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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 Technician
The position will include routine testing of in process antigens and final product samples for the release of veterinary vaccines. The individual will be responsible for ensuring all methods are performed as written and filed with regulatory agencies and standard operating procedures.
Your Responsibilities:
* Perform required tests for bulk antigens, final products, and raw materials, as well as other procedures necessary to support company and laboratory objectives to meet specified timelines.
* Maintain aseptic laboratory technique at all times and ensure accuracy of test results through precision and attention to detail.
* Maintain accurate and concurrent testing records and ensure compliance with Company SOPs and specifications, USDA, and cGMP regulations. Assist with updating, writing, and maintaining SOP’s, bench records and data entry for the department.
* Environmental monitoring of clean rooms and personnel: assisting in and/or performing microbial and particulate tests (air sampling).
* Provide effective training as requested, confirming that individuals are trained on the procedure at hand and all required training documentation has been completed.
What you need to succeed (minimum qualifications):
* High School Diploma or equivalent required.
* Experience in working in a team environment and handling multiple tasks simultaneously.
* Proficient in Microsoft Word and Excel, capable of using a controlled informatics system.
What will give you the competitive edge (additional preferences):
* Bachelor of Science degree in Microbiology, Virology, Bacteriology, Biology, or related field
* Minimum of four (4) years of laboratory experience.
* Fundamental experience in cell culture, viral and/or bacterial propagation.
* Experience in biotechnology and aseptic technique.
Other Information:
* Location: Winslow, ME (Onsite)
* Shift: Monday-Friday, 7am-3:30pm (evening, weekend, and holiday hours may be required)
* Must b...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: 27.12
Posted: 2025-04-22 08:35:47
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En tant que gestionnaire de produits, ce professionnel sera chargé de guider la découverte et le développement de solutions innovantes qui répondent aux besoins futurs du marché.
Il collaborera avec les ingénieurs, les chercheurs et les dirigeants pour définir la vision du produit, hiérarchiser les initiatives et piloter le développement du produit.
Responsabilités et tâches:
* Définir et gérer la feuille de route des produits de R&D, en veillant à l'alignement sur les objectifs et les stratégies à long terme de l'entreprise.
* Diriger la découverte et l'exploration des technologies et tendances émergentes afin d'identifier de nouvelles opportunités de produits.
* Collaborer avec les parties prenantes au sein de l'organisation.
Exigences:
* Baccalauréat en informatique, en ingénierie, en gestion de produits ou dans un domaine connexe, ou expérience pertinente.
* Plus de 4 ans d'expérience dans la gestion de produits, avec un accent sur les produits logiciels.
* Expérience technique et compréhension des processus de développement de logiciels.
* Expérience de la gestion du cycle de vie des produits, de la conception au lancement.
* 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.
Un atout à ne pas négliger:
* Expérience de l'application des règles de stationnement, des paiements mobiles, des tribunaux et des recouvrements :
* Expérience des logiciels de stationnement, de circulation, d'application des règlements et des codes
* Expérience de l'application des règlements de stationnement, des paiements mobiles, des tribunaux, du recouvrement
* Expérience de la reconnaissance automatisée des plaques d'immatriculation (ALPR/ANPR).
*Seuls les candidats retenus seront contactés.
Harris est un employeur souscrivant au principe de l'égalité des chances et les membres des groupes cibles suivants sont encouragés à postuler : femmes, personnes handicapées, autochtones et minorités visibles.
Si vous êtes une personne handicapée, une assistance au processus de sélection est disponible sur demande.
L'équipe de Harris Talent Acquisition n'utilise pas de SMS pour contacter les candidats ou solliciter des informations confidentielles.
Nous encourageons tous les candidats à postuler aux postes annoncés.
Ils seront contactés soit par un responsable de Harris, soit par un membre de l'équipe d'acquisition de talents pour un entretien, une fois que les critères requis auront été remplis.
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As a Product Manager, this professional will be responsible for guiding the discovery an...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-04-22 08:35:27
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
Job Description:
About Oncology
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 Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
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 MSL to be in Shefayim.
Key Job Activities:
* Keeping abreast of medical and scientific knowledge
* Creating and fostering a network of partnerships with experts
* Working cross-functionally within the company to become a valuable team member
* Providing high level scientific engagement with experts, while utilizing multichannel platforms
* Initiator and coordinator of medical education activities and advisory boards, in alignment with Medical Manager
* Scientific support and training to company sales representatives and other peers
* Supports and initiates evidence generation via research and publications
* Gains valuable scientific insights contributing to the short & long-term strategic plans of the therapeutic area
* Skillful in implementing innovative solutions and ideas for multichannel engagement and data-collection
* Champions medical benefits of products and contributes to the fostering of innovative therapeutic approaches for patient's benefits
* Actively involved in strategy and action plans related to local reimbursement of products
The role is mainly field-based ( 85%) , requires agility with regards to travel & work hours
Requirements:
Education
MD, D.M.D, D.V.M, Ph.D.
(Pharmacy or Science)
Experience:
With preference for:
* Previous experience working in the pharmaceutical industry or research company- an advantage
* High-competency in project & customer-affairs management
Knowledge:
* Deep scientific & clinical kn...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-04-22 08:14:54
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
Job Description:
Job Description:
Janssen Sciences UC Ireland is recruiting for a QC Analyst - located in Ringaskiddy
Job Description
Performs advanced tests and analyses to assure that products align with established specifications.
Carries out complex calculations and documents test results.
This is a volume driven position that that directly touches product.
Compiles and analyzes data on reoccurring product defects to determine root cause.
Documents analysis results.
Analyzes raw material inspection logs for consistent failures.
Notifies purchasing and quality departments about suppliers that have provided inferior products.
Studies work processes, measurements and performance metrics to identify improvement areas.
Recommends new or modified procedures based on findings.
Collaborates with customers, suppliers and associates to define and improve quality standards and expectations.
Participates on process improvement teams.
Monitors and scrutinizes internal and external complaints and compiles data to be used in reports.
Performs analyses in order to achieve compliance with specifications using a wide variety of chemical, biological and physical standard procedures
Key Responsibilities:
* Attending daily meetings, working on own initiative.
* Testing and reviewing daily
* Training new analysts
* Always aim to meet site metrics
* Promoting 6S within the laboratories
Qualifications
Education:
A minimum of a bachelor’s degree in a science related discipline and 3 years of experience in a pharma company.
Experience and Skills:
* Experience in lab-based testing
* Proficient in Lab report writing.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
#RPOAMS
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:34
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Specialty Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States, Columbus, Ohio, United States, Detroit, Michigan, United States, Pittsburgh, Pennsylvania, United States of America
Job Description:
This is a field-based role available in multiple states within the US.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from various locations to apply and encourage you to review the following states/cities where this opportunity is available:
Cleveland, OH
Columbus, OH
Pittsburg, PA
Michigan
Johnson & Johnson is recruiting for a District Business Manager to support our J&J Vision business, responsible for key distributor and direct accounts. The district for this position will include Cleveland OH, part of Columbus OH, Pittsburgh PA and Michigan.
This is a field-based position with the ideal candidate residing in Cleveland, OH.
About Johnson & Johnson
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/.
About Vision
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/medte...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:07
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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:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal Scientist, Analytical Comparability & Product Characterization – Advanced Therapies to be in Malvern, PA.
Purpose:
The Biotherapeutics Development - Analytical Development (BioTD - AD) group is seeking an upbeat, highly motivated Principal Scientist to focus on analytical comparability and product characterization for advanced therapy modalities. The individual would work with team to develop product comparability study approaches for advanced therapy modalities that will be endorsed by the health authorities. A successful candidate will have experience with the design, execution and optimization of a broad range of characterization assays and will have the opportunity to engage in multi-functional teams.
They will learn from and contribute to industry-leading drug discovery/development programs that has brought numerous quality therapeutics to patients and has made significant contributions to human health.
Primary Responsibilities:
·Design and lead the execution of analytical comparability studies for advanced therapy modalities across various stages of development.
·Lead the execution of the advanced methodologies associated with comparability and deep characterization of cell and gene therapy.
·Author or coordinate appropriate IND/IMPD/BLA/MAA sections & interact with regulatory agencies to address CMC-comparability and product characterization related inquiries.
·Optimally communicate comparability study plans, statistical justifications, and results and scientific data to cross-functional teams, project teams, and health authority as needed.
·Collaborate to develop innovative approaches to challenging solutions for analytical comparability strategy and product characterizati...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-21 07:58:03
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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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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
-
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:
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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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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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
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Credit Analyst II - 12 Months Contract - (Global Business Services)
Job Description
Credit Analyst II - (Global Business Services)
Your Job
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.
Role Overview & Primary Accountabilities:
* Responsible for review AR Aging and active following up outstanding debts from customers and meeting collection ADSO targets and maintain positive cash flow.
* Analyses customer ledgers and reconciles wit sales specialists and/or customers to ensure hanging balances are resolved, customer records are updated, customer issues and disputes are addressed on timely manner.
* Reviewing credit risk for new application / new customers by carry out credit worthiness checks and make credit limit recommendations, evaluate and mitigate credit risks.
* Conduct periodic credit evaluation and meeting with Sales team on existing customers, formulate and implement credit control procedures that is aligned with the company credit administration policy & procedure.
* Release held orders of customers and follows-up customers regarding adherence to collection / payment terms to avoid holding orders.
* Monitor past due and delinquent accounts and constantly follow up with Sales team and customers on collection activities and action taken.
* Issue monthly Credit / AR performance report for management's review.
* Prepare Inter-co billings and follow up payments.
* To attend to Auditors on audit schedules and AR enquiries.
* Proactively work and collaborate with internal customers to ensure the type and quality of services provided, support them in achievement of their business objectives, and efficiently provide the essential administrative support services to the organization.
* Provide training/briefing for new Sales personnel on the Credit policy & procedure, risk and reporting.
* Book monthly AR doubtful debts provision, early payment discount journals for month-end close.
* Other Ad hoc reports and request from management.
Continuous Improvement and Value Creation: -
* Support the development of a culture of continuous improvement by supporting LEAN concepts, tools, and methodologies to eliminate waste in all its form.
* Work collaboratively with other team members to identify opportunities to streamline and improve department efficiency and participate in the implementation of those opportunities.
* Value Creation mindset by identifying opportunities for innovation, optimizing processes to enhance effici...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-04-18 08:28:52
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Accounting Analyst II - RTR Operations (Global Business Services)
Job Description
Accounting Analyst II - RTR Operations (Global Business Services)
Your Job
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.
Role Overview & Primary Accountabilities:
* Maintain assigned SAP systems by ensuring that all relevant RTR Finance master data changes for SAP security, system tables, chart of accounts, internal orders, cost centers and profit centers are appropriate, authorized and documented.
* Ensure Finance security roles are in compliance with global segregation of duties matrix.
* Provide a source of system expertise, business knowledge and problem-solving capabilities to ensure sound analysis, recommendations and action programs in the maintenance and development of RTR module
* Perform period end closing for CO-PA (customer and product profitability analysis) for management reporting purposes.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 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 of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.
To succeed in this role, you will need the following qualifications:
Qualifications/Education/Experience R...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-04-18 08:28:46
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Accounts Payable Subject Matter Expert - (Global Business Services)
Job Description
Accounts Payable SME - (Global Business Services)
Your Job
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.
Role Overview & Primary Accountabilities:
Data Entry
* Managing and processing customer orders that are received via EDI, fax, or email.
* Demonstrating expertise in data entry by keying in all customer orders accurately within 24 hours of receiving or within appropriate cut off periods.
* Coordinate with 3rd party logistic team in warehouse/Distribution Center to ensure timely fulfillment of orders processed.
* Analyze business scenario and work closely with Process Manager to determine on correct solution, ensure the solutions meets business needs and carried out in accordance to global compliance standards
* Working closely with AP Team Leader to understand and gather operation requirements.
* Provide preliminary assessment on system capabilities against business requirements with the support and consultation from P2P RPA consultant.
* Perform UAT on the business solutions, implementation, monitoring and provision of post implementation support
* Participate in Global / Regional AP projects impacting the P2P operations, including requirements gathering, UAT, implementation and post implementation support.
* Provide ongoing support and expertise in day to day AP operations, including some trouble shooting and issues resolutions.
* Keep up to date and maintain high quality of training documentation, supporting respective AP Team Leader to update the relevant SOP on timely manner.
* Deliver solid knowledge training, updates and briefings to team to ensure full understanding of process and procedures after each project / enhancement carried out.
* Timely update the project status to manager and highlights any key impact to the operations
* Attend regular team meetings ( with respective AP Team Lead) to understand the concerns and operational issues from respective team and provide suggestions to improve or close the gaps to achieve overall KPI targets.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team comm...
....Read more...
Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-04-18 08:28:43
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Roche in 50 Worten
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein. Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Was macht unseren Bereich aus
Diagnostics Operations Penzberg ist Teil des globalen Produktionsnetzwerks der Diagnostics Division von Roche und als solcher der wichtigste Produzent von qualitativ hochwertigen Einsatzstoffen für diagnostische Tests.
Wir produzieren monoklonale Antikörper, Antigene, Enzyme und Nukleinsäuren aus Säugerzellkulturen und Mikroorganismen in einem Fermentationsmaßstab von 0,1 – 2.000 L.
Die daraus aufgereinigten Produkte werden in vielfältigen diagnostischen Tests, z. B.
für den Nachweis von Infektionskrankheiten eingesetzt.
Dein Team
Wir sind als Team besonders stolz auf die gute Mischung aus langjährig erfahrenen und jungen Mitarbeitern, die gerade ihre Ausbildung abgeschlossen haben.
Als Upstream-Produktionsbetrieb arbeiten wir mit einer großen Vielfalt an tierischen Zellen, Mikroorganismen und Viren der Risikogruppen 1 und 2 in mehreren Produktionsstätten.
Was dich erwartet
* Du fermentierst tierische Zellen oder Mikroorganismen im Maßstab 0,1 – 2.000 L
* Du kultivierst adhärente Zellen zur Produktion von Viren bzw.
viraler Komponenten
* Du führst die prozessbegleitende Analytik mit verschiedenen enzymatischen und molekularbiologischen Methoden durch und dokumentierst gewissenhaft
* Du führst erste Aufreinigungsschritte der Zielproteine und Nukleinsäuren durch
* Du beteiligst dich an der Durchführung von Desinfektions- und Hygienemaßnahmen
* Die Auswertung von Fermentationsansätzen und Mitarbeit bei der Erstellung von Herstellvorschriften zählt ebenfalls zu deinen Aufgaben
* Bei unserer technologischen Vielfalt wird dir nie langweilig – Fermentation in Edelstahl oder Single Use, Dialyse- oder Fed-Batch-Prozess, Cross-Flow-Filtration oder diverse Zentrifugationstechniken
* Darüber hinaus kannst du bei der Verbesserung unseres Technologie-Standards im Produktionsbetrieb mitwirken
Wir freuen uns auf dich mit folgender Qualifikation
* Du bringst eine erfolgreich abgeschlossene Ausbildung als Biologielaborant, Chemielaborant, Chemikant, BTA, CTA (m/w/d) oder einen vergleichbaren Abschluss mit
* Du hast Kenntnisse im Umgang mit Säugerzellen oder...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-04-18 08:16:14
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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 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.
* Relevant consulting experience with multimedia environmental compliance and management systems.
* 4+ years (7 years preferred) of experience.
* Experience in managing projects, including scope, schedule and budgets, communications, and interactions with clients.
5 years minim...
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Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-18 08:09:46
