities for new product and material development, differentiated consumer benefits, and improved value propositions.
* Identify design to value opportunities based on materi...
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Type: Permanent Location: Irving, US-TX
Salary / Rate: Not Specified
Posted: 2025-05-14 12:31:45
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Financial Planning and Analysis Specialist
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 be supporting an organization’s financial strategy by providing data-driven insights, recommendations and overall business planning.
Here are some key responsibilities and functions required for the position:
* Performance Analysis: Analyze financial performance by comparing actual results with forecasts and identifying trends, variances, and areas for improvement.
* Budgeting and Forecasting: Developing and maintaining financial plans and forecasts to align with the company’s strategic goals.
* Reporting: Preparing and presenting monthly, quarterly, and annual financial reports to management; Financial Modeling: Creating financial models to support strategic initiatives and decision-making.
* KPI Monitoring: Tracking key performance indicators (KPIs) related to sales, costs, expenses, and profit margins.
* Scenario Analysis: Conducting scenario and sensitivity analyses to forecast potential outcomes and impacts on the business.
* Strategic Support: Providing data-driven insights and recommendations to support strategic planning and operational decisions.
About Us
Huggies®.
Intimus®.
Poise®.
Plenitud®.
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 makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business.
In one o...
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Type: Permanent Location: Sao Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-05-14 12:31:17
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States
Job Description:
We are searching for the best talent for Account Executive, AHH to be in Cleveland, OH.
About Surgery
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world.
Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer.
Patients are waiting.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Ethicon has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures.
Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives.
Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact.
For more information, visit www.ethicon.com.
The Account Executive- Advanced Hemostasis and Healing will:
* Own the full bag of Ethicon offerings of comprehensive surgical devices and solutions including the hemostasis, energy sealing and dissection, surgical stapling and wound closure platforms. The Account Executive – AHH will have a focus on growing our hemostasis and wound closure platforms
* With a platform focus, Account Executives will sell surgical solutions to surgeons and hospital decision makers, primarily in an operating room setting.
* Be assigned a sales territory focusing on assigned physicians and hospital Institutions.
* Be accountable to attain the forecast in their assigned accounts / territory.
* Have ...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-14 10:22:52
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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:
Career Programs
Job Sub Function:
Post Doc – R&D Product Development
Job Category:
Career Program
All Job Posting Locations:
Jacksonville, Florida, United States of America
Job Description:
We are searching for the best talent for a Clinical Science Post Doctoral Fellow to join our Vision Team located in Jacksonville, FL.
This is a two year duration based role.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
You will be responsible for:
* Design, conduct, and interpret clinical research studies in support of new product introduction.
* Contribute in the origination or direction of experiments through the development of methodologies.
* Review, analyze, and interpret data, and draw conclusions which lead to planning further research.
* Summarize and interpret clinical study data in technical reports.
* Communicate clinical study results and conclusions to cross-function teams using appropriate interpretation and understanding of clinical outcomes related to product performance.
* Keep ahead of changing and emerging industry, business, and technical trends and competitive product offerings to influence R&D to improve products, processes, and services.
* Seek out and build relationships with new and existing external subject matter experts to develop solutions to project problems and clinical research approaches including development of new test methods.
* Be recognized as a subject matter expert on contact lenses and clinical research at JJVC.
* Adhere to environmental policy, procedures, and support department environmental objectives.
* Engage in Credo-based decision-making.
* Provide input...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2025-05-14 10:22:44
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Risk Management
Job Category:
Professional
All Job Posting Locations:
Guaynabo, Puerto Rico, United States of America, Horsham, Pennsylvania, United States of America, Jacksonville, Florida, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Tampa, Florida, United States of America, Titusville, New Jersey, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
Johnson & Johnson is currently seeking a Global Services Finance (GSF) A&D Compliance Manager to join our Acquisition & Divestiture (A&D) Compliance team located in New Brunswick, NJ or Tampa, FL.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
As the Global Services Acquisition and Divestiture Compliance Manager, he/she will be responsible to provide strong leadership and oversight within the execution of the Finance compliance integration activities supporting the Intra-Cellular business align to Johnson & Johnson standards across all relevant financial cycles.
The role will also partner very closely with the Intra-Cellular finance leadership team, Acquisition and Divestiture Operations Finance/PMO, Global Audit & Assurance (GAA), and external auditors.
The role will report directly to the GSF Compliance Director – Innovative Medicine and A&D.
Key Responsibilities:
Effective Risk Management execution through minimization of financial and operational risks associated with the internal control environment, along with the assessment, design, and implementation of internal controls by providing recommendations for continuous process and control improvements.
This includes:
* Managing audit support optimally through strong partnerships with business unit finance, internal audit team, and external auditors to ensure control standards are upheld.
This includes coordination of internal and/or external audits and advising remediation efforts for exceptions identified.
* Advise and consult business process owners on control requirement expectations and related execution across the various workstreams (e.g.
Revenue, Inventory, Rebates, etc.) to build and maintain a strong internal control environment for acquired or divested businesses.
This includes supporting A&D integration activities related ...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-14 10:22:33
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Über Innovative Medizin
Unsere Expertise in innovativer Medizin wird von Patienten beeinflusst und inspiriert, deren Erkenntnisse unsere wissenschaftlich fundierten Fortschritte fördern.
Visionäre wie Sie arbeiten an Teams, die Leben retten, indem sie Medikamente von morgen entwickeln.
Begleiten Sie uns auf unserem Weg, während wir Therapien weiterentwickeln, Heilmitteln finden und den Übergang von der Forschung ins echte Leben ermöglichen, immer im engen Austausch mit unseren Patienten, um sie bei jedem Schritt zu unterstützen.
Weitere Informationen finden Sie unter https://www.jnj.com/innovative-medicine
Wir suchen das beste Talent für die Position des/der QC Microbiology Specialist (Schwerpunkt QC Micro oversight) in Schaffhausen.
Der Zweck dieser Position ist die Sicherstellung und Optimierung der Qualität in mikrobiologischen Prozessen, um die Einhaltung von GMP-Vorgaben und die Minimierung von Qualitätsproblemen in der aseptischen Herstellung zu gewährleisten.
Ihre Aufgaben & Verantwortlichkeiten:
* Optimierung und Weiterentwicklung unserer Dokumentations- und Laborsysteme hinsichtlich Vermeidung von Quality Issues.
* Oversight von Produktionsprozessen im Schichtbetrieb
* Training von Produktionsmitarbeitern im Aufgabenbereich
* Unterstützung bei Projektarbeiten, z.B.
Abschluss von CAPAs
* Unterstützung bei der Erstellung von risk assessments
* Erstellung und Kontrolle von Trainingsdokumenten, sowie Erstellen von SOPs und Arbeitsanweisungen im Aufgabenbereich.
* Unterstützung bei der Bearbeitung von Abweichungen sowie Festlegung korrigierender Massnahmen im Aufgabenbereich.
* Unterstützung in Behördeninspektionen und Kundenaudits
* Erstellung von GMP Dokumenten
* Unterstützung der termin- und GMP-gerechten Ausführung der Validierung von mikrobiologischen Methoden
* Mithilfe bei der Durchführung von organisatorischen und administrativen Aufgaben im Laborbereich.
* Einhalten der GMP-Vorgaben und Richtlinien.
* Arbeiten entsprechend cGMP, interner Vorschriften (SOPs) und externer Richtlinien.
* Sie arbeiten im 3-Schichtmodell
Ihr Qualifikationsportfolio & unsere Anforderungen:
Sie haben Mikrobiologiekenntnisse oder Produktionskenntnisse bei der aseptischen He...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-05-14 10:22:27
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Budapest, Hungary
Job Description:
Position Summary:
A Lead Local Trial Manager is considered as a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience.
This role is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries.
The Lead Local Trial Manager is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents.
The Lead Local Trial Manager is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements.
The Lead Local Trial Manager actively leads or contributes to process improvement; training and mentoring of other LTMs and Site Managers (SM).
The Lead Local Trial Manager may also perform the role of Trial Delivery Manager (TDM)/Trial Delivery Leader (TDL) for single country as described in GCO procedural documents.
Principal Responsibilities:
* May be delegated by Functional Manager (FM)/Clinical Research Manager (CRM) to lead country protocol feasibility (if applicable) and site feasibility assessment in conjunction with CTA (if applicable), SM and TDM/TDL.
Implements any local criteria for site selection.
Ensure consistent conduct of Site Qualification Visits and instruct teams on appropriate follow-up of Site Qualification Visit report and country feasibility report.
Recommends suitable sites for selection to participate in trial.
* Collaborates with the Program Delivery Leader (PDL), TDM/TDL, local management/Country Head and other study team member to select final site list.
* Contributes input to the study management documents at a country level or initiates development of these documents for a single country trial, as per SOPs.
May be delegated by study team to initiate document development for global/regional studies.
* Leads and coordinates local trial team activities in compliance...
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Type: Permanent Location: Budapest, HU-BU
Salary / Rate: Not Specified
Posted: 2025-05-14 10:21:43
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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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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Principal Clinical Research Associate – Shockwave Medical (Remote) to join our team.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Principal Clinical Research Associate (CRA) is responsible for the day-to-day management of a global clinical study.
The Principal CRA will be accountable for project management activities, oversight of multiple vendors and for conducting a global clinical study in compliance with applicable clinical and regulatory standards and in alignment with the business needs.
The individual is a subject matter expert in clinical research and this work is accomplished with minimal oversight, requires frequent contact with internal and external customers and is critical to the success of the business.
Essential Job Functions
* Responsible for organizing, communicating and evaluating team objectives for clinical studies.
* Participates in study design and study preparation activities, as applicable.
* Develops and revises clinical trial documentation including clinical trial protocol development, case report form (CRF) development, IRB/Ethics submissions.
* ...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-14 10:19:53
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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:
Sales Enablement
Job Sub Function:
Sales Operations & Administration
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Sr.
Sales Operations Analyst- Shockwave Medical- Remote to join our team.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
Shockwave Medical is looking for a Senior Sales Operations Analyst to join its world class team.
This role is responsible for analyzing complex data, generating both conclusions and recommendations, and effectively communicating those to decision-makers. The current environment is best suited for someone with a passion for improving existing processes and who has the ability to juggle multiple priorities in a fast-paced growing organization. In this role, you’ll be working with commercial leaders to drive data-based decisions and implement solutions to improve commercial performance.
Essential Job Functions
Analysis & Reporting
* Interpret, self-direct, and prioritize execution of incoming requests for analysis projects.
* Conduct analyses, develop conclusions & communicate recommendations to Sales, Marketing, Operations, and Finance.
* Create, monitor, support and oversee reports and dashboards in Excel, Salesforce, and PowerBI.
* Work with large d...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-14 10:19:46
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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
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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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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
This is an opportunity for you to bring your wealth of experience to the team and help shape the future of sustainability with world-changing innovations and low carbon technologies.
You have the power to shape things to make them better.
About the Role:
Are you seeking a role where you can make a difference and positively use your influencing skills and networks to foster change and help grow our business?
We are currently seeking an Occupational Hygienist for a permanent full-time opportunity based at our Kwinana Refinery reporting directly to the Health and Safety Manager.
The working roster is Monday to Friday, with one leisure day off every four-week period!
You will be working in a team environment, with support, training, and going career development, and you will be offered the opportunity to work across a wide scope of responsibilities and get experience in all areas of occupational Hygiene.
Your accountability extends to ensuring all people on site have an appropriate level of understanding of the potential hazards, control measures, and provide the latest relevant research to them minimise the risk to their health.
You will directly oversee the locations Fit Testing program and hold the statutory position of surface ventilation and noise officer.
Key responsibilities include:
* Maintain the site's established Health and Hygiene Management Plan.
* Facilitate ongoing monitoring of physical (e.g., noise, radiation) and chemical (e.g., dust, fumes) hazards in the workplace, ensuring appropriate data collection and analysis.
* Analyse monitoring results against relevant health standards and regulatory requirements, providing clear and actionable feedback to operating centres regarding routine findings and their potential impact on worker health.
* Manage the systematic collection and secure storage of occupational hygiene data, leveraging current technology to build a robust foundation for future epidemiological studies and trend analysis.
* Undertake and regularly update hazardous material risk assessments by reviewing all materials before purchase, maintaining a comprehensive digital register, and delivering thorough training on safe handling and use.
* Create and manage a comprehensive Respiratory Protection Program, ensuring adequate training on proper use, maintenance, and potential respiratory hazards, while continuously evaluating and implementing improved protective equipment.
What’s on offer:
* Career development opportunities to pursue your passion
* Monthly Leisure Day
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportuniti...
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Type: Permanent Location: KWINANA, AU-WA
Salary / Rate: Not Specified
Posted: 2025-05-13 08:16:59
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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
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Type: Permanent Location: Los Angeles, US-CA
Salary / Rate: 56.5
Posted: 2025-05-13 08:15:40
