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Your Job
Join Molex, a dynamic, fast-growing global leader in the tech industry, and make an immediate impact as an Internal Communications Business Partner.
Reporting directly to the Director of Corporate Communications, you will be at the heart of our employee engagement efforts, crafting compelling stories and content that connect every Molex employee to our Vision, business priorities, and vibrant culture.
In this role, you'll be the trusted communications advisor and storyteller for the entire organization, working closely with leaders and executives across departments.
You'll partner with business leaders on critical projects, helping them communicate with clarity, empathy, and purpose to keep employees informed, motivated, and aligned.
Your work will span a variety of internal communication channels, from crafting thoughtful emails and newsletters to collaborating with our in-house multimedia video team to bring stories to life.
You'll leverage your creativity and initiative to experiment with new ideas and approaches, ensuring our messaging is fresh, engaging, and impactful.
If you're ready to be a vital connector who shapes how our employees experience and understand the business, this role is for you!
Location: This is an onsite role based at our office in Lisle, IL.
What You Will Do
* Create clear, concise, and engaging messaging tailored for diverse audiences across multiple channels, including intranet posts, leadership emails, presentations, and video scripts
* Build and maintain strong, trusted relationships with key business leaders and stakeholders (ranging from department heads to executives) to provide strategic communication counsel and support
* Develop and execute comprehensive communication plans for organizational changes, initiatives, and business-critical projects that keep employees informed, aligned, and engaged
* Collaborate closely with the in-house multimedia video team to craft compelling video content that brings employee stories, profiles, and company initiatives to life
* Serve as a true communications business partner by proactively identifying opportunities to strengthen internal communications and foster two-way dialogue across the organization
* Experiment with innovative communication approaches and formats to continuously improve employee engagement and message effectiveness
* Manage and distribute internal content using platforms like SharePoint, ensuring accessibility and consistency of communications across the enterprise
* Support and contribute to internal events and campaigns, enhancing employee participation and reinforcing company culture
* Monitor and measure the impact of communication initiatives and adjust strategies based on feedback and business needs
Who You Are (Basic Qualifications)
* Experience in corporate or employee communications, journalism, or public relations
* Strong writing, editing, and storytelling skills to convey...
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Type: Permanent Location: Lisle, US-IL
Salary / Rate: Not Specified
Posted: 2025-09-13 10:01:09
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Procurement Specialist - Maintenance, Repair, and Operations
Job Description
Job Description
You are not the person who will settle for just any role.
Neither are we.
Because we are 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 will bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you will help us deliver better care for billions of people around the world.
It starts with YOU.
Kimberly-Clark is looking for an ambitious, self-driven and talented individual to join our NA Procurement team.
You will make a difference by managing strategic sourcing activities within the Indirect space.
You will develop category strategies and lead local execution activities.
You will support North America businesses to achieve business financial goals, including working capital and cost savings.
This role has responsibilities for K-C’s purchases of Build to Draw and OEM purchases on the MRO team.
You will build category expertise and provide guidance to regional teams in the context of stakeholder needs, data quality, and benchmarking/analysis.
You will lead Supplier Relationship Management by building and facilitating partnerships with strategic suppliers and key stakeholders.
In addition, you will establish strong relationships by providing indirect goods and services expertise and actively engaging stakeholders in procurement processes.
In this role you will:
* Manage the Build to Draw and OEM categories on the MRO team.
* Deliver regional procurement targets for categories in scope.
* Coordinate with regional business stakeholders on category needs and strategy (e.g., collect business requirements)
* Execute the category’s strategic initiatives.
* Create and maintain category management knowledge and processes to ensure the category strategies are informed, relevant and up to date.
* Manage region-specific supplier relationships, escalate, and resolve supplier continuity issues, etc.
* Monitor supplier performance indicators and initiate supplier reviews as required or in accordance with agreed programs to drive improvement and reduce risk across the regional enterprise.
* Build trust and credibility with suppliers by demonstrating integrity, commitment, and results orientation to drive and deliver results.
* Maintain an effective business relationship with all suppliers and stakeholders based on clear, concise communication.
* Lead bidding processes, negotiating pricing/terms and conditions, and final contract award and implementation.
* Identify hurdles and barriers to change, resolve where possible or escalate as appropriate.
* Ensure compliance to K-C Policies and internal controls.
The successful candidate will join the NA Procurement team and report to the NA Leader of MRO Procurement.
About You...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-13 08:42:25
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
Na Alcoa, você é uma parte essencial do nosso propósito: transformar potencial em progresso real.
Esta é uma oportunidade para você trazer sua riqueza de experiência para a equipe e ajudar a moldar o futuro da sustentabilidade com inovações que mudam o mundo e tecnologias de baixo carbono.
Você tem o poder de moldar as coisas para torná-las melhores.
Sobre a Oportunidade:
A Alcoa está buscando por Técnica(o) Projetista Especializada(o) para integrar nosso time na unidade Alumar na área da Refinaria em São Luís do Maranhão sendo o responsável por:
* Elaboração de Projetos: Criação e desenvolvimento de projetos técnicos e soluções de engenharia, utilizando softwares como AutoCAD em áreas da Refinaria, atuando principalmente em protocolos associados ao departamento
de integridade de ativos;
* Desenvolvimento de Modelos 3D: Criação de modelos tridimensionais de peças, produtos ou estruturas, facilitando a visualização e análise do projeto, atendendo as disciplinas de mecânica, elétrica e civil;
* Revisão e Atualização de Desenhos: Análise e modificação de desenhos técnicos existentes, garantindo a precisão e funcionalidade do projeto;
* Colaboração Multidisciplinar: Trabalho em conjunto com engenheiros, técnicos especializados, supervisores e executantes de atividades;
* Análise de Viabilidade: Avaliação da viabilidade técnica de projetos, considerando requisitos, especificações e recursos necessários;
* Suporte para elaboração de memoriais e análises estruturais: Trabalho em parceria com time de engenharia para elaboração de memoriais e análises estruturais.
O que você pode oferecer para a função:
* Técnico em mecânica, Eletroeletrônica, Eletrônica e Mecatrônica;
* Experiencia ampla com projetos de estruturas metálicas, peças mecânicas, tubulações, avaliações estruturais, máquinas de grande porte e integridade de ativos, sistemas de combate a incêndio, pontes rolantes com preferencial, atuações em área de refinaria;
* Conhecimento básica de projetos de Elétrica e Civil;
* Pacote Office Intermediário;
* Mandatório conhecimento e experiencia ampla em AutoCad e outros softwares de projetos e desenhos
O que está sendo oferecido:
* Líder global em sustentabilidade e excelência operacional
* Pacotes competitivos de remuneração e benefícios
* Construção de uma carreira de longo prazo em nossas operações locais e globais.
* Como uma empresa baseada em valores, agimos com integridade, operamos com excelência, cuidamos das pessoas e lideramos com coragem
* Reconhecida como uma das melhores empresas para se trabalhar pelo programa Great Place to Work
* Reconhecida...
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Type: Permanent Location: Sao Luis, BR-MA
Salary / Rate: Not Specified
Posted: 2025-09-12 08:29:39
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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/Medical Operations
Job Category:
Professional
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Massachusetts (Any City), New Jersey (Any City), New York, New York, United States, Pennsylvania (Any City), Texas (Any City)
Job Description:
Johnson & Johnson is recruiting for a Sr.
Technical Writer to join our MedTech Surgery business.
A pre-identified candidate for consideration has been identified.
However, all applications will be considered.
This is a remote role available in multiple [states/cities].
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.
About Surgery
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world.
Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer.
Patients are waiting!
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
The Sr.
Technical Writer provides oversight and execution of Clinical Evaluation Reports/Plans (CER) and Summary of Safety and Clinical Performance Reports (SSCP) for Ethicon Endo-Surgery within J&J Global R&D Medical Device sector.
DUTIES & RESPONSIBILITIES
Under supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position will be responsible for:
* Planning and writing CEPs, CERs (including State of the Art protocols and reviews) and SSCPs
* Mentoring junior writers.
* Conducting technical reviews to ensure document accuracy and compliance to local procedures, J&J guidelines and regulatory requirements.
* Partnering with cross-functional team members to address needs of each contributor.
* Leading daily activities to ensure timelines are met.
* Participating in works...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:42
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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:
Business Enablement/Support
All Job Posting Locations:
Bridgewater, Massachusetts, United States of America
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for a QC Technician III, Lyra.
Purpose: This role is responsible for conducting technical quality assurance inspections of incoming materials, parts, and components against established standards and specifications before they are accepted into inventory.
Inspection methods may include but are not limited to measurement of parts, visual inspection, and documentation review.
The candidate will also be responsible for ensuring the accuracy and completeness of records related to the production and testing of medical devices, ensuring compliance with regulatory requirements and company procedures.
This includes reviewing documentation, verifying data, and collaborating with other departments to resolve any discrepancies.
Qualifications:
* Perform routine product inspections and analyses, generally of finished goods, components, incoming materials, materials prior to be sent to external service suppliers, or new products, by observing, measuring, and recording data.
* Utilization of blueprint reading skills daily.
* Has general awareness of GD&T principles.
* Compares inspection results to defined requirements or specifications and documents differences found.
Compiles and inputs data into router, logbook and/or computer databases and documents findings.
* Completes record of inspection results, acceptance, rejection, and disposition.
* Consults with more experienced personnel to confirm presence of non-conformances and subsequent product disposition.
* Executes assigned NR actions within the applicable software application.
* Compiles data to identify trends, prepares reports on findings, and proposes corrective actions.
* Recommends and implements revisions, corrections and changes to test equipment, procedures, and methods.
* Perform document change management as per local procedures.
* Initiates and coordinates discussions with quality, engi...
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Type: Permanent Location: Bridgewater, US-MA
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:14
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Are you a current Elekta employee?
Please click here to apply through our internal career site Find Jobs - Elekta.
Want to join a team with a mission to improve and save lives?
We continually look for motivated and skilled individuals who are interested in supporting our customers – healthcare professionals who use our products to help patients and their communities.
We currently have the following opportunity available - please contact us for more details!
We don’t just build technology.
We build hope for everyone dealing with cancer.
The Technical Writer has proven experience identifying content requirements to develop high-quality and technically accurate customer facing and internal use content in an Agile based workflow.
This role independently manages projects and priorities in a deadline-driven environment and requires collaboration with cross-functional areas of Elekta’s global business, and in particular, with engineering.
This position warrants the highest level of professional representation from our department to the various product/scrum teams for which you will provide documentation support.
This role also requires support of projects, programs, and policies established by Elekta.
Responsibilities
* Develop and publish content using DITA XML.
* Deliver contextually relevant content, for a variety of clinical site personnel, using help topics, release notes, configuration guides, and other supplemental material.
* Develop software installation and upgrade procedure content (SIPs, UPGs).
* Collaborate with various product teams to ensure quality and accuracy of content.
* Take ownership of deliverables in your product area, identify documentation needs and areas of improvement.
* Regularly report your work status, obstacles, initiatives to the team lead.
* Identify risks and manage and/or escalate to the project team and functional management.
* Demonstrate ability to prioritize tasks and work simultaneously on multiple projects.
* Scope, resource, plan, track, and execute against release timelines, in close collaboration with other stakeholders.
* Actively contribute to continuous improvement initiatives within the Information Development department.
* Other duties as required.
This list is not meant to be a comprehensive list of all responsibilities assigned to this position.
What you bring
* BA or BS degree and/or certification in the field of Technical Writing is preferred.
* Working knowledge of software development, development pipelines, backend server concepts
* Current experience with DITA based documentation preparation tools.
* Current experience with Office tools, PowerPoint, Excel, Word.
* 5 years of experience managing, creating, editing, and reviewing technical documentation.
* Experience working in a Content Management System (CMS).
* Current understanding of Agile workflow; prior work in a Scrum envi...
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Type: Contract Location: San Jose, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:26:09
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We are currently hiring for a Part-Time Activities Assistant.
This position will plan, develop and direct the overall operation of the activities department in accordance with regulatory guidelines and our established policies and procedures and assure that an on-going program of activities is designed to meet the level of interests and abilities of each resident.
The availability to work weekend shifts is required.
This position will be working in the Health Center, Assisted Living, and Memory Care buildings.
ACTIVITIES ASSISTANT ESSENTIAL JOB FUNCTIONS:
Comply with all applicable rules, policies, standards and guidelines related to employment with
Westminster and its communities.
1.
Implement and conduct programs as assigned by the Activities Director, encouraging residents to attend.
Includes setup prior to and clean-up after completion of activities.
2.
Leads and assists residents groups on community outings.
3.
Conducts one-on-one activities with those residents requiring them.
4.
Completes documentation such as Assessments and Daily Attendance Sheets.
5.
Purchase and organize decorations and supplies for daily activities & holidays.
6.
Assist with decorating Health Center common areas.
ACTIVITIES ASSISTANT ESSENTIAL QUALIFICATIONS:
Education:
Possess a minimum of a high school diploma, with interests in recreation, crafts and music helpful.
Must have basic knowledge of food preparation and handling. Certified Nurse Assistant certificate preferred.
Experience and Basic Knowledge:
Must have experience in recreational and activities programs in senior citizens group nursing homes or related activities within the last two years.
Must be familiar with dementia or willing to learn about the condition.
To learn more about our culture and what it is like to work at Westminster Communities of Florida, follow us on our social channels (Facebook and Instagram) at @WestminsterCareers.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2025-09-11 08:21:33
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Deliver
Job Sub Function:
Warehouse & Distribution
Job Category:
Business Enablement/Support
All Job Posting Locations:
Ciudad Juarez, Chihuahua, Mexico
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
We are searching for the best talent for PRINCIPAL CUSTOMS TECHNICIAN
Purpose: To perform a variety of administrative duties related to the temporary import of materials and the export of finished products.
You will be responsible for:
Under limited supervision, and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Processes Import/Export documents in compliance with Mexican and US Customs requirements.
* Coordinates local traffic.
* Prepares Customs reports as required.
* Files all customs related documents.
* Comply and adhere to Internal Customs Department Procedures.
* Participate and promote activities to improve internal controls and requirements related to international business operations of the Company.
* Follow all company safety policies and other safety precautions within the work area.
Ensures compliance with Environmental Management System (EMS) responsibilities.
Is his/her responsibility to comply with Company policies and procedures as well as local, state and federal regulations of the countries related to customs activity.
* Follow J&J and EES Records Management Policies for Convenience Information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and third-party vendor if applicable.
* Follow J&J and EES Records Management Policies for Convenience Information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and third-party vendor if applicable.3
* Responsible for communicating business related issues or opportunities to the next man...
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Type: Permanent Location: Ciudad Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:45
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson is currently seeking a Quality Control Analyst for in the weekend shift to join our CAR-T Hub located in Beerse.
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/.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories will be operated from the existing Janssen Beerse site.
The QC Biotech analyst, CAR-T Europe is responsible for preparing and conducting testing of the different samples taken during the production process.
You are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
You will be responsible for:
* Perform analytical testing in compliance with all applicable specifications, procedures, GMP
* regulations
* Maintain a safe work enviroment in compliance with all applicable environmental, health and
* safety regulations
* Perform peer review of laboratory data
* Author and update SOPs, Wis and Protocols to support daily operations of the lab using the
* document management system
* Support laboratory related invetigation records and CAPAs
* Assist in the execution of internal audits
* Provide input to functional laboratory meetings
* Provide input and tak actions as a QC representative at cross-laboratory meetings
SHE responsibilities:
* Always strictly apply all applicable prevention rules and procedures
* Make correct u...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:37
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Sales Enablement
Job Sub Function:
Customer Success Management
Job Category:
Business Enablement/Support
All Job Posting Locations:
Chuo-ku, Tokyo, Japan
Job Description:
Position Overview
The Customer Service Specialist will ensure consistency for indirect Customer Service processes and procedures around areas such as clinical study device shipment, new sales hires, Salesforce case monitoring, continual improvement projects, order system error handling, and reporting to support the success of the field sales force.
The Customer Success Specialist handles many complex inbound and outbound inquiries related to the success of our business and our customers’ experiences.
Essential Job Functions
* Fluent verbal and written communication skills (speaks/writes/reads English & Japanese language fluently) to support Shockwave customer service providers, customers and sales/clinical representatives over phone and email
* Communicate with Shockwave customers and sales/clinical representatives over phone and email.
* Maintain and improve customer service experiences for Japanese and International customers.
* Ensure successful processing of sales orders through the Japan third-party logistics group and work with customers in the event of issues or discrepancies
* Handle various order types, including but not limited to evaluations, consignments, warranty/complaints, and Free of Charge (FOC) orders, ensuring they are processed by the third-party customer service group and following up to confirm correct shipment.
* Deliver accurate and timely sales data reports to the organization on a daily, weekly, and monthly cadence.
* Maintain complete and accurate customer data across systems while collaborating with the US team to establish new accounts and ensure accurate translation into English and Japanese.
* Act as a back-up for the Customer Success Manager to assist with overseeing the 3rd party customer service team, providing guidance, coaching and training as needed
* Monitor order system errors in Salesforce and Oracle, as well as integrations, and provide quick resolution to ensure uninterrupted order flow daily.
* Develop/participate in continuous improvement projects to support appropriate automation and upkeep of processes and systems.
* Work cross-functionally with the clinical, sales, marketing, field inventory and operations teams as needed o...
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Type: Permanent Location: Chuo-ku, JP-13
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:48
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Writing
Job Category:
Professional
All Job Posting Locations:
Cincinnati, Ohio, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Sr Analyst, Medical Writing to be based in Cincinnati, OH.
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Job Responsibilities:
* Write, review, and revise technical documents including user manuals, standard operating procedures (SOPs), packaging inserts, service manuals, and training materials.
* Collaborate with R&D, quality assurance, regulatory affairs, and engineering teams to gather technical information.
* Ensure all documentation complies with applicable global regulatory standards such as FDA, ISO 13485, and MDR.
* Translate complex technical information into clear, concise, and user-friendly language for diverse audiences.
* Maintain and update existing documents to reflect product changes, improvements, and regulatory updates.
* Responsible for releasing document part numbers through Product Lifecycle Management (PLM) system
* Generated technical content for responsible product
* Facilitate the translation of the English content into the required languages
* Administrator for CCMS, DITA authoring tool, including Acrolinx integration
* Contributed to shaping the voice and style of the documentation set and establishing the product taxonomy
* Collaborate with cross-functional teams to restructure IFU templates for improved scalability and translation efficiency
* Mentor other writers on planning, outlining, and delivering use-case scenarios in XML and topic- based (DITA) format
* Accountable/responsible for working with labeling execution planning to align label development project plans with the project team schedules, escalating to resolve capacity constraints through prioritization, augmenting capacity or relieving project timing as aligned with project team and business units.
Qualifications:
* Bachelors Degree
* 6-8 Years Work Experience
* Demonstrated track record of Project Management
* Demonstrated ability to manage several pro...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:39
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Risk Management
Job Category:
Professional
All Job Posting Locations:
IN004 Bangalore
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where sophisticated diseases are prevented, treated, and cured, where treatments are more inquisitive 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/.
J&J Innovative Medicine Principal Operations belongs to the Innovative Medicine Companies of Johnson & Johnson.
J&J IM Principal Operations is a global organization located in USA, Belgium, Ireland, The Netherlands, Singapore, and Switzerland.
Within J&J IM Principal Operations, our mission is to provide diligent stewardship of the Innovative Medicine business model, by protecting and optimizing the product intellectual property (IP) structures in close collaboration with J&J Innovative Medicine Commercial, R&D, Supply Chain, Tax and Treasury.
Currently we are looking for “IMPO UAM Authorization Analyst” to join the J&J Innovative Medicine Principal Operations organization in “Bengaluru, India
Role Purpose:
The purpose of the role is charged with fortifying user access security and compliance across global SAP S4 systems, while driving strategic UAM initiatives to support organizational growth and technological for business adaptation purposes.
J&J Innovative Medicine (IM) Transcend is a global, multi-year end-to-end business transformation program aimed at modernizing foundational business processes through the implementation of SAP S/4 HANA.
This program focuses on core functionalities related to SAP Manufacturing, Order to Cash, Procure to Pay, and Finance processes.
The IMUAM team plays a crucial role in ensuring security requirements are crafted and implemented compliantly within this program.
Key Responsibilities:
* Drive security workshops to collect business and compliance requirements for role design, ensuring validation post-build for our S4 HANA Roles and Authorization requirement.
* Develop UAM strategies focusing on composite roles, Fiori tiles, business roles/user personas, and data security/UI mas...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2025-09-10 08:21:14
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Global Source to Pay Supplier Enablement Team Leader
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
In this role, you will:
* Lead and inspire a team of Supplier and Catalog Enablement professionals, fostering a high-performance culture across regions and shifts.
* Provide strategic direction, coaching, and development to team members, ensuring delivery against KPIs and career growth objectives.
* Oversee daily operations, ensuring timely execution of Coupa onboarding and enablement processes across EMEA and beyond.
* Serve as the central communication hub, aligning team activities with organizational goals and resolving challenges proactively.
* Drive continuous improvement initiatives, standardizing processes and enhancing efficiency in line with global transformation plans.
* Collaborate with key stakeholders to identify operational gaps, implement sustainable solutions, and maintain up-to-date documentation.
* Lead cross-regional projects, delivering scalable improvements across the Source-to-Pay (S2P) landscape.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do 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 manager roles, you’ll focus on winning with consumers and the market, while putti...
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Type: Permanent Location: Krakow, PL-MA
Salary / Rate: Not Specified
Posted: 2025-09-09 08:25:23
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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 Assurance
Job Category:
Professional
All Job Posting Locations:
Gent, East Flanders, Belgium
Job Description:
Position Title: QA Associate, CAR-T Europe (weekend)
Johnson & Johnson (J&J) is recruiting a QA Associate for the CAR-T hub in Europe.
The position will be based in Ghent Belgium.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, J&J has build two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories are operating from the existing J&J Beerse site. CAR-T investigational medicinal and commercial CAR-T products are manufactured in the Ghent facilities.
In this role, you are reporting in the J&J QA CAR-T organization and work closely with your peers from Material Science and Technology, Operations and Quality Control.
The QA Associate, CAR-T Europe (weekend) is responsible that product and process related investigations, complaints, batch review and release activities are properly handled on time and in line with all ATMP/GMP requirements.
This position will involve working in a weekend shift (6AM - 6PM).
Major Responsibilities:
Investigation Support: Provide technical, quality, and compliance expertise to support in-depth investigations related to deviations, complaints, and other quality issues to ensure timely resolution.
Deviations and Complaints Management: Ensure that deviations and complaints are promptly and thoroughly investigated, with particular attention to those that may affect patient safety or product supply.
Escalate issues that could have significant impacts on quality.
CAPA Management: Ensure that appropriate corrective and preventive actions (CAPAs) are identified and implemented in response to investigations, especially those with potential impacts on product quality and patient safety.
Inspection and Audit Support: Assist in the preparation, execution, and follow-up of internal and external inspections and audits to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements.
Quality Oversight Participation: Contribute to the quality oversight programs by providing documented QA approv...
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Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:13
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Your Job
We are seeking a PAC Specialist to join our Political Affairs Team.
The PAC Specialist manages the day-to-day administrative operations of Koch's political activity including KOCHPAC membership and contributions as well as playing a key role in maintaining compliance.
In doing so, the PAC Specialist is responsible for the efficient and effective operations of the PAC and is essential to its success.
This position requires travel of approximately 5-10%.
For this role, we anticipate paying $70,000 - $90,000 per year.
Our Team
We work to create the best possible public sector environment for Koch companies to create value, consistent with Principle Based Management™, by helping elect lawmakers who advance market-based policies.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have any questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
What You Will Do
* Report to the Political Director and work closely with PAC Director.
* Be responsible for all aspects of PAC membership and receipts management including timely management of incoming pledge changes, receipts, and reconciliation, membership additions and changes, as well as engagement with payroll, HR and compliance.
* Manage intake, processing and distribution of all federal and state disbursements.
* Manage the PAC database while working with outside consultants and internal partners to ensure accurate data on PAC-eligible employees and follow best practices and data retention requirements.
* Manage payments for PAC operations.
* Assist Political Director with PAC budget development, contribution analysis and support throughout the election cycle.
* Track and analyze membership and pledge data to assist the PAC Director in developing fundraising campaigns and engagement strategies to grow PAC membership and receipts.
* Support the PAC Director with internal PAC events, communications, and donor engagement.
* Manage company's GOTV efforts, including developing election communications.
* Maintain the PAC and GOTV websites, working with the website vendor.
* With the Federal Affairs Specialist, manage the political events calendar for the federal affairs team.
Who You Are (Basic Qualifications)
* Relevant experience in campaign and/or political fundraising or demonstrated equivalency of experience and/or education.
* Knowledge of and interest in Congress and the political process, or congressional office experience.
* Demonstrated ability to independently manage tasks and projects, including...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2025-09-07 08:14:12
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Your Job
We are seeking a PAC Specialist to join our Political Affairs Team.
The PAC Specialist manages the day-to-day administrative operations of Koch's political activity including KOCHPAC membership and contributions as well as playing a key role in maintaining compliance.
In doing so, the PAC Specialist is responsible for the efficient and effective operations of the PAC and is essential to its success.
This position requires travel of approximately 5-10%.
For this role, we anticipate paying $70,000 - $90,000 per year.
Our Team
We work to create the best possible public sector environment for Koch companies to create value, consistent with Principle Based Management™, by helping elect lawmakers who advance market-based policies.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have any questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
What You Will Do
* Report to the Political Director and work closely with PAC Director.
* Be responsible for all aspects of PAC membership and receipts management including timely management of incoming pledge changes, receipts, and reconciliation, membership additions and changes, as well as engagement with payroll, HR and compliance.
* Manage intake, processing and distribution of all federal and state disbursements.
* Manage the PAC database while working with outside consultants and internal partners to ensure accurate data on PAC-eligible employees and follow best practices and data retention requirements.
* Manage payments for PAC operations.
* Assist Political Director with PAC budget development, contribution analysis and support throughout the election cycle.
* Track and analyze membership and pledge data to assist the PAC Director in developing fundraising campaigns and engagement strategies to grow PAC membership and receipts.
* Support the PAC Director with internal PAC events, communications, and donor engagement.
* Manage company's GOTV efforts, including developing election communications.
* Maintain the PAC and GOTV websites, working with the website vendor.
* With the Federal Affairs Specialist, manage the political events calendar for the federal affairs team.
Who You Are (Basic Qualifications)
* Relevant experience in campaign and/or political fundraising or demonstrated equivalency of experience and/or education.
* Knowledge of and interest in Congress and the political process, or congressional office experience.
* Demonstrated ability to independently manage tasks and projects, including...
....Read more...
Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-09-07 08:14:12
-
Your Job
We are seeking a PAC Specialist to join our Political Affairs Team.
The PAC Specialist manages the day-to-day administrative operations of Koch's political activity including KOCHPAC membership and contributions as well as playing a key role in maintaining compliance.
In doing so, the PAC Specialist is responsible for the efficient and effective operations of the PAC and is essential to its success.
This position requires travel of approximately 5-10%.
For this role, we anticipate paying $70,000 - $90,000 per year.
Our Team
We work to create the best possible public sector environment for Koch companies to create value, consistent with Principle Based Management™, by helping elect lawmakers who advance market-based policies.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have any questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
What You Will Do
* Report to the Political Director and work closely with PAC Director.
* Be responsible for all aspects of PAC membership and receipts management including timely management of incoming pledge changes, receipts, and reconciliation, membership additions and changes, as well as engagement with payroll, HR and compliance.
* Manage intake, processing and distribution of all federal and state disbursements.
* Manage the PAC database while working with outside consultants and internal partners to ensure accurate data on PAC-eligible employees and follow best practices and data retention requirements.
* Manage payments for PAC operations.
* Assist Political Director with PAC budget development, contribution analysis and support throughout the election cycle.
* Track and analyze membership and pledge data to assist the PAC Director in developing fundraising campaigns and engagement strategies to grow PAC membership and receipts.
* Support the PAC Director with internal PAC events, communications, and donor engagement.
* Manage company's GOTV efforts, including developing election communications.
* Maintain the PAC and GOTV websites, working with the website vendor.
* With the Federal Affairs Specialist, manage the political events calendar for the federal affairs team.
Who You Are (Basic Qualifications)
* Relevant experience in campaign and/or political fundraising or demonstrated equivalency of experience and/or education.
* Knowledge of and interest in Congress and the political process, or congressional office experience.
* Demonstrated ability to independently manage tasks and projects, including...
....Read more...
Type: Permanent Location: Wichita, US-KS
Salary / Rate: Not Specified
Posted: 2025-09-07 08:14:11
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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!
* Aufbereitung virushaltiger Vorstufen, Formulierung und aseptische Abfüllung von Impfstoffen
* Gefriertrocknung von Impfstoffen und Verbördeln von Impfstoffflaschen
* Vorbereiten und Bedienen von Produktionsanlagen im Produktionsbereich Abfüllung
* Aseptisches Arbeiten im Reinraum
* Durchführung von Reinigungs-, Vor- und Nachbereitungsarbeiten
* GMP-gerechte Dokumentation
* Einsatz zur Aufrechterhaltung der Produktion im Schicht-/Wechseldienst, auch nach Dienstschluss und am Wochenende
* Umgang mit MS-Office-Programmen
* Buchung von Prozessaufträgen im SAP-System
* Flexibler Einsatz auch in anderen Unternehmens-/Produktionsbereichen u.a.
in der bakteriellen und viralen Produktion, Central Service, L&P, Hygiene Monitoring, wenn dies aus betrieblichen Gründen notwendig ist
Fachliche Qualifikationen und persönliche Voraussetzungen:
* Abgeschlossene Ausbildung im pharmazeutisch-, biologisch- oder chemisch-technischen Bereich oder vergleichbare Qualifikation
* Produktionserfahrung im GMP Umfeld wünschenswert
* Sehr hohes Hygienebewusstsein
* Arbeiten im Team
* Bereitschaft zum flexiblen Arbeitseinsatz sowie Einsatzbereitschaft an Wochenenden
* Gute Deutsch- und Englischkenntnisse in Wort und Schrift
* Strukturierte und flexible Arbeitsweise, Zeit- und Selbstorganisation
Was wir anbieten:
* Interessantes und abwechslungsreiches Arbeitsumfeld in einem modernen und wachsenden globalen Unternehmen der Pharmaindustrie
* Raum für Initiative und Flexibilität
* Spannende Entwicklungsmöglichkeiten
* Firmenfitnessprogramm
* Verpflegungsgeld
* Vorteile für Unternehmen
* Teamevents
* Bis zu 30 Tage Urlaub
* Sonderurlaubstage (Hochzeit, Arbeitsjubiläen etc.)
* Attraktive Vergütung gemäß Betriebstarifvertrag inklusive Weihnachts- und Urlaubsgeld
* 38 Stunden/Woche
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender iden...
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Type: Permanent Location: Cuxhaven, DE-NI
Salary / Rate: 3502
Posted: 2025-09-03 09:11:07
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Professional
All Job Posting Locations:
Albany, New York, United States of America, Buffalo, New York, United States, Danvers, Massachusetts, United States of America, New York, United States of America, Rochester, New York, United States
Job Description:
Johnson & Johnson is recruiting for a Surgical Account Manager or an Associate Surgical Account Manager, based on experience, to be in Rochester, Buffalo, Albany-New York, United States.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Job Responsibilities:
* Gain distribution and utilization of the Impella 5.5 (left sided treatment)
* Gain distribution and utilization of the Impella RP (right sided treatment)
* Manage EXCEL sites and clinicals on new Surgery, Heart Failure, ECMO technologies
* Work collaboratively within the area to achieve quarter over quarter growth
* Drive excitement and vision of heart recovery solutions with existing devices and future technologies
* Call point(s): Cardiac Surgeons, Heart Failure Cardiologists, “Heart Team” (to include Interventional Cardiologists, Intensivists, & Perfusionists)
* Staff major conferences: HFSA, AHA, STS, AATS, and ISHLT
* Staff local heart failure symposiums
* Build surgical vertical in established Impella programs – Full product portfolio
Qualifications:
* Bachelor’s degree required
* A minimum of 10+ years experience of cardiac surgery and/ or combined cardiology medical device sales required for the Surgical Account Manager level
OR
* A minimum of 5+ years experience of cardiac surgery and/ or combined cardiology medical device clinical or sales required for the Associate Account Manager level
* Proven track record of selling in an operating room is required
* A proven track record in leading and motivating teams to successfull...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-08-30 08:18:54
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Westminster Oaks is seeking a Resident Lifestyle Assistant to plan, develop, and direct the overall operation of the resident services department in accordance with regulatory guidelines and our established policies and procedures.
This position plays a key role in enhancing resident engagement through thoughtfully designed programs and events, many of which rely on technology for successful execution.
At the discretion of Administration, the Resident Lifestyle Facilitator Assistant may be required to act as the interim Resident Lifestyle Facilitator in the event of their absence or a vacant position.
Comply with all applicable rules, policies, standards, and guidelines related to employment with Westminster and its communities.
Facilitate Resident Services programs and activities as designated by the department manager.
This may include teaching classes to residents and supporting a variety of enrichment activities.
Strong technical skills are required, including proficiency with computers, software applications, and audiovisual equipment.
The ability to operate and troubleshoot AV systems—such as microphones, projectors, speakers, and video conferencing tools—is essential to ensure smooth delivery of presentations, entertainment, and educational sessions.
Escort residents to group outings/activities and assist with setup and operation of audio/video components for events and programs.
Preference will be given to candidates with a strong background in AV technology, including experience in setting up and managing multimedia presentations, live-streaming, and digital content creation.
The above job description is not to be construed as a complete listing of the assignments and responsibilities assigned to any employee; nor are such assignments restricted to those precisely listed in the description. This job description may change from time to time as the needs of the organization change.
EOE, DFWP, "We honor those who serve."
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: tallahassee, US-FL
Salary / Rate: Not Specified
Posted: 2025-08-27 08:54:03
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Geel, Antwerp, Belgium
Job Description:
Over Innovatieve Geneeskunde
Onze expertise op het gebied van innovatieve geneeskunde wordt geïnformeerd en geïnspireerd door patiënten, wier inzichten onze wetenschappelijke vooruitgang voeden.
Mensen met een visie zoals jij werken in teams die levens redden door de medicijnen van morgen te ontwikkelen.
Sluit je bij ons aan om behandelingen te ontwikkelen, genezingen te vinden en de weg te banen van het laboratorium naar het dagelijks leven, terwijl we patiënten bij elke stap van het proces ondersteunen.
Ga voor meer informatie naar https://www.jnj.com/innovative-medicine
We zijn op zoek naar het beste talent voor Chemisch Magazijn Operator Volcontinue in Geel, Belgie
Heb jij ervaring in een geautomatiseerde magazijn en een passie voor innovatie? Als je ja zegt, dan zijn wij op zoek naar jou!
Dit betreft een tijdelijk contract met kans op verlenging.
U bent verantwoordelijk voor:
* Verwerking van binnenkomende en uitgaande leveringen.
* Voorbereiding van orders voor productie.
* Nauwkeurig afwegen van grondstoffen en producten, inclusief gevaarlijke stoffen.
* Controle van productieorders voor distributie.
* Logging van werkzaamheden volgens procedures.
* Zorg dragen voor orde en netheid in het magazijn, zowel als verbeteringen aandragen.
* Naleven van veiligheidsinstructies bij het werken met chemische stoffen.
* Transport van goederen met reach- en heftruck.
Kwalificaties/Vereisten:
* Hoger Middelbaar Onderwijs of gelijkwaardig door ervaring.
* Minimaal 3 jaar ervaring in een commerciële, distributie of industriële omgeving.
* Vereiste taal: Nederlands
* Technische scholing en kennis van SAP, Excel en Word zijn een plus.
* Bereidheid om in een volcontinu ploegen systeem te werken.
* Bereidheid om te werken met complexe procedures.
* Ervaring met besturingssystemen en digitalisatie.
* Senior profiel die gaat voor verbetering en zelfstandig zorg dragen.
* Affiniteit met digitale veranderingen.
Bij Johnson & Johnson willen we dat elke kandidaat zich ondersteund voelt tijdens het sollicitatieproces.
Ons doel is om de ervaring duidelijk, eerlijk en respectvol te maken voor jouw tijd.
Dit kun je verwachten:
* Beoordeling van d...
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Type: Permanent Location: Geel, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-08-27 08:30:57
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Agile Procurement Project Lead
Job Description
Agile Procurement Project Lead (12-month Fixed Term Contract)
Location: Walton Oaks, Surrey, UK/ Other EMEA locations can be considered
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.
As a Project Manager in the Agile Procurement Team, you'll serve as a variable resource within the Global Procurement Centre of Expertise (COE).
This role is committed to unlocking incremental value and accelerating delivery of critical negotiations & procurement projects.
You'll deliver high visibility, high ROI projects across categories in collaboration with the Agile Procurement Team, category managers and business leaders.
You'll utilize skills & experience in strategic sourcing, project management, and problem solving / critical thinking.
This is an individual contributor role with the Agile Procurement team, reporting to the Director of Agile Procurement & Analytics.
In this role, your responsibilities will include but not be limited to:
* Provide global and regional category teams with analytics, RFP/RFQ/RFI content development, and sourcing execution.
* Deliver robust analytical support (should cost, scenario modelling) for market events.
* Accelerate value delivery on key sourcing efforts by adding analytics, rigor and horsepower by utilizing a broad set of analytical capabilities.
* Apply agile principles and problem-solving frameworks to lead projects, structure sourcing events and to recommend best practices.
* Drive incremental value in current and future sourcing efforts by deploying critical thinking and problem-solving tools.
* Build knowledge of e-sourcing tools & leverage capabilities for value delivery (Coupa & Coupa Sourcing Optimization).
* Support category strategy development and other strategic projects
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
...
....Read more...
Type: Permanent Location: Tadworth, GB-SRY
Salary / Rate: Not Specified
Posted: 2025-08-23 08:44:48
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Your Role
Koch Engineered Solutions (KES) is looking for an experienced Senior Communications Manager to own internal communications platforms for its global businesses.
The Senior Communications Manager is responsible for developing and executing strategic plans and providing consulting expertise across businesses, capabilities and operations, as well as supervising the communications team.
This position is located in Wichita, Kansas.
In this role, you will contribute to organizational alignment and action by partnering closely with business leaders to advance understanding and connection to the vision, our Principle Based Management™ philosophy and culture, our priorities, and key initiatives.
You and your team will craft and deliver presentations, town halls, videos, and other content for internal audiences.
You will also own the KES Corporate Brand, deploying it internally and externally to position KES as a trusted partner to customers and an employer of choice in the market.
If any of the above sounds like you, let's talk!
This position is not eligible for VISA Sponsorship.
Our Team
We are an in-house Marketing & Communication capability supporting all KES business units.
We contribute to business outcomes through close partnership and collaboration with leadership, HR and supervisors.
We leverage the strengths, talents, and experience of our team and trusted third-party agencies to design and execute targeted marketing plans.
KES is a global industrial solutions partner, encompassing a diverse network of specialized businesses, each a leader in its respective field.
We deliver tailored solutions to optimize performance and drive ongoing progress across the industrial spectrum including mass transfer; combustion and emissions controls; process technology development and licensing; full engineering, procurement and construction; asset integrity; utility-scale solar and energy storage.
Backed by the resources and knowledge of Koch, Inc., we foster a culture of collaboration, where expertise across various domains converges to solve our customers' challenges.
More information is available at KochEngineeredSolutions.com .
What You Will Do:
Here are some ways you'll get to use and grow your knowledge and skills:
* Design and implement strategic communications programs internally to business and manufacturing audiences to maximize employee understanding of KES and its subsidiary business units' visions and goals, compliance, and Principle Based Management™ philosophy.
* Guide strategic use of communications vehicles and channels to advance business priorities in support of the vision.
* Develop strategies and platforms that empower supervisors to build more meaningful connections with their teams.
* Advise on issues, attitudes, and opinions both inside and outside the company that could affect business results or reputation.
* Supervise the KES Communications Team, driving key priorities while developing ...
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Type: Permanent Location: Wichita, US-KS
Salary / Rate: Not Specified
Posted: 2025-08-19 08:26:58
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a Technical Writer to join our Technical Services Team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Technical Writer reports to the Director of Technical Services and Validation.
The essential job function is to assume responsibility for all documentation and procedural activities associated with commercial production and technical transfers, as well as support documentation needs of the R&D scientists. It includes monitoring of existing documents (including, but not limited to: Batch Records, SOPs, OIMs), identifying opportunities for improvement, and implementing both process and/or procedural improvements to further the efforts in the Manufacturing group to continuously improve. It also includes project execution within the department, such as product transfers or changes, in addition to other daily functions needed or requested by the Director of Validation and Technical Services.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
* Provide documentation services to the Technical Services department including writing, revising, formatting, processing, filing, and maintaining documents, including electronic files. These documents include, but are not limited to batch production records, SOPs, protocols, and reports.
* Be able to draft incident reports, investigation reports, or other quality event (QE) reports.
* Support Quality Systems for the Technical Services Department, including CAPA, Change Control, QE tracking/trending.
* Work with technical experts to identify and document appropriate Corrective Action, Preventative Action (CAPA) as needed.
Responsible for completion of appropriate CAPA documentation.
* Act as Electronic Quality Documentation Management System Subject Matter Expert (SME) for the department, assisting and training others as needed.
* Responsible for the SOP biennial review process for Technical Services, including SOP revisions within the establis...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-08-19 08:20:41
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Game Night Communications Assistant
Location: San Antonio, TX / Non-Exempt
At Spurs Sports & Entertainment (SS&E), we work in service of something bigger than ourselves. To us it is so much more than just a game or concert. It takes all the members of our Spurs team to harness the power of sports and entertainment to create moments that excite, memories that endure, and connections that strengthen our community.
SS&E owns and operates the San Antonio Spurs (NBA), Austin Spurs (NBA G-League), and the San Antonio FC (USL), and manages day-to-day operations of the Frost Bank Center, Toyota Field, and STAR Complex.
We know that our people are our greatest asset as an organization.
We aspire to provide our teams with meaningful work, to live our values - Integrity, Success & Caring – day-to-day in what we do and foster an inclusive culture for our 1K+ employee workforce.
The San Antonio Spurs are looking for several game night communication assistants to join our family!
In this role, you will be responsible for assisting with the game night Public Relations (PR) efforts for the San Antonio Spurs during the 2025-26 NBA season.
You will be provided with hands-on experience within a professional sports media relations environment.
The position will provide an individual who desires a career in sports information or media relations with an opportunity to learn the business side of sports and media while gaining valuable career experience, building a portfolio and enjoying networking opportunities in the process.
What You’ll Do:
* Attend select Spurs home games (Approximately 4 p.m.
to 11 p.m.
for a 7 p.m.
game)
* Assist with setting up press areas, including labeling seats and setting out monitors and printers
* Distribute media credentials and assist with media check-in
* Record and transcribe pre-game and postgame quotes
* Manage media dining check-in
* Distribute in-game and postgame statistics to media members
* Digitization of postgame materials and historical documents
* Help all local and national media as needed
* Assist Spurs PR staff as needed
Who You Are:
* High School Diploma or GED
* Currently enrolled in college with an interest in public relations/communications preferred
* Strong quote-taking and transcribing skills
* Ability to meet deadlines in short, high-pressure situations
* Outstanding communication skills (both verbal and written)
* Ability to manage multiple projects simultaneously
* Demonstrate proficient computer skills, including but not limited to, MS Word
* Ability to work at least 15-20 hours per week during the NBA Season and non-traditional hours (including nights and weekends)
Physical Requirements:
* Standing for extended periods of time.
* Constantly walking to accomplish tasks, particularly walking around the arena to service media seating locations.
In every positi...
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Type: Permanent Location: San Antonio, US-TX
Salary / Rate: 13
Posted: 2025-08-13 08:48:12
