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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 Manufacturing
Job Sub Function:
Multi-Family Supply Chain Manufacturing
Job Category:
People Leader
All Job Posting Locations:
Juarez, Chihuahua, Mexico, São José dos Campos, São Paulo, Brazil
Job Description:
Job Description
Johnson & Johnson is currently recruiting for a Director of Engineering, Global Technical Operations (GTO) primarily based in Raritan, NJ with consideration for J&J MedTech Sites in the US and LATAM.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
[United States & Puerto Rico] - Requisition Number: R-030387
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Position Overview:
We are seeking a skilled and experienced leader to serve as the Director of Engineering, Global Technical Operations (GTO) for our Ethicon Wound Closure Healing (WCH) platform.
In this role, you will lead the GTO function across a network of five manufacturing locations in the Americas, focusing on the development of polymer and metals component manufacturing, packaging, and sterilization technologies.
You will be a key member of the Americas Platform E2E Leadership Team and the Wound Closure Global Technical Operations leadership team, contributing to the strategic direction and technical excellence of the Med Tech Surgery manufacturing network.
Key Responsibilities:
* You will be accountable for developing and executing the engineering strategy that enhances operational efficiency and fosters technological innovation across all sites.
* Provide leadership and guidance to engineering teams across the network, fostering professional development, collaboration, and a high-performance culture.
* Formulate and drive a comprehensive manufacturing strategic roadmap aligned with organizational goals, while leading efforts to optimize processes and cultivate a culture of continuous improvement.
* Provide strategic direction and comprehensive oversight of engineering teams responsible for the design, development, and testing of manufacturing technologies, ensuring alignment with best -in-class industry standards, regulatory requir...
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Type: Permanent Location: Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-09-06 08:19:33
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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:
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 – Micro analyst in an Early-Late shift or 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 Micro 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 environment 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 investigation records and CAPAs.
* Assist in the execution of internal audits.
* Provide input to functional laboratory meetings.
* Provide input and take actions as a QC representative at cross-laboratory meetings.
* You will work in an Early-Late or weekend shift regime.
Qualification and requirements:
* A minimum...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-06 08:19:30
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Technical Product Manager - Global Trade Compliance to be located in Titusville, NJ or Beerse, Belgium location.
This position has the potential to be located at another J&J facility within the United States for the right talent.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
United States/Titusville, NJ - Requisition Number: R-026664
Beerse, Belgium - Requisition Number: R-028152
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Innovative Medicine Transcend is a global business transformation program that will modernize our foundational transactional processes and harmonize them into one “clean” ERP as a standardized platform for growth and efficiency gains.
The program will simplify the Innovative Medicine ERP landscape from 7 platforms to 1, standardizing processes to drive a cost effective, fit for purpose digital backbone that will enable us to support the Innovative Medicines business with agility.
Additionally, the program will remediate the end-of-life system exposure that we risk towards the end of this decade.
This role will shape and deliver the Innovative Medicine global template for the Global Trade Compliance processes and enable new capabilities for emerging supply chain needs within IM E2E Supply Chain (R&D, Clinical and Commercial)
The position leads design and delivery of Global Trade Compliance capabilities in SAP S/4HANA and SAP GTS E4H and governs the J&J IM template while driving the capabilities' evolution through the deployments within the GTS domain and must connect across functional domains to enable an End-to-End integrated solution.
The Technical Product Manager - Global Trade Compliance will be an active member of the IM Supply Chain JJT team, driving global standardization within Innovative Medicines ERP technology solutions and taking ownership of the corresponding GTS so...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-06 08:19:27
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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:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
Professional
All Job Posting Locations:
Norderstedt, Schleswig-Holstein, Germany
Job Description:
Bei Johnson & Johnson glauben wir, dass Gesundheit alles ist.
Unsere Stärke im Bereich der Gesundheitsinnovation befähigt uns, eine Welt zu schaffen, in der komplexe Krankheiten verhindert, behandelt und geheilt werden und Behandlungen intelligenter, weniger invasiv und Lösungen persönlich sind.
Durch unsere Expertise in innovativer Medizin und MedTech sind wir in der einzigartigen Position, innovative Lösungen in das gesamte Spektrum der Gesundheit zu injizieren, um die Durchbrüche von morgen zu erzielen.
Wir verbinden Wissenschaft, Technologie und Entschlossenheit, um die Gesundheit der Menschheit tiefgreifend zu verbessern.
Erfahren Sie mehr unter https://www.jnj.com/
Über MedTech
Wir arbeiten seit einem Jahrhundert an der Seite von Ärzten und Patienten, um das Gesundheitswesen immer wieder aufs Neue zu verbessern und zu optimieren sowie neu zu denken. Unser J&J-MedTech-Portfolio wird von Innovationen geprägt, die Barrieren an der Schnittstelle zwischen Biologie und Technologie aus dem Weg räumen.
Gemeinsam entwickeln wir die nächste Generation intelligenter, weniger invasiver und personalisierter Lösungen, um die größten und komplexesten gesundheitlichen Herausforderungen für Menschen auf der ganzen Welt zu bekämpfen.
Begleiten Sie uns auf unserem Weg, während wir Medizinprodukte weiterentwickeln und den Übergang von der Forschung ins echte Leben ermöglichen – immer im engen Austausch mit unseren Patienten, um sie bei jedem Schritt zu unterstützen.
Weitere Informationen finden Sie unter https://www.jnj.com/medtech
Interne Stellenausschreibung 04.09.2025 - 19.09.2025
Optionen für Remote-Arbeit können je nach Fall geprüft werden und müssen von der Firma genehmigt werden.
Wir suchen das beste Talent für die Position des
HEALTH ECONOMICS & MARKET ACCESS MANAGER - Surgery
STELLENPROFIL
Als Fachverantwortlicher für den Bereich Surgery wird der Health Economics & Market Access Manager in enger Zusammenarbeit mit Marketing, Vertrieb und der lokalen/regionalen HEMA Organisation Strategien entwickeln und umsetzen, die den Marktzugang und den Wettbewerbsvorteil von Johnson & Johnson-Produkten in einem wertorientierten Gesundheitsmarkt nachhaltig gewährleisten.
AUFGABEN
* Aufbereitun...
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Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-09-06 08:19:21
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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:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
Wilson, North Carolina, United States of America
Job Description:
The Johnson & Johnson Family of Companies is currently recruiting for an Environmental, Health & Safety (EHS) Specialist! This position will be located in Wilson, NC.
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 Summary:
The EHS Specialist is responsible for supporting and delivering the J&J IMSC Wilson EHS requirements incl.
for instance Industrial Hygiene, Bio Safety, Chemical Safety, Laboratory Safety, and linked Risk Assessment processes in compliance with Johnson & Johnson (J&J) requirements and US Code requirements, project design and delivery process in support of J&J's North Carolina Biologics expansion program etc.
Key Responsibilities:
* Under direct supervision, support biosafety, general safety, industrial hygiene and chemical management programs in a laboratory setting.
* Develop site-specific procedures and programs based on corporate guidance, regulatory standards, and best practices.
* Partners with associates at all levels including frequent interaction with middle and senior management at the business location and occasional interaction with regulatory authorities.
* Provide technical support and guidance on EHS standards and best practices to various facility stakeholders.
* Participating in and support EHS projects, Risk Assessments, and ensure identified action are incorporated into the site tracking process.
* Document all EHS reviews at various stage-gates and manage measures to achieve action closure in a timely manner.
* Ensure EHS compliance and laboratory safety are integrated into design processes from the earliest stages to prevent rework and ensure compliance.
* Participate in all stages of the vendor technical re...
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Type: Permanent Location: Wilson, US-NC
Salary / Rate: Not Specified
Posted: 2025-09-06 08:19:15
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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 Engineering
Job Sub Function:
Multi-Family Supply Chain Engineering
Job Category:
People Leader
All Job Posting Locations:
Cornelia, Georgia, United States of America, Juarez, Chihuahua, Mexico, Raritan, New Jersey, United States of America, San Angelo, Texas, United States of America, San Lorenzo, Puerto Rico, United States of America, São José dos Campos, São Paulo, Brazil
Job Description:
Johnson & Johnson is currently recruiting for a Director of Engineering, Global Technical Operations (GTO) primarily based in Raritan, NJ with consideration for J&J MedTech Sites in the US and LATAM.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
[ILATAM] - Requisition Number: [Insert Requisition Number 1]
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Position Overview:
We are seeking a skilled and experienced leader to serve as the Director of Engineering, Global Technical Operations (GTO) for our Ethicon Wound Closure Healing (WCH) platform.
In this role, you will lead the GTO function across a network of five manufacturing locations in the Americas, focusing on the development of polymer and metals component manufacturing, packaging, and sterilization technologies.
You will be a key member of the Americas Platform E2E Leadership Team and the Wound Closure Global Technical Operations leadership team, contributing to the strategic direction and technical excellence of the Med Tech Surgery manufacturing network.
Key Responsibilities:
* You will be accountable for developing and executing the engineering strategy that enhances operational efficiency and fosters technological innovation across all sites.
* Provide leadership and guidance to engineering teams across the network, fostering professional development, collaboration, and a high-performance culture.
* Formulate and drive a comprehensive manufacturing strategic roadmap aligned with organizational goals, while leading efforts to optimize processes and cultivate a culture of continuous improvement.
* Provide strategic direction and comprehensive oversight of engineerin...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-06 08:19:05
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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:
Position: Graduate Quality Control Analyst
Start Date: September 2026
Location: Cork, Ireland
Johnson & Johnson Innovative Medicine established its operation in Ringaskiddy in 2005 on a 100-acre site with an investment of €500 million.
For more than 25 years we have been a global leader in the field of biomedicines, particularly in groundbreaking monoclonal antibody technology, an approach to producing medicines that launched a new generation of products to treat immune related diseases such as rheumatoid arthritis and plaque psoriasis.
The facility in Ringaskiddy is fully operational and currently expanding its operations to continue focusing on producing biomedicines for both the treatment of immune related diseases and new and creative cancer treatments.
ABOUT THE JOHNSON & JOHNSON GRADUATE PROGRAMME
The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites.
It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business.
THE SUCCESSFUL CANDIDATE WILL HAVE THE OPPORTUNITY TO:
* Develop relevant technical skills within their area of expertise.
* Experience cross functional exposure both on site and within Campus Ireland.
* Participate in regular one to ones and feedback to support your on-going development.
* Engage in personal development and effectiveness training.
* Develop influencing & communication skills.
* Gain Project Management experience.
* Learn new and innovative technologies.
* Gain exposure to Senior Management Team.
* Participate in continuous professional development program with a recognised qualification.
JOB PURPOSE:
We have an exciting opportunity for a QC Analyst on the Ireland Graduate Program.
This individual will be responsible for carrying out tasks and projects related to the analysis of biotechnology products as required by Good Manufacturing practice (GMP).
The individual will participate in the delivery of lab testing efforts by using both existing and new procedures or processes to independently interpret data and identify and correct issues.
Proposes ideas and next steps...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-09-06 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:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
People Leader
All Job Posting Locations:
Anaheim, California, United States, Baltimore, Maryland, United States, Cincinnati, Ohio, United States of America, Danvers, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New York, New York, United States, Philadelphia, Pennsylvania, United States, Tampa, Florida, United States of America, Titusville, New Jersey, United States of America, Wilmington, Delaware, United States
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Technical Product Manager - Global Trade Compliance to be located in Titusville, NJ or Beerse, Belgium location.
This position has the potential to be located at another J&J facility within the United States for the right talent.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
United States/Titusville, NJ - Requisition Number: R-026664
Beerse, Belgium - Requisition Number: R-028152
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Innovative Medicine Transcend is a global business transformation program that will modernize our foundational transactional processes and harmonize them into one “clean” ERP as a standardized platform for growth and efficiency gains.
The program will simplify the Innovative Medicine ERP landscape from 7 platforms to 1, standardizing processes to drive a cost effective, fit for purpose digital backbone that will enable us to support the Innovative Medicines business with agility.
Additionally, the program will remediate the end-of-life system exposure that we risk towards the end of this decade.
This role will shape and deliver the Innovative Medicine global template for the Global Trade Compliance processes and enable new capabilities for emerging supply chain needs within IM E2E Supply Chain (R&D, Clinical and Commercial)
The position leads design and delivery of Global Trade Compliance capabilities in SAP S/4HANA and SAP GTS E4H and governs the J&J IM template while driving the capabilit...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-06 08:18:16
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Pharmaceutical Product R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
As a Senior Scientist within the Center for Computational Chemistry and Advanced Modelling, you play a pivotal role in reshaping how we develop small molecule medicine & therapies by leveraging mechanistic and data-driven modelling techniques.
We are seeking for a passionate modelling expert to join our team.
The successful candidate will work in interdisciplinary teams and collaborate closely with scientists at various stages of drug product development to contribute to delivering the most robust drug products.
They will use the currently established modelling methodologies to support new and ongoing projects and expand the general modelling capabilities further.
This is a fixed-term position until 20th of December 2027.
Role and responsibilities
* Identify the mechanisms governing drug product behaviour using underlying physical and chemical principles.
* In support of knowledge improvement and understanding, design relevant experimental designs which can be used to calibrate, build and/or expand mathematical models.
* Proactively identify new areas that could be solved using mathematical modelling or data-driven methods.
* Translate learnings and new insights into concrete and actionable recommendations for the drug product development portfolio.
* Interact and collaborate with scientists across discovery and development organizations, IT and statistics.
Qualifications
* A PhD in chemistry, physics, engineering, pharmaceutical sciences or related field, or equivalent advanced experience, is required.
– with focus in data driven research.
Required Experience and Skills
* Knowledge of either mathematical modelling, statistics or experimental design.
* Expertise in mechanistic/data-driven and/or statistical modelling of scientific processes and material attributes, preferably in a pharmaceutical context.
* Experience with at least one programming language such as Python, Julia, or R.
* Experience with data extraction, data preprocessing and data analysis.
* Any additional experience with algorithmic analyses or modelling techniques, such as model-based optimal design, Bayesian optimization, machine learning methods or cheminformatics is consi...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-06 08:18:02
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Analyst II, Global Data Manager
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 an Analyst II Data Manager in our Clinical Data Standards team, located in High Wycombe, United Kingdom (Hybrid: 3 days per week onsite).
In this role, you will provide oversight and accountability for data management activities across multiple trials of low to moderate complexity or for a single high-complexity trial.
The Analyst II Data Manager makes recommendations and influences decisions for specific trials or assignments while executing critical data management tasks and performing scientific data reviews.
You will analyse data and make informed recommendations under the guidance of your manager or the Data Management Leader (DML).
Your work will be received in broad terms, with oversight from the DML on an ongoing basis, and the amount of instruction will be limited, allowing for autonomy.
You will be responsible for:
* Taking a leadership role with external suppliers, trial customers, and other internal/external partners to establish, align, and confirm data management and/or clinical data management expectations to the business for assigned trial(s) to include but not limited to:
* Gathering and/or reviewing content and integration requirements for eCRF and other data collection tools.
* Establishing conventions and quality expectations for clinical data.
* Establishing expectations for dataset content and structure.
* Setting timelines and following up regularly to monitor the delivery of all data management milestones.
* Reviewing clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
* Ensuring compliance with regulatory guidelin...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-09-06 08:17:46
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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
Unsere Pharma-Vision
Medikamente schnell zu den Patienten zu bringen und das beste Ergebnis für unsere Kunden zu schaffen.
Das ist es, was uns in Sterile Drug Product Manufacturing (SDPM) in Mannheim antreibt.
So tragen wir auch dazu bei, bis 2029 unser Ziel zu erreichen: 20 bahnbrechende Medikamente zur Behandlung der Krankheiten mit der größten gesellschaftlichen Belastung bereitzustellen.
Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele große Hoffnung und Zuversicht und deswegen müssen wir anders denken und arbeiten.
Mit dem Patient im Fokus setzen wir auf eine neue Organisation und zwar #WIRGEMEINSAM in SDPM!
Deine Position
Als Quality Assurance Manager Sterile Filling förderst Du aktiv die Umsetzung unserer Lean-Mindset Kultur unter Berücksichtigung der Pharma Technical Operations (PT) Behaviors und Lean-Methoden und lebst diese vor. Du förderst die Harmonisierung und kontinuierliche Verbesserung einzelner Prozesse und Vorgehensweisen in Abstimmung und Koordination mit den anderen Value Streams am Standort.
Be a coach! Operatives und strategisches GMP-Coaching aller Funktionen innerhalb und bei Bedarf ausserhalb des Value Streams (VS) übernimmst Du ebenfalls im Zuge deiner Tätigkeit.
Für Deine Aufgaben bist Du primär in Mannheim vor Ort.
Deine Aufgaben
* Du unterstützt aktiv die Patientenversorgung mit kommerziellen und klinischen Arzneimitteln durch Sicherstellung einer GMP-konformen und termingerechten Freigabe von Arzneimittelchargen.
Die Berücksichtigung der gesetzlichen, regulatorischen und Roche internen Vorgaben sind Dir hierbei besonders wichtig
* Zusammenstellung, Prüfung und Bewertung von Herstelldokumenten aus der eigenen Produktion und von anderen Standorten
* Die Bearbeitung und Qualitätsbewertung komplexer Abweichungen und geplanter Events (Changes, CAPA) übernimmst Du selbständig und leitest und koordinierst bei Bedarf das lokale Triage Team zur Bearbeitung und Root-Cause-Analyse (RCA) von Abweichungen innerhalb des verantworteten Value Streams
* Du übernimmst die Bearbeitung und Koordination von Abweichungen und geplanten Events (Changes, CAPA) in Zusammenarbeit mit anderen Partnern im Netzwerk (Multisite)
* Du vertrittst die Qualitätsaspekte des Value Streams und unterstützt aktiv Audits und Selbstinspektionen und nimmst daran teil.
Zudem übernimmst du die fachliche Vertretung des Standorts in globalen Qualitätsgremien oder bei Behördenintera...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-09-06 08:16:21
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ERM is hiring Environmental Inspectors throughout the state of Virginia to oversee environmental compliance during the construction phase of Electric Transmission Utility projects.
The projects we work on and the services we provide demand teams of multiple disciplinary professionals working collaboratively to meet our clients’ needs.
This position is a full-time (40 hours + per week) limited-term role with a duration of 6 months, extendable.
RESPONSIBILITIES:
* The primary responsibilities of this field-based position include:
* Preparing documentation to support requests for variances from environmental permits.
* Preparing and conducting environmental training for construction personnel.
* Conducting field inspections, monitoring and field survey work as directed.
* Interacting with and serving as a point of contact with agency officials, regulatory agency staff, landowners, contractors, clients and other project members and conducting required agency notifications.
* Reviewing and implementing project documents and providing direction, support and critical judgment on environmental compliance issues.
* Providing technical leadership, support and direction to field staff. This includes the coordination of daily Environmental Inspector and Resource Monitor schedules and conducting morning construction meetings.
* Critically assessing environmental conditions in the field to evaluate potential environmental impacts from construction.
* Evaluating potential issues and concerns ahead of construction activities.
* Overseeing the proper implementation of mitigation measures.
* Conducting environmental sampling (hydrostatic test water, soil, etc.).
* Overseeing and verifying flagging of wetland boundaries, cultural and biological resources exclusion zones, refueling zones, etc..
* Inspecting and documenting compliance with a project's environmental requirements by preparing daily written inspection reports that provide up-to-date and consistent written and photo documentation of activities observed in the field.
* Participating in various construction meetings.
* Evaluating restoration activities.
* Performing additional tasks as assigned or required.
REQUIREMENTS:
The role of an Environmental Inspector requires meticulous oversight by highly skilled individuals stationed in the field throughout construction to ensure compliance with federal, state and local environmental regulations.
Qualifications of individuals to be considered will include:
* Experience working in and throughout Virginia.
+ Experience working with VA SWPP Guidelines
* BS or BA degree or a minimum of 5 years equivalent environmental inspection experience.
* An understanding of construction (e.g., pipelines, power lines, compressor/pumping stations, gas storage fields, wind farms, solar facilities, offshore facilities) gained through field experience.
* S...
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Type: Permanent Location: Richmond, US-VA
Salary / Rate: Not Specified
Posted: 2025-09-06 08:15:25
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PD&E Planner
Ardurra has an exciting opportunity for a Planner in our Project Development and Environment (PD&E) group in Orlando, Florida.
The position includes working with senior staff to prepare planning studies, alternative analyses, environmental impact assessments, and technical reports, including preparation of National Environmental Policy Act (NEPA) documents.
The ideal candidate will provide engineering and planning services supporting PD&E studies.
Essential Tasks
* Reviewing development plans for transportation system effects, infrastructure requirements, or compliance with applicable transportation regulations
* Documenting existing conditions and performing, analyzing, and summarizing research
* Working with our roadway design group to develop conceptual alternatives and design ideas for new or improved transportation infrastructure, such as interchanges, intersection improvements, pedestrian projects, and multi-modal facilities
* Collaborating with a team to complete feasibility studies, Efficient Transportation Decision Making documentation, PD&E studies, and other technical materials
* Performing QA/QC reviews to ensure completeness, accuracy, and conformity to engineering standards and practices
* Assisting in the pursuit of PD&E projects and other business development activities
* Assisting in the development of meeting materials, set up and break down of meetings, attendance, and facilitation
* Coordinating community review and public involvement activities for PD&E projects
* Identifying and coordinating with key stakeholders, special populations, and the general public
* Coordinating activities across multiple disciplines, both in-house and externally
Preferred Qualifications
* Bachelor’s degree in civil engineering, urban planning, economics, environmental or social science, geography, or a related field
* Ability to obtain a PE license or ACIP certification in the state of Florida once qualified.
* Three or more years of prior practical experience working on PD&E and transportation planning projects
* Familiarity with NEPA and Florida PD&E project requirements
* Proficiency with Microsoft Office
* Ability to communicate technical and complex information and to work well with others
* Possess attention to detail, organizational skills, and a positive attitude
* Ability to work independently
* Ability to multi-task and apply critical thinking skills
* Ability to work outside of regular business hours as needed (in case of public meetings or pop-up events)
* Ability to represent the client in a professional manner and maintain composure in tense environments
* Experience working in customer service is a bonus
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further informatio...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: Not Specified
Posted: 2025-09-06 08:14:39
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General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
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Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-09-05 08:51:40
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General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
....Read more...
Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-09-05 08:51:38
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Juris Concept est à la recherche d'un gestionnaire de compte.
Cette opportunité excitante vous permettra d'établir des liens avec une clientèle de bureaux d'avocats, apprendre de nouveaux domaines d'affaires et offrir des produits à la fine pointe de la technologie.
En tant que Gestionnaire de compte, vous ferez partie d'une entreprise solide et reconnue.
Le titulaire identifiera les besoins du client, démontrera les avantages du logiciel et présentera le portefeuille de solutions informatiques Juris Concept aux bureaux d'avocats et entreprises gouvernementales, augmentant ainsi la clientèle sur leur territoire et améliorant les relations avec les clients existants.
Le candidat idéal est un curieux, entreprenant et désireux de trouver la meilleure solution pour répondre aux besoins de nos clients.
Ce que nous recherchons
Nous recherchons un professionnel polyvalent et bilingue qui aime à la fois le côté humain et le côté bâtiment des ventes.
Nous recherchons également quelqu'un qui a :
* Une feuille de route éprouvée en matière d'atteinte et de dépassement de quotas.
* Expérience dans la vente de solutions logicielles SaaS ou B2B.
* Curiosité, dynamisme et aisance démontrés de travailler dans des environnements moins structurés.
* Capacité à créer et à gérer un pipeline de ventes avec discipline et responsabilité.
* Familiarité avec Office 365 et les outils CRM comme HubSpot.
Les responsabilités du poste:
* Participer à l'élaboration et l'exécution du plan de vente et de marketing du territoire ;
* Commercialiser et vendre de manière proactive la suite de solutions et de services Juris Concept;
* Présenter des démonstrations logicielles;
* Coordonner les négociations contractuelles;
* Planifier et exécuter des activités et des événements de prospection ciblés pour générer des prospects;
* Assurer la qualité et la rapidité des réponses aux appels d'offres;
* Enregistrer les informations et les progrès des clients dans le CRM des ventes;
* Maintenir un pipeline de ventes pour s'assurer que les objectifs de ventes soient atteints de manière cohérente et durable;
* Participer activement aux conférences nationales et régionales ainsi qu'aux réunions des groupes d'utilisateurs;
* Mener des affaires avec un niveau d'éthique exceptionnel;
* Établir des relations avec les pairs et les clients;
* Suivi avec le client après la vente pour assurer la satisfaction du client.
Points bonus si:
* Expérience dans la vente à des cabinets de services professionnels (juridiques, financiers, etc.).
* Être à l'aise avec les outils d'administration CRM ou d'aide à la vente.
* 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.
Nous avons des collègues, des clients et des par...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-09-05 08:39:18
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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!
Functions, Duties, Tasks:
These responsibilities are not intended to be all-inclusive:
* Scheduling, preparing, conducting and reporting Global Quality audits and assessments of commercial operations, both internally and externally (contracted) to assess the level of compliance with company standards, policies, practices and procedures and current regulations and guidelines.
* Participate in mock-inspections, as appropriate.
* Support training mentoring and qualification of new auditors to the team.
Participate in or lead the risk assessment of commercial operations. Integrate the information obtained through auditing and risk assessment and influence actions within and across EGQCA and the business areas involved/impacted.
* Drive the escalation of any compliance issues or significant risks identified during audits or when conducting risk assessment.
* Meet the requirements outlined in quality standards, quality manuals, policies, procedures, and tools.
* Participate in or lead the preparation of organizational metrics and trending of audit findings, when required.
* Influence internal and external customers and partners when improvement needs are identified.
* Maintain good interpersonal and communication skills with auditees and business areas with particular emphasis on verbal and technical writing skills.
* Be continually aware of current industry trends and regulatory agency interpretation of requirements for Animal Health.
* Participate or lead improvement efforts, including Six Sigma projects.
* Lead in the assessment of Top 7 product supply chain audits to support uninterrupted product supply.
* Represent EGQCA in conducting Due Diligent audits to support the business in new acquisitions.
Minimum Qualification (education, experience and/or training, required certifications):
* Ability to analyze detailed technical scientific information, while understanding the bigger picture. The auditor should be able to clearly identify and assess risk and impact associated with specif...
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Type: Permanent Location: Monheim, DE-NW
Salary / Rate: Not Specified
Posted: 2025-09-05 08:39:00
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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: R&D and Regulatory Intern
As an R&D and Regulatory Intern, you will be executing a project that impacts Elanco’s regulatory, clinical development, or innovation processes.
In this role you will directly enable Elanco to deliver products to our customers in ways such as identifying regulatory pathways to approval, improving internal data management systems, evaluating the competitive landscape, or assessing clinical efficacy models.
Your Responsibilities:
* Managing regular check-ins and reporting/presenting work to your direct supervisor
* Managing data in accordance with project deliverables
* Providing recommendations on process improvements or competitive landscape
* Working within cross-functional teams to implement project outcomes
* Some roles may include hands-on animal experience
What You Need to Succeed (minimum qualifications):
* Education: Currently enrolled in a field such as animal science, veterinary medicine (pre-vet or DVM), chemistry, biology, biochemistry, chemical engineering, pharmaceutical science, molecular biology or other related fields
* Degree: This role is open to students pursuing a Bachelors, Masters, PhD, or professional degree (e.g., DVM, MBA, PharmD, etc.)
* Microsoft PowerPoint and Excel experience
* Highly self-motivated, demonstrated learning agility, and critical thinking
What will give you a competitive edge (preferred qualifications):
* Experience working with statistical software or data management tools, proficient in Microsoft Excel
* Innovation and ideation mindset
* Hands-on experience with companion or farm animals and/or veterinary clinics
* Ability to work exceptionally well independently and with minimal supervision
* Have an interest in wanting to make a difference for pets, sustainability, veterinary medicine, or data-driven approaches
* Strong communication, interpersonal skills, speaking, and presentation skills
* Ability to make ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-09-05 08:39:00
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At CF&I Steel, L.P., our strength starts with our people! As a team we collaborate to solve problems, contribute ideas and challenge each other to ensure growth and ultimately success for the business and our employees.
Job Description and Responsibilities
As a Quality Systems Coordinator, you will maintain the Quality Assurance System including, but not limited to, recording and updating daily quality assurance and ISO 9001-2015, maintaining claim log, customer database, test report database, scheduling and training records, and job manuals, including all administrative functions.
Additional responsibilities include:
* Internal and external process and product audits
* Maintaining the SOPs which includes contacting/training the workforce when changes are made
* Management of the calibration system, issuing and recording process deviations
* Initiating, following and distributing Trials and their results
* Reporting daily and monthly Quality Index information
* Helping to communicate information associated with product quality and improvements to the workforce
* Helping with the daily management and maintenance of the quality system which can include assignments that may require off-hour or weekend work
* Maintaining scrap recipes, evaluating performance changes, reason, and auditing of charges
Requirements
* Bachelors of Science Degree or equivalent experience; Metallurgy/Materials Engineering, Chemical Engineering or Mechanical Engineering preferred
* Proficient in Microsoft Office - Word and Excel
* Proven written and verbal communication skills, including Quality Manual and Second-Tier Procedure Writing skills
* Excellent planning, time management, and organizational skills
* Strong problem-solving and proven decision-making skills
* Understanding of Steel mill processes: Rail, Rod & Bar, Seamless, Steel-making
* Initiative to identify areas, propose and initiate solutions
* Experience in the management of 6S projects
* Two years of Quality Assurance experience, preferred
* Familiar with Quality Management systems, preferred
* Certified Quality Auditor, preferred
* Experience in ISO 9001/Quality Systems, preferred
#TAS
COMPENSATION
* $80,000 – $87,000
Open & Closing Dates: 09/4/2025 – 10/30/2025
Our total compensation package includes amazing benefits!
* Competitive wages and bonus opportunities
* Family medical, dental, and prescription coverage at minimal employee cost
* Short and long term disability programs
* Competitive retirement plans
* Flexible Spending and Health Savings Accounts
* Employer-provided and Voluntary Life Insurance options
* Paid vacation and recognized statutory holidays
* Apprenticeship and career advancement within the company
* Tuition reimbursement
* Wellness program
All applicants must be eligible to work in the USA.
While we thank all thos...
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Type: Permanent Location: Pueblo, US-CO
Salary / Rate: Not Specified
Posted: 2025-09-05 08:38:57
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Accounts Receivable Analyst (12 Months Contract) - (Global Business Services)
Job Description
Accounts Receivable Analyst - (12 months contract) (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 in handling daily processing of sales and remittance advice data, and ensure timeliness and accurate processing 3rd Party & Intercompany within the agreed country SLA
* Management of data in strict adherence to internal control procedures are critical to effective credit control and collection of debts.
* Function as the expert on Cash Application processes and related systems.
Collaborate with work streams during process enhancements, acquisitions/divestitures, and major system implementations.
* Ensure that functional issues are appropriately prioritized and resolved.
* The incumbent is required to frequent liaising with internal sales and administrative personnel and customers to identify and resolve customer account issues.
* Engage actively with the business team country supported
* Initiate monthly engagement meeting as pulse check on the service delivery regular basis
* Reporting –KPI –Monthly basis
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 ...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-09-05 08:36:06
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Face à la Méditerranée, sur la légendaire Croisette, le Carlton Beach Club incarne l’élégance balnéaire été comme hiver, dans un esprit résolument chic et décontracté,
Nous recherchons notre Directeur/Directrice du Carlton Beach Club, un(e) chef d’orchestre passionné(e) et visionnaire, capable de faire rayonner cette adresse mythique auprès d’une clientèle locale et internationale.
Les principaux objectifs du poste :
Sous l’autorité de notre Directeur de la Restauration, vous déployiez les orientations définies et dirigez le fonctionnement des différents points de vente du Carlton Beach Club : le Restaurant de la Plage, le Beach Bar, notre Page Balnéaire ainsi que la Cuisine de la plage, en veillant à l’exécution d’un service de haute qualité et au maintien de standards d’un niveau irréprochable.
Vos missions seront les suivantes :
* Créer l’expérience – Transformer chaque visite en moment d’exception, en incarnant l’hospitalité du Carlton Cannes.
* Inspirer et guider – Fédérer, former et élever votre équipe pour atteindre l’excellence au quotidien.
* Piloter et innover – Développer les performances économiques tout en proposant de nouvelles expériences.
* Sublimer l’offre – Collaborer avec nos chefs et mixologues pour offrir une gastronomie raffinée et créative.
* Rayonner – Faire du Carlton Beach Club un incontournable de la Croisette, pour les Cannois comme pour les voyageurs du monde entier.
Ce que nous attendons de vous :
Pour remplir ce rôle avec succès, vous devez posséder les qualifications, l'attitude, les comportements, les compétences et les valeurs suivantes :
* Leader inspirant, avec une solide expérience (5 à 7 ans minimum) dans la direction d’un établissement haut de gamme (plage privée, restaurant, hôtel 5
*).
* Passionné(e) par l’art de recevoir, attentif(ve) au moindre détail.
* Capacité à performer dans un environnement saisonnier, exigeant et stimulant.
* Français et anglais courants (toute langue additionnelle est un atout).
* Créatif(ve), ambitieux(se) et déterminé(e) à faire rayonner un lieu iconique.
Ce que nous offrons :
* Poste à pourvoir en CDI – date de prise de poste à définir.
* Un package attractif (salaire attractif sur 13 mois + primes).
* L’opportunité d’écrire un nouveau chapitre de l’histoire du Carlton Cannes.
* Un cadre de travail exceptionnel, entre ciel et mer.
* La possibilité de créer, d’innover et de laisser votre empreinte sur une adresse légendaire.
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Type: Permanent Location: CANNES, FR-PAC
Salary / Rate: Not Specified
Posted: 2025-09-05 08:34:48
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What will your job look like?
The Manager, Safety and Training is responsible for implementing safety and training programs as defined by the Leadership of Safety Administration and will ensure compliance with State and Federal regulations, as well as corporate, client guidelines and policies.
This position is contingent on the award of contract.
Location: Okaloosa County, FL
What you’ll do:
* Manage a consistent safety culture that incorporates various departments, such as operations, safety and maintenance
* Oversee Corporate Safety Incentives and programs effectively and consistently, including assignment of Safety Points
* Implement and support the company and client’s safety management system (SMS) safety plan and initiatives Manage and monitor the FTA’s drug and alcohol DAMIS reporting requirements
* Monitor and support all location insurance claims activities to ensure effective communication with claimants, to help control claims costs and support claims closure
* Lead and support the local safety committee and SMS Ambassador group
* Oversees the locations worker compensation program to ensure compliance and effectively reduce/eliminate claims
* Deliver proper classroom, behind the wheel and mobility management training in accordance with contractual and company requirements
* Promote employee self-responsibility to achieve all safety goals and training requirements
* Ensures all new hires meet minimum qualifications for each division including, background and DMV checks
* Ensure all safety manuals, programs and policies and practices are current and meet the needs of the operating divisions; updating as appropriate
* Successfully complete all related audits including those conducted by the Company, the Client, internal staff members, and state and federal regulatory agencies
* Review, determine and respond to all vehicular, passenger and employee accidents/incidents, indicating the cause and preventability, identifying potential trends to be addressed in future training efforts
* Provide functional expertise in safety regarding hiring of safety department employees
* Collaborate with local Leadership to deliver comprehensive safety meetings and plans
* Act as the location drug program manager, ensuring compliance of FTA/DOT regulations
What you’ll need:
Experience, Education & Certifications:
* High School Diploma or G.E.D.
* Bachelor’s Degree (or equivalent combination of education and experience) in a related field
* 3+ years of relevant experience within the past 5 years, with increasingly responsible management responsibilities, with a similar scope, size, and complexity as this location (paratransit/fixed transit- 50+ driver-size)
* Previous management experience in a union environment
* Thorough knowledge of all applicable safety rules, regulations – ADA, FTA and DOT to include all corporate programs
* M...
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Type: Permanent Location: Panama City, US-FL
Salary / Rate: Not Specified
Posted: 2025-09-05 08:32:32
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ABOUT US
For more than 80 years, Baltimore Aircoil Company (BAC) has been leading the HVAC, Industrial and Refrigeration industries in developing and implementing customized cooling solutions that not only provide substantial energy savings for customers but conserve the most precious resources on the planet.
Wherever people live, work, play or learn, Baltimore Aircoil Company is there.
BAC makes custom-specific evaporative cooling solutions to maximize energy efficiency for HVAC, Industrial, and Refrigeration marketplaces.
POSITION PURPOSE
Are you ready to accelerate your career and become a future leader in operations?
The BAC Operations Leadership Development (B.O.L.D.) Program is a highly selective, customized, two-year rotational program designed to build a pipeline of high-potential operations leaders.
Through immersive rotational assignments, structured leadership training, and mentorship, participants gain the skills and experience needed to drive operational excellence across a global manufacturing organization.
B.O.L.D.
fellows will gain end-to-end operational leadership experience, work alongside senior leaders, and accelerate your professional development in a dynamic and growing organization.
If you’re ready to step outside your comfort zone, embrace new challenges, and make a lasting impact, B.O.L.D.
is for you.
PROGRAM HIGHLIGHTS
* Rotational Experience at BAC Manufacturing Sites: Complete multiple assignments across a variety of functions including manufacturing, supply chain, quality, engineering, and continuous improvement, gaining broad exposure to our operations.
Rotations could be in any of BAC’s current domestic locations.
Customized Development: Your rotation path will be tailored based on your experience, career goals, and business needs.
* Leadership Training: Engage in structured leadership workshops, technical training, and classroom learning using our 70-20-10 development model.
* Executive Mentorship: Receive direct guidance from program sponsors, senior leaders, and dedicated mentors.
* High-Impact Projects: Lead or support initiatives that drive operational innovation and deliver measurable business results.
* Cohort Experience: Collaborate and network with a select group of peers, building strong cross-functional and cross-site relationships
CANDIDATE PROFILE
We’re looking for ambitious, growth-oriented professionals who are passionate about building a career in operations leadership.
Ideal candidates will demonstrate:
* A bachelor’s degree (required) or equivalent experience.
* At least two years of professional work experience (operations or manufacturing experience preferred).
* Eligible to work in the US
* Commitment to two-year rotational program.
* Strong analytical, problem-solving, and leadership skills.
* Flexibility and willingness to relocate for rotational assignments as needed.
* A growth mindset, curiosity, and ability t...
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Type: Permanent Location: Dayton, US-TN
Salary / Rate: Not Specified
Posted: 2025-09-05 08:28:50
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America, Washington, District of Columbia, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Field Clinical Specialist is a visible position that will provide case support to physicians within certain territories. Case support will be done on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) ® technology.
The Field Clinical Specialist will also play a critical role in clinical studies including device training, case support and ensuring timely data collection for clinical programs. Case support may be required to support other territories at certain times.
Essential Job Functions
* Physician and hospital staff training, and procedural case coverage to ensure the safe and effective use of medical devices.
* Effectively meet the needs of internal and external customers with a sense of urgency and drive.
* Present clinical study training materials based on investigational plans to support the safe and effective use of medical devices, inclining stu...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-05 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:
Medical Affairs Group
Job Sub Function:
Medical Writing
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for an Associate Director, MSL Communications – US Medical Affairs (Hematology) located in Horsham, PA.
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
The Associate Director is involved in the development and execution of MSL Communications Strategy and digital medical education initiatives for the multiple myeloma portfolio for J&J.
Key Responsibilities:
* Lead development and maintenance of medical communication materials for Hematology Medical Science Liaisons (MSLs) and digital medical education platforms.
* Understand the remit of proactive and reactive materials including those for congresses, publications, disease state awareness, prescribing information, and any other educational topics that materials are needed to address.
* Liaise with partners to understand MSL and HCP educational needs and provide solutions within compliance and regulatory confines.
* Develop and maintain effective working relationships with internal partners (e.g., MSL team members, Medical Directors, Medical Excellence, Medical Communications) to fully understand the strategic needs and identify how the MSL Comm team can meet such needs through development of specific MSL tools and digital education resources.
* Project management of communication materials (e.g., track prioritization, timelines and progress).
Use the Veeva system for review and storage of all materials.
* Support slide creation and formatting from abstracts/posters/oral presentation from medical congresses and other clinical/scientific meetings for development of post-congress decks to be delivered to MSLs and other partners.
* Be responsible for quality control to ensure scientific accuracy of MSL and digital content and facilitate the review and approval process.
* Keep abreast of innovations and novel f...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-05 08:22:33
