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About the Family: We have been family-owned since 1908 and treat customers, patients, and employees like family.
It drives our unique connection with health care professionals, and it’s what makes their success our success.
For us it’s personal listening, advising, supporting, and celebrating them as we pursue a shared vision to help the world look better, feel better and live better.
We are a leading, global aesthetics business, and our award-winning portfolio of injectables, devices and skin care products help health care professionals fuel confidence through aesthetic medicine.
Key Responsibilities
Product Labeling Process:
* Manage the processing of all product labeling through the collaboration / review process, uploading attachments if needed, and ensuring final document meets standards for Document Control and applicable Labeling standards prior to release.
* Responsible for communicating document translations to the approved translation vendor(s) and ensuring they are appropriately released into the eQMS for applicable document revisions.
* Generating new InfoCards in the eQMS for Labels upon request.
* Own competency training for individuals required to review any labeling.
* Generate and/or review Quality Management System procedures.
* Proofread various documents to verify accuracy.
* Quality lead on new labeling projects.
* Implement new quality improvement initiatives / projects in accordance with cGMP expectations to improve compliance, quality levels and improve operational efficiencies.
New Markets Activities
* Lead New Markets activities by reviewing, approving, and processing applicable labeling requirements.
Standards
* Assist with adherence to all Federal, State, and Local regulations as they apply to manufacture/distribution of medical devices, pharmaceuticals, OTC, and cosmetics.
NCR and CAPA
* Lead corrective/preventive actions and product non-conformance including capturing data and investigations associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
Inspections
* Support with federal, state, and local regulatory officials during regulatory inspections.
* Support in internal and vendor quality system audits as applicable.
Other Duties as Assigned
* Provides support to Quality Management personnel and performs other duties as assigned.
Education:
* Bachelor’s Degree.
Required
* BS/BA in Physical Science or Engineering.
Preferred
Experience:
* 2 years in Medical Device or similar experience.
Required
* 2 years in a quality role.
Preferred
* ASQ Certification as a Quality Engineer or equivalent.
Preferred
Knowledge Skills and Abilities:
* Operate Personal Computer, copying machines, printers, and scanners.
Required
* Knowledge of quality systems, quality techniq...
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Type: Permanent Location: Racine, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-19 09:47:20
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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 / Key and Responsibilities:
* To lead swine technical service activities, guiding Key Account Customers, distributors to increase penetration of swine products
* To lead swine/ruminant products’ technical service activities in coordination with peer Technical Consultants, guiding Key Account Customers, distributors to increase penetration of swine/ruminant products
* Visiting key account farms and distributor key customers including product introduction, technical training, technical consultancy
* Carry out marketing trials with farms including demand evaluation, protocol designing, trial follow-up, report writing
* Carry out product trials with universities/institutes including protocol building, trial follow-up, report writing
* Update technical information for swine/ruminant (vaccine/medication program, diseases…); and work with experts (researchers, lecturers, suppliers, independent consultants)
* Conduct and deploy the technical service of Elanco (farm diagnosis, explaining the lab analysis result, develop new application…)
* Design content for promotional materials such as brochures, leaflets, posters, etc.
* Responsible for reviewing and approving technical and product content.
* Implement EKS (LLS, LOW, etc.) to enhance customer service, including implementation, training, analysis and interpretation of results.
* Be speaker at workshops, conferences and staff training.
* Work closely with Swine/Ruminant Product Manager and Sales Managers to align with marketing & technical strategies for each product
* Report to Technical Manager
* Ensuring of myself and my subordinates (if any) comply with the company rules and regulations including Ethics and Compliance and external laws and regulations.
Minimum Qualification (education, experience and/or training, required certifications):
* University degree in Veterinary Medicine.
* Fluent in English (both written and spoken)
* At least 2 year in swine farm experience.
* Minimum 3-5 years of...
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Type: Permanent Location: Ha Noi, VN-HN
Salary / Rate: Not Specified
Posted: 2025-04-19 08:48:04
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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: Sr.
Analytical Scientist, Biologics
As an Sr.
Analytical Scientist, Biologics you will be part of Elanco’s R&D team, driving the development of chromatographic, electrophoretic, and LC/MS analytical methods for biopharmaceutical products.
In this role, you’ll be responsible for advancing analytical techniques for therapeutic proteins and vaccines, supporting bioprocesses, and leading method development, validation, and transfer efforts across global sites.
If you are passionate about advancing analytical methodologies and playing a key role in biopharmaceutical development, we invite you to apply and join our innovative team!
Your Responsibilities:
* Develop and optimize chromatographic, electrophoretic, and LC/MS analytical methods for vaccine and therapeutic protein products.
* Innovate and implement analytical solutions for diverse drug formulations and bioprocess support.
* Lead method validation, verification, and transfer activities across global sites and CROs.
* Train and mentor associates and scientists globally to ensure consistency in analytical practices.
* Author technical reports, review scientific documents, and maintain laboratory safety standards.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree with 12+ years or Master’s Degree with 10+ years of experience in Analytical Chemistry, Biochemistry, Biophysics, or a related scientific field.
* Experience: Extensive hands-on experience developing HPLC/UPLC-based, electrophoretic, and LC/MS analytical methods for large molecule characterization.
* Top 2 skills: Strong expertise in analytical method development and validation, with excellent problem-solving and communication skills.
What will give you a competitive edge (preferred qualifications):
* Expertise in recombinant proteins, monoclonal antibodies, oligonucleotides, and peptides.
* Experience with method validation, transfer, and qualification under GMP conditions.
* Strong statistical knowledge and proficiency with statistica...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 123500
Posted: 2025-04-19 08:47:57
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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 Master Data Consultant
As a Quality Master Data Consultant, you will be part of our Global Master Data team, ensuring best-in-class data governance, process standardization, and optimization of SAP master data.
In this role, you’ll lead a team of analysts, execute master data maintenance, resolve quality management (QM) and vendor master data issues, and drive continuous improvement efforts.
Your focus will be on enhancing data integrity, system capabilities, and business efficiencies.
Your Responsibilities:
* Lead the execution and governance of master data maintenance within SAP and related systems.
* Manage and resolve QM object data issues while ensuring compliance with Standard Operating Procedures (SOPs).
* Assess the impact of data changes and ensure consistency across global business units.
* Identify and lead process improvement initiatives, including troubleshooting SAP execution issues and implementing solutions.
* Support global Quality Master Data Management initiatives, participating in power user forums and knowledge-sharing efforts.
* Drive standardization of data-related processes to enhance organizational efficiency and value.
* Support system releases, scope changes, and process enhancements in SAP.
* Provide transparent reporting and recommendations to leadership to improve data accuracy and compliance.
* Promote SAP as the single source of truth for master data while ensuring proper training and adoption across teams.'
What You Need to Succeed (Minimum Qualifications):
* Education: Bachelor’s degree in a scientific field (quality assurance, computer systems) or equivalent experience.
* Experience: 8+ years of experience as a compliance expert in and ERP within a related industry, specializing in quality and data management.
* Strong knowledge of ERP software, preferably SAP.
* Proven ability to analyze, anticipate, and resolve complex technical and business-related issues.
What Will Give You a Competitive Edge (Preferred Qualifications):
...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 135000
Posted: 2025-04-19 08:47:51
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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 Laboratory Technician
Quality Control Laboratory Technician, Microbiology will report to the QC Supervisor, Microbiology or equivalent.
This position will conduct routine and non-routine microbiology analysis and environmental monitoring.
In addition to, monitoring utilities and maintaining microbiology inventory, etc.
Your Responsibilities:
* Conduct routine and non-routine Microbiology based analysis of raw materials, in-process materials, finished goods, and stability samples; and conduct microbiology testing to include total organic carbon, conductivity, endotoxin, bioburden, growth promotion, mycoplasma, sterility, microbial identifications, gram stains, and personnel sampling.
* Perform routine and non-routine environmental monitoring (air viable, air non-viable, and surface sampling) of manufacturing environments and perform monitoring of utilities to include WFI, USP Water, Pure Steam, and Clean Compressed Air.
* Execute gowning qualification personnel performing activities in classified sterile environments as well as achieve and maintain gown qualification for sterile environments.
* Provide production support and participate in production fills and aseptic process simulations, and support equipment validation, calibration, and maintenance.
* Participate in internal assessments and audits as required, generate and report accurate data that meet regulatory compliance and ensure the QC lab is held to cGMP, safety, and environmental standards; and maintain QC Microbiology inventory, perform daily temperature checks on necessary equipment, and perform weekly cleaning of laboratory spaces.
* Assist in preparation of Certificates of Analyses, OOS/OOT Investigations, EM and Facility Investigations, and Deviations during testing; developing and qualifying/validating new testing methods and method transfers; write and revise testing methods; the development of specifications and justification of specifications; the preparation of QC standard operating procedures and forms; the preparati...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 30
Posted: 2025-04-19 08:47:49
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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!
Your Role: Quality Control /Environmental Monitoring Technician
Environmental Monitoring / QC Technician Microbiology will report to the QC Supervisor, Microbiology or equivalent.
This position will conduct routine and non-routine environmental monitoring of the manufacturing facilities and associated utilities, as well as microbiology analysis.
Your Responsibilities:
* Perform routine and non-routine environmental monitoring (air viable, air non-viable, and surface sampling) of manufacturing environments and perform monitoring of utilities to include WFI, USP Water, Pure Steam, and Clean Compressed Air.
* Execute gowning qualification personnel performing activities in classified sterile environments as well as achieve and maintain gown qualification for sterile environments.
* Ensure the QC lab is held to cGMP, safety, and environmental standards as well as generate and report accurate data that meet regulatory compliance, support equipment validation, calibration, and maintenance; and participate in internal assessments and audits as required.
* Conduct routine and non-routine Microbiology based analysis of raw materials, in-process materials, finished goods, and stability samples; and conduct microbiology testing to include total organic carbon, conductivity, endotoxin, bioburden, growth promotion, mycoplasma, sterility, microbial identifications, gram stains, and personnel sampling.
* Assist in preparation of Certificates of Analyses, OOS/OOT Investigations, EM and Facility Investigations, and Deviations during testing. Assist in developing and qualifying/validating new testing methods and method transfers.
Write and revise testing methods. Assist in the development of specifications and justification of specifications. Assist in the preparation of QC standard operating procedures and forms. Assist in preparation of QC method validation protocols/reports and other analytical study reports. Assist in the recommendation of new technologies and methods.
* Maintain QC Microbiology inv...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 28
Posted: 2025-04-19 08:47:47
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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.
We are seeking a Product Developer - Retail Tissue to help us extend an ideal balance of softness & strength® in our Angel Soft® bath tissue products at our Technical Center in Neenah, Wisconsin.
Our product developers represent the needs and desires of our consumers to design, manufacture, and deliver advantaged products.
As a product developer, you will have the unique opportunity to deepen your technical expertise in product design, leverage your creativity to tackle challenging problems, and apply a consumer-centric lens to delivering innovation.
Our Team
The Georgia-Pacific Angel Soft® retail bath tissue product development team leads the technical development of our Angel Soft® bath tissue products.
We are entrepreneurs who innovate daily and collaborate cross-functionally to design products and execute projects that create value for our consumers, customers, communities, and company.
We value lifelong learners who want to contribute and grow with us.
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
* Collaboration: Work with other product developers, business stakeholders, consumer research, quality, operations, and our technology platforms to drive year-over-year product, performance, and cost improvements.
* Consumer Focus: Connect consumer and market needs to product performance to develop and test alternatives and set technical specifications on product design.
* Design and Experimentation: Design, experiment, evaluate, and execute alternatives to test new product designs and hypotheses, including leading product trials on our pilot and production manufacturing equipment.
Analyze data sets using advanced statistical methods and data analysis tools to support strategic decision-making.
* Product Support: Provide technical support on product specifications, product claims, data substantiation, intellectual property, and overall product points of view to our business teams and other capability partners.
Who You Are (Basic Qualifications)
* Bachelor's degree or higher in paper science, engineering or physical science or at least 3 years of product development experience in paper products.
* Experience working in an R&D, product development, OR manufacturing environment independently leading technical projects or experiments, product development activities, and scaling up to commercial feasibility.
* Technical knowledge of papermaking and converting.
* Able and willing to travel an average of 25%.
What Will Put You Ahead
* Advanced...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-19 08:43:51
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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:
Strategy & Corporate Development
Job Sub Function:
Digital Strategy & Deployment
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Geel, Antwerp, Belgium, Latina, Italy, Leiden, South Holland, Netherlands, Ringaskiddy, Cork, Ireland
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson is recruiting for a Global Lead of Automation, based in a J&J manufacturing site in Athens GA, Gurabo PR, Cork IR, Leiden NL, Beerse/Geel BE, Schaffhausen CH, or Latina IT. This position is required to be on site 3 days per week.
Position Summary:
The Global Lead of Automation is a critical leadership role responsible for transforming the organization’s automation capabilities, infrastructure, and skills to a new level of excellence.
The role requires a strategic thinker who can move the needle in areas such as Process Control, robotics, and intelligent automation to drive operational efficiency and innovation.
Key Responsibilities:
* Develop and execute a comprehensive automation strategy that aligns with the company’s overall business objectives and drives competitive advantage in the marketplace.
* Foster a culture of innovation and continuous improvement in automation practices, ensuring alignment with emerging technologies and industry trends.
* Champion the development and implementation of advanced Manufacturing Process Control Systems and other automation tools to streamline processes and enhance productivity, adaptability and agility.
* Establish standardized solutions and governance frameworks across all global sites to ensure consistency, efficiency, effectiveness and compliance across all nodes, in line with site and Supply Chain strategies
* Lead and oversee the implementation of the Assets Management Framework and maturity roadmaps for automation.
* Lead the transformation of automation skills and infrastructure, enhancing the organization’s ability to leverage advanced technologies, including AI, machine learning, and IoT,...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-19 08:26:31
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Strategy & Corporate Development
Job Sub Function:
Digital Strategy & Deployment
Job Category:
People Leader
All Job Posting Locations:
Athens, Georgia, United States of America, Gurabo, Puerto Rico, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson is recruiting for a Global Lead of Automation, based in a J&J manufacturing site in Athens GA, Gurabo PR, Cork IR, Leiden NL, Beerse/Geel BE, Schaffhausen CH, or Latina IT. This position is required to be on site 3 days per week.
Position Summary:
The Global Lead of Automation is a critical leadership role responsible for transforming the organization’s automation capabilities, infrastructure, and skills to a new level of excellence.
The role requires a strategic thinker who can move the needle in areas such as Process Control, robotics, and intelligent automation to drive operational efficiency and innovation.
Key Responsibilities:
* Develop and execute a comprehensive automation strategy that aligns with the company’s overall business objectives and drives competitive advantage in the marketplace.
* Foster a culture of innovation and continuous improvement in automation practices, ensuring alignment with emerging technologies and industry trends.
* Champion the development and implementation of advanced Manufacturing Process Control Systems and other automation tools to streamline processes and enhance productivity, adaptability and agility.
* Establish standardized solutions and governance frameworks across all global sites to ensure consistency, efficiency, effectiveness and compliance across all nodes, in line with site and Supply Chain strategies
* Lead and oversee the implementation of the Assets Management Framework and maturity roadmaps for automation.
* Lead the transformation of automation skills and infrastructure, enhancing the organization’s ability to leverage advanced technologies, including AI, machine learning, and IoT, to optimize operations.
* Estab...
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Type: Permanent Location: Athens, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-19 08:26:30
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Data Analytics & Computational Sciences
Job Category:
Career Program
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson's Innovative Medicine - Research & Development (JRD) is seeking to recruit a Postdoctoral Scientist, for a fixed term of 2 years, specializing in Artificial Intelligence (AI) based solutions for Neuroimaging Data.
The most preferred location for this position is Cambridge, Massachusetts USA or Beerse, Belgium.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
The AI/Machine Learning and Digital Health team within Johnson & Johnson Innovative Medicine R&D designs cutting-edge insights and solutions employing various data sources across multiple disease areas.
We are in search of an exceptional postdoctoral scientist with key responsibilities:
* Design, develop, and implement cutting-edge AI and computer vision solutions to address high-priority scientific challenges in biomedical imaging.
Your work will directly contribute to advancements in drug discovery and healthcare.
* Develop and optimize state-of-the-art models to extract actionable insights from complex, unstructured biomedical image data.
* Contribute to the development of scalable core technologies that enable the deployment of advanced computer vision solutions across a variety of imaging modalities, including radiology, and brain imaging.
* Develop and deploy models using containerization technologies such as Docker and Kubernetes to ensure scalable and efficient deployment in production environments.
* Utilize high-performance computing resources and techniques to manage and process large-scale datasets and complex models efficiently.
* Clearly articulate complex technical methods and results to diverse audiences, including scientists, stakeholders, and decision-makers, to facilitate informed decision-making and drive project success.
* Author sci...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-19 08:26:26
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
FR001 Issy Les Moulineaux
Job Description:
Vous voulez contribuer à un projet de grande envergure et avoir un impact sur le monde qui vous entoure ?
Intégrer Janssen, la division pharmaceutique du groupe Johnson & Johnson, leader mondial dans le domaine de la santé (126 500 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.
Johnson & Johnson Innovatine Medicine France recrute un/e alternant/e pur 12 mois en Affaires medicale sur une gamme Neuroscience.
Localisation : Issy-les-Moulineaux
Date de démarrage : Septembre 2025
MISSIONS PRINCIPALES
Assister l’équipe Medical Education Neurosciences :
* Participer aux réunions d’équipe
* Elaborer des outils de communication en partenariat avec des agences de création : cartons d’invitation, campagnes de mail, vidéo...
* Être force de proposition dans l’élaboration des formats et des contenus scientifiques des évènements MedEd (symposium, standalone, webinaire, replay…)
* Participer à l’organisation des événements scientifiques et s’assurer du bon déroulement, de la satisfaction des intervenants et des participants
* Mise en œuvre et suivi opérationnel du plan Medical Education
* Assurer la coordination des événements avec l’équipe logistique évènementielle (PRP) ainsi qu’avec les équipes médicales et promotionnelles du terrain
* Elaborer et analyser des questionnaires de satisfaction pour améliorer les programmes
* Assurer la validation réglementaire des programmes MedEd et outils de communication
* Aider au suivi des contrats, récupération ACA, etc.
Assister l’équipe Medical Advisor Neurosciences :
* Participer aux réunions d'équipe
* Aider à la validation des documents marketing
* Aider à la création et mise à jour des diaporamas des différentes présentations effectuées par l’équipe
* Effectuer la veille et recherche bibliographique et animer des r...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-04-19 08:26:16
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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:
New Brighton, Minnesota, United States of America, Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Clinical Research Associate II - Shockwave Reducer (Remote) to join our team.
The position is FULLY REMOTE and can sit anywhere in the US.
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 Clinical Research Associate II (CRA II) is responsible for facilitating in-house set up, activation, maintenance and closure of Reducer device global clinical trials while gaining experience in clinical trial management processes.
The CRA II will work closely with Investigators, Site Personnel and Vendors to ensure compliance with protocol and overall clinical objectives.
In collaboration with the Clinical Research Manager, the CRA II maintains consistent CRF data quality and discrepancy interpretation across sites.
The CRA II will develop a basic understanding of the disease and indication.
Essential Job Functions
* May participate in study design and study set up activities
* May conduct site visits (pre-study, initiation, interim and close-out visits) to ensure protocol compliance, accurate and thorough data collection, and appropriate study conduct
...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-19 08:26:13
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
Budapest, Hungary
Job Description:
Manager Clinical Operations is accountable for the operational management and successful country execution of all phases of clinical trials within assigned therapeutic area(s) or specific role(s), including resource allocation, adherence to timelines and budget, compliance with relevant Standard Operating Procedures (SOPs), policies, Health Care Compliance (HCC) and local regulatory requirements.
The Manager Clinical Operations supports Country Head in shaping and managing local organizational structure to ensure its optimal efficiency and demonstrates effective issue management.
This individual is responsible for line management of Local Trial Managers (LTM), Site Managers (SM), Clinical Trial Assistants (CTA) and/or other staff, as required.
Oversees staff performance, development, training, project assignments, workload distribution and supports issue resolution with direct reports.
Ensures alignment of local goals with organizational objectives.
Drives innovative solutions and process improvements for the assigned therapeutic area(s), country, and R&D overall.
Principal Responsibilities:
* Provide line management to direct reports including setting goals and objectives, performance evaluation and talent development.
* Evaluate and forecast resource needs for assigned portfolio and/or other specific area of responsibility, as required and agreed with local management accordingly.
* Responsible for deployment of the One Delivery Model through collaboration and oversight of vendors.
* Accountable for the acquisition of new talents and development of human resources.
* Guide direct reports in issue resolution and communication with involved stakeholders.
* Lead organizational changes and effectively communicate on priority shifts as required.
* Review and approve expenses in compliance with the company policies.
* Demonstrate leadership behaviors in alignment with J&J Leadership Imperatives.
* Foster an environment that encourages sharing of ideas, information and best practices (internal and external to the organization).
* Provide coaching and mentorship as needed, including conduct of accompanied site visits as appropriate.
* Define, execute or support of long ter...
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Type: Permanent Location: Budapest, HU-BU
Salary / Rate: Not Specified
Posted: 2025-04-19 08:25:53
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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:
Quality
Job Sub Function:
Quality Training
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Trainer Opleiding & Ontwikkeling – Strategy & Support
De functie in het kort
Deze functie draagt sterk bij aan de ontwikkeling de juiste attitudes binnen een cultuur waarbij leren een aangeboren onderdeel is van wat we doen en hoe we ons gedragen en waar mensen gemotiveerd zijn om te leren, te groeien en te presteren.
De specialist opleiding & ontwikkeling zorgt er voor dat alle mensen op alle niveaus binnen de organisatie de nodige kennis en vaardigheden bezitten en of ontwikkelen om te kunnen voldoen aan de korte- en lange-termijnambities van de organisatie, rekening houdend dat de juiste attitudes ten opzichte van de trainingsdoelstellingen gehandhaafd worden.
De juisten doelstellingen worden opgesteld in functie van de stakeholders.
Deze worden bekomen door het uitvoeren van adequate trainingsbehoeften analyses.
Daarna staat de specialist garant voor het ontwikkelen, uitwerken, implementeren en evalueren van de verschillende leerinitiatieven.
Dit zal gaan om een contract van onbepaalde duur.
Wat verwachten we van jou?
Onder hoofdtaken verstaan we:
* Je werkt samen met interne stakeholders en teams om de leerbehoeften te identificeren (analyse van trainingsbehoeften) en om leeractiviteiten in te plannen.
* Je gaat leeractiviteiten en materialen ontwerpen die de overdracht van het leren naar de werkplek ondersteunen.
* Leeractiviteiten uitvoeren en evalueren.
* Voortdurende focus op het vergroten van het leervermogen van de doelgroep.
* Het weten wanneer en hoe trainingen aan te bieden en te integreren in dagelijkse activiteiten op de werkvloer.
* Het beoordelen van de leervoortgang van de toegewezen focusgroepen.
* Ondersteuning en coachen van stakeholders bij het opleiden van hun collega’s.
* Faciliteren van bijeenkomsten waar medewerkers kunnen ontdekken met hoe en met wie ze kunnen samenwerken om hun leerdoelstellingen te bereiken
* De organisatie adviseren over L&D.
* Je onderzoekt en rapporteert over nieuwe ontwikkelingen en inzichten in L&D die kunnen leiden tot betere organisatieprestaties.
* Je onderzoekt en experimenteert met nieuwe en innovatieve didactische leermethodes.
* Ontwerpen en implementeren van processen om de kennisproductiviteit te verbeteren en de kennisover...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-19 08:25:43
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
People Leader
All Job Posting Locations:
US026 PA Spring House - 1400 McKean Rd, US064 CA San Diego - 3210 Merryfield Row, US328 CA Santa Clara - 5490 Great America Pkwy, US337 MA Cambridge - 301 Binney St
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Associate Director, In Silico Discovery, Biologics to be in Spring House, PA; Cambridge, MA; or La Jolla, CA.
Purpose: We are seeking a creative and self-motivated Associated Director to join our In Silico Discovery Biologics team.
As we expand our AI/ML capabilities in antibody design and multifunctional optimization of complex biologics, we are looking for an experienced scientist to play a key role in applying the methods from this initiative to accelerate therapeutic discovery.
The ideal candidate will be a highly collaborative researcher who is passionate about the potential impact of these computational techniques on biologics design and development.
This is an exciting opportunity to join an enthusiastic, diverse, and global community of in silico scientists committed to bringing innovative new medicines to patients.
The Associate Director will collaborate with Biologics Discovery (BD) scientists to effectively apply AI/ML models to enhance the antibody discovery process.
This role involves leveraging advanced computational techniques and data analysis to accelerate the identification and optimization of antibody candidates.
By integrating AI/ML models with experimental data, the team will aim to predict candidate efficacy, facilitate design solutions and streamline the overall workflow from initial screening to lead optimization.
Additionally, fostering cross-disciplinary collaboration and continuous knowledge transfer between in silico approaches and laboratory efforts will be crucial for driving successful outcomes in antibody discovery and development.
You will be responsible for:
...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-19 08:24:47
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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:
Strategy & Corporate Development
Job Sub Function:
Digital Strategy & Deployment
Job Category:
People Leader
All Job Posting Locations:
Zug, Switzerland
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson is recruiting for a Global Lead of Automation, based in a J&J manufacturing site in Athens GA, Gurabo PR, Cork IR, Leiden NL, Beerse/Geel BE, Schaffhausen CH, or Latina IT. This position is required to be on site 3 days per week.
Position Summary:
The Global Lead of Automation is a critical leadership role responsible for transforming the organization’s automation capabilities, infrastructure, and skills to a new level of excellence.
The role requires a strategic thinker who can move the needle in areas such as Process Control, robotics, and intelligent automation to drive operational efficiency and innovation.
Key Responsibilities:
* Develop and execute a comprehensive automation strategy that aligns with the company’s overall business objectives and drives competitive advantage in the marketplace.
* Foster a culture of innovation and continuous improvement in automation practices, ensuring alignment with emerging technologies and industry trends.
* Champion the development and implementation of advanced Manufacturing Process Control Systems and other automation tools to streamline processes and enhance productivity, adaptability and agility.
* Establish standardized solutions and governance frameworks across all global sites to ensure consistency, efficiency, effectiveness and compliance across all nodes, in line with site and Supply Chain strategies
* Lead and oversee the implementation of the Assets Management Framework and maturity roadmaps for automation.
* Lead the transformation of automation skills and infrastructure, enhancing the organization’s ability to leverage advanced technologies, including AI, machine learning, and IoT, to optimize operations.
* Establish key performance indicators (KPIs) to measure the effectiveness of a...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-04-19 08:24:40
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Pharmaceutical Sales
Job Sub Function:
Sales – Rare Diseases (Commission)
Job Category:
Professional
All Job Posting Locations:
Portland, Maine, United States
Job Description:
Johnson & Johnson Innovative Medicine is searching for the best talent for a Rare Disease Account Manager (RAM) for Immunology Autoantibody Diseases to cover the Portland, ME Territory.
This position is field based.
About Immunology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine
The Rare Disease Account Manager will consistently achieve or exceed sales objectives within their Local Healthcare Market (LHM).
The Rare Disease Account Manager will report to a Senior District Sales Manager. The RAM owns the total market, developing and executing a strategy to identify patient opportunity, drive demand, and remove fulfillment barriers.
To achieve the business goals and meet customer needs, you will also ensure alignment with internal field partners, including Thought Leader Liaisons (TLLs), Area Business Specialists (ABSs), Field Reimbursement Managers (FRMs), Key Account Managers (KAMs) and Medical Science Liaisons (MSLs).
The RAM will be responsible for:
* Drive outstanding territory sales performance and product demand to ensure sales forecasts are met or exceeded within the LHM by building and sustaining strong, trusting relationships with customers and influencing key stakeholders
* Leverage company approved marketing resources to effectively demonstrate clinical value as a solution to address identified customer and patient needs.
Leverage payer acumen to educate on patient access and affordability options.
* Analyze qualitative and quantitative market data to assess business opportunities and priorities.
* Build LHM-specific business plan and account plans to drive growth.
* Be the quarterback of...
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Type: Permanent Location: Portland, US-ME
Salary / Rate: Not Specified
Posted: 2025-04-19 08:24:27
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ERM is seeking a Managing Consultant, Environmental, Health, & Safety Management Systems and Compliance to join our Sustainable Operations technical team in Houston or Austin, Texas.
In this role, you will manage and contribute technically to challenging environmental compliance, management systems, auditing, and compliance assurance projects and programs for clients locally, nationally, and internationally.
The successful candidate will also network with ERM's national management systems and compliance technical teams to share consulting opportunities, business relationships, and the application of best practices to address client needs.
This is an excellent career opportunity for a mid-level professional looking to advance their career with a global environmental leader, and to make a significant impact in successfully implementing ERM's global strategy.
RESPONSIBILITIES:
* Provide leadership and strategic direction for expanding ERM's management systems and compliance service area and client base. Identify and develop new opportunities, prepare effective technical proposals, and take active leadership role in developing new business with new and existing clients. Develop and expand client relationships that generate repeat business.
* Direct strategic management systems and compliance assurance programs for a variety of clients with complex technical/regulatory issues. Work closely with clients and develop strong relationships to understand specific processes and develop compliance strategy to help clients maintain maximum operating flexibility.
Achieve client’s expectations for scope, budget, schedule, and quality.
* Serve as a senior technical resource on management systems, compliance, and/or auditing programs.
* Capitalize on existing client relationships to expand ERM’s profile and market share in the regional and global management systems and compliance markets (through a combination of excellence in technical delivery and business development).
* Mentor junior and mid-level staff in the proper planning and execution of projects, and in directing or conducting independent technical reviews of deliverable work products.
* Support the general growth and development of ERM’s global services. Collaborate with other ERM global practitioners to execute projects, including participating on teams comprised of management systems and compliance professionals from multiple offices around the global organization.
REQUIREMENTS:
* BS/MS in engineering (chemical, mechanical, environmental), environmental science, or related degree.
Or equivalent experience.
* Experience or interest in supervising direct reports.
* 4+ years (7 years preferred) of relevant consulting experience with multimedia environmental compliance and management system.
* 4+ years (7 years preferred) of experience in managing projects, including scope, schedule and budgets, communications, and interactions with...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-19 08:24:05
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ERM is hiring an EHS Manager in Fremont, CA.
In this critical role, you will be responsible for supporting the facility and engineering teams for a pharmaceutical client.
The EHS Manager will be establishing, implementing, managing and continuously improving the safety programs for the facility.
The EHS Manager will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
The role includes strategic Safety planning as well as a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (40 hours/week), limited-term role for the duration of 6 months.
RESPONBILITIES:
* Prepare and submit local, State and other as required regulatory reports, ensuring site Safety Regulatory compliance
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends
* Provide timely, high quality Safety technical support/training.
Design, conduct and oversee Safety training
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
Develop and manage an internal audit program to assess compliance with legal and company requirements and identify opportunities for improvement
* Coordinate the completion of job safety analyses and risk assessments.
* Establishment of site Safety policies, objectives, key performance indicators and targets that reflect local needs and alignment with the Client’s long term Safety strategy.
Establish program to manage the site’s different Safety risks and impacts, coordinated within an overall Safety management system
* Review change proposals (including capital projects and new product introductions) to identify potential Safety issues and participate in their resolution
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Coordinate local business continuity, emergency response, and crisis management plans.
Develop and test the plans with realistic scenarios.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* 5 years minimum of relevant Health and Safety experience required.
* CSP or ASP or other safety certifications preferred.
* Previous Technology or Pharmaceuticals industry experience preferred.
* Experience with OSHA programs including hazardous materials, personnel protective equipment, fall protection, machine guarding, electrical safety, fire protection, hearing conservation program, respiratory protection program, and toxic and hazardous substances and with EPA's SPCC and RCRA programs.
* Experience with LOTO, Hot Work, Confined...
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Type: Permanent Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-19 08:23:23
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ERM is hiring a Construction Safety Specialist for a key technology client in the Los Angeles, CA metropolitan area (Culver City).
In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs for several ongoing construction projects.
The Construction Safety Specialist will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (40+ hours/week), fixed-term position for a duration of one year, renewable.
RESPONBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Act as Owner’s representative while interacting with contractors.
* Provide daily observations of on-site safety practices.
* Provide timely, high quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Review and evaluate Soil Management Plans and hazardous materials, and waste management compliance with regulatory agencies.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans.
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, preferably with commercial/office building construction or large projects.
CHST certification a plus.
* Bilingual Spanish a plus.
* Proficient with the management of high-risk activities including electrical safety, excavation, confined spaces, fall protection, material handling, rigging and crane operations.
* Experienced in communicating and problem solving as a team with sub-contractors is required.
* Experience with demolition preferred.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, c...
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Type: Contract Location: Los Angeles, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-19 08:23:21
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Your Job
We are looking for a passionate and experienced professional who is eager to contribute to groundbreaking advancements in papermaking technology and grow with Georgia-Pacific.
Experience in papermaking and innovation pipeline development will enable you to drive impactful projects and contribute to Georgia-Pacific's success.
Join Georgia-Pacific as an R&D Research Fellow at the Neenah Technical Center! You'll play a key role in our innovative papermaking technology development team, driving advancements that will shape the future of our industry!
What You Will Do
* Collaborating with cross-functional teams to drive innovation.
* Design, develop, prototype, and test cutting-edge papermaking components, equipment, and machinery.
* Create specifications for new parts or prototypes and identify the best materials and processes to ensure top-notch quality and performance.
* Develop strategies to guide organizational investment decisions through experimentation and landscape studies.
* Analyze and test prototypes to identify weaknesses and improve processes.
* Develop as a Subject Matter Expert in structured papermaking technology.
Get informed by using internal and external resources to proactively seek out best knowledge.
Establish and expand knowledge processes that build networks with our key partners, including Operations, Engineering, Product Development, and Preferred Suppliers to drive transformation within the company.
Participate in troubleshooting, training, and knowledge transfer to provide direction to team members.
* Identify and lead research projects involving papermaking technologies for our manufacturing processes of tissue-based consumer products, leading to new or improved products or machine performance.
Use economic thinking to determine viability, use the scientific method to evaluate, use statistical process control to analyze data, and use written and verbal techniques communicate and document the results and next steps to various groups, including business, leadership and operations in a timely and effective way.
* Translate business priorities into actionable development initiatives.
Identify and coordinate key resources to work as a team to execute project initiatives and experiments that pursue new technology and support business goals.
Proactively address and solve problems and analyze data with a creative and open-minded approach.
Support scale-up trials and troubleshooting within production facilities to eliminate waste, increase productivity, reduce cost, develop future grades and future assets.
* Support the organization through developing Intellectual Property strategies that include landscape investigation, invention disclosures, patent applications and maintaining trade secrets.
Improve current test methods or develop new test methods for characterizing and evaluating various papermaking technologies.
Be creative and think beyond the obvious.
* Utilize...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-19 08:21:14
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Quality Control Inspector
Location: Houston, Texas
Overview:
Bray International is seeking a skilled Quality Control Inspector to join our team in a fast-paced industrial manufacturing environment.
If you are passionate about ensuring product quality and have at least four years of experience in quality inspection, we encourage you to apply.
This is an exciting opportunity to contribute to a leading company in the industrial valve and actuator industry.
Key Responsibilities:
* Perform incoming inspections on purchased parts, subassemblies, and finished products to ensure compliance with engineering drawings and customer standards.
* Review Material Test Reports (MTR) and Certificates of Conformance (CofC) against relevant standards.
* Analyze Non-Conformance Reports (NCR) to identify trends and generate Corrective Action Reports (CAR) as needed.
* Create Non-Conformance Reports and other departmental reports as assigned.
* Evaluate issues and make initial recommendations for corrective actions to supervisors.
* Investigate failures to determine root causes and propose remedial actions.
Qualifications:
* Minimum of four years’ experience in quality control within the industrial manufacturing sector.
* Experience with Positive Material Identification (PMI) preferred.
* Proficient in computerized record-keeping and standard software applications.
* Strong written and verbal communication skills.
* Skilled in using and calibrating precision measuring equipment (e.g., micrometers, height gauges, calipers, dial indicators, bore gauges).
* Knowledge of ISO 9001:2008/2015 and API standards.
* Ability to analyze and determine the best inspection methods for product conformity.
* Proficient in interpreting engineering drawings and understanding Geometric Dimensioning and Tolerancing (GD&T).
* Experience with Coordinate Measuring Machines (CMM).
* Ability to manage multiple tasks in a fast-paced environment while meeting delivery requirements.
* High School Diploma or equivalent required.
Physical Demands:
* Must have 20/20 vision (correctable) without color blindness.
* Ability to lift up to 20 pounds.
Note: Immigration sponsorship is not offered for this position.
Why Work for Us?
At Bray International, we are a global leader in providing industrial valves, actuators, and related control products.
We are known for our innovative flow control solutions and are looking for individuals who share our commitment to excellence, integrity, and collaboration.
What We Offer:
* Career Growth: We offer numerous opportunities for advancement within the organization.
* Comprehensive Benefits: Enjoy benefits such as:
+ Life, medical, dental, and vision insurance
+ Paid holidays and vacation
+ 401(k) plan with matching contributions
* Healthy Work Environment: We provide a smoke-free, drug-free workplace to ensure a sa...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-19 08:20:49
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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!
Your Role: Global Innovation Strategy Lead – Pet Health Parasiticides & Infectious Diseases
The Global Innovation Strategy Lead – Pet Health Parasiticides & Infectious Diseases will play a critical role in defining and driving the innovation strategy of our Parasiticides and Vaccines businesses, including the refinement of innovation target areas and prioritization of pipeline assets for resource allocation.
He/she will be responsible for assessment of BD opportunities, pipeline asset forecasts at multiple milestones, as well as key inputs into the launch of global assets, including the development of global brand positioning statements, pricing recommendations and brand name selection.
Your Responsibilities:
* Lead strategic direction for assigned segments, with expertise in Elanco’s portfolio, market trends, competitive landscape, and future technologies to maximize global portfolio value.
* Oversee the commercial evaluation of Innovation Target Areas, Product Profiles, and Launch Labels, collaborating with regional marketing, R&D, and technical teams to align R&D priorities.
* Manage global brand development during launch preparations, including brand name, positioning, and pricing recommendations, while ensuring cross-functional execution.
* Develop business opportunities for pipeline entry and commercialization decisions, providing clear forecasts and scenarios to inform strategy and decisions.
* Establish governance mechanisms to ensure effective input from regional stakeholders and maintain strong cross-functional alignment across key processes and strategic initiatives.
What You Need to Succeed (minimum qualifications):
* Education: MBA preferred and/or bachelor's degree in marketing, business administration, or a related field.
* At least 10 years of experience in product marketing, brand management, project management, or product launch leadership roles.
* Minimum of 10 years of animal health experience with a detailed understanding of global dynamics in PH Prevention
* Proven understanding ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 193000
Posted: 2025-04-18 08:32:06
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SmartWorks is seeking a talented and motivated Technical Consultant who can balance their business knowledge, technical skills and strong interpersonal skills.
The Technical Consultant will interact with our customers, development teams and third-party software vendors to gather and document requirements, deploy applications and provide implementation support and training.
As a Technical Consultant, you will be required to travel throughout North America approximately 30% of the time when safe and appropriate.
While you're not traveling throughout Canada and the US, you will be able to work remotely from home or out of any of the Harris offices.
This role is available remotely within Canada and the US.
This role requires travel up to 30% in North America.
A valid passport is required.
What your new role will be:
* Design and implement SmartWorks solutions to meet customer requirements
* Integrate SmartWork’s application suite with 3rd party software interfaces
* Develop and maintain project documentation, standard operating procedures, and other documentation as required
* Lead or assist in training sessions with SmartWork’s customers and provide implementation support
* Act as a liaison between SmartWorks, customers, 3rd party vendors and industry consultants
* Provide consulting services based on knowledge of Smart Metering infrastructure and best practices on analysis of corresponding data
* Provide the Project Manager with regular updates on progress, issues and ideas for resolution, and successes
What we are looking for:
* Experience in the technical field (for example, Electric or Computer engineering, Computer Science) or a degree/diploma in the related field
* Strong grasp of SQL and one or more Enterprise Database Software such as SQL Server, Oracle etc
* Comfortable working in Linux and Windows
* Ability to travel in North America up to 30% of the time
* 5+ years of relevant work experience in software implementation
* Strong working knowledge of object-oriented design (C/C++ or Java)
* Previous experience in the Utilities industry
What will make you stand out:
* Possess strong analytical skills to understand requirements
* Demonstrate excellent verbal and written communication skills in English
* Can work independently, but most importantly, as a team player
* Demonstrate positive attitude and determination
* Previous experience in training customers and writing technical documents
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About us:
SmartWorks empowers utilities to navigate change and unleash the potential of the smart infrastructure.
At SmartWorks we are committed to delighting our cust...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 90000
Posted: 2025-04-18 08:31:23
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Your Job
enMotion®, Compact®, and SmartStock® are all market-leading brands of away from home GP PRO products by Georgia-Pacific.
Our dispensers for each of those brands are examples of the innovative devices we develop, manufacture, and market.
If you're excited by an opportunity to continuously learn and grow while supporting those brands, we'd like to talk with you.
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.
We are seeking a Test Engineer to help us maintain our market leadership in our devices test lab at our Technical Center in Neenah, Wisconsin.
As a test engineer, you will have a great opportunity to shape the operation of our lab in an environment that fosters innovation and creativity and rewards you for value created.
Our Team
The Georgia-Pacific devices test lab team represents the people who use our dispensers and products every day and the maintainers who service them.
We are entrepreneurs who innovate daily and collaborate cross-functionally to design, develop, test, and manufacture products and execute projects that create value for our consumers, customers, communities, and company.
We value lifelong learners who want to contribute and grow with us.
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
Device Testing: Lead the planning, development, and execution of GP PRO device and product validation plans in support of our product development process.
Testing Efficiency: Lead the investigation, development, and implementation of custom test equipment, test fixtures, test methods, and instrumentation to streamline device testing through automation and data acquisition.
Test Protocols: Lead the investigation, development, and implementation of custom test protocols in support of validation and verification testing.
Designed-In Reliability: Actively participate in FMEA reviews to build device performance, reliability, and durability into the design of each device.
Test Status: Maintain and proactively share the status of device and product testing in the lab and the test queue.
Continuous Improvement: Implement continuous improvement processes to continually increase lab efficiency.
Test Lab Capabilities: Periodically and proactively recommend changes to test lab technical capabilities as device development needs shift.
Identify validation failures, file observations, and troubleshoot mechanical failures.
Work with cross functional team members to support root-cause analy sis.
Who You Are (Basic Qualifications)
* Bachelor's degree in engineering or science or equivalent experience
* At least five years of experience in product testing
* Familiarity with test automation tools and scrip...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-18 08:28:53
