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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 and commercial manufacturing 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 QC Chemist to join our Quality Control team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required.
Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance.
Responsible for timely analytical data reporting based on project timelines.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Demonstrate a more advanced knowledge of various test methods and instrument analysis techniques and be proficient with all sample types and test methods.
Perform more advanced troubleshooting/maintenance of the instrumentation.
* Responsible for more complex physical and chemical testing of raw material, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols.
* Demonstrate proficient ability to operate the instrument software applications, set up advanced sequences, troubleshoot software and report data while executing the higher complexity test methods that utilize instruments such as UV, FTIR, GC, and HPLC, and IC.
* As required, perform swabbing and analysis of more complex manufacturing equipment with no supervision in accordance with cGMP guidelines.
Provide input on cleaning related issues and investigations.
* Evaluate and maintain assigned calibrations for equipment in the laboratory as required and review the required documentation for compliance.
Review instrument qualification documents to support system change control actions and assist vendors during installation and PM’s.
* Investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines.
* Assist Management with writing and completion of in...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-07-30 08:56:40
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L’hôtel Carlton Cannes, a Regent Hotel, a rouvert le 13 mars 2023, suite à son magnifique projet de rénovation et d’extension.
L’hôtel est entièrement rénové et dispose de deux ailes prolongées dévoilant de nouvelles suites, d’un jardin intérieur de 2000m² agrémenté d’un bar et d’une piscine à débordement, d’un fitness & spa et d’un centre de conférence de 1800m².
Notre Maison est à la recherche de son/sa Réceptionniste de nuit en CDI.
Un accueil de luxe est primordial pour l’image de notre établissement.
Il implique un accueil élégant, chaleureux et personnalisé.
MISSIONS PRINCIPALES
Vos missions seront les suivantes, sans qu’elles soient totalement exhaustives :
* Vous êtes l’interlocuteur/interlocutrice privilégié(e) des clients de notre hôtel et assurez leur accueil, leur check-in tardifs, leur accompagnement en chambre et le suivi de leur satisfaction tout au long de leur séjour.
* Vous avez la responsabilité de gérer votre caisse et d'effectuer la facturation de nos clients lors des check-out tardifs.
* Vous participez à la clôture des opérations de comptabilité du jour pour la réception.
* Vous véhiculez l’image de notre hôtel par votre attitude, votre accueil chaleureux, votre professionnalisme et votre sens de l’hospitalité naturel.
QUALIFICATIONS
Vous avez de l'ambition, du talent et, bien entendu, certaines compétences indispensables ?
Pour remplir ce rôle avec succès, vous devez posséder idéalement les qualifications, l'attitude, les comportements, les compétences et les valeurs suivantes :
* Vous détenez une expérience professionnelle de 2 années minimum au poste de Réceptionniste dans un établissement haut de gamme
* Vous maîtrisez parfaitement la langue anglaise et le français; la maîtrise d’une troisième langue étrangère est un atout
* Vous maîtrisez le logiciel informatique Opera
* Vous possédez une grande clarté d’expression : vous devrez vous exprimer avec aisance, savoir vous montrer cordial(e), accueillant(e) et accessible
* Vous êtes familier(ière) du travail de nuit
* Vous détenez les qualités suivantes : autonomie, esprit d’équipe, réactivité, honnêteté, rigueur, méthode
* Vous aimez évoluer dans un contexte exigeant et en pleine évolution
* Vous appréciez particulièrement vous mettre au service de vos clients
* Vous devez répondre aux exigences légales pour travailler en France
AVANTAGES
En retour, nous vous offrirons un salaire et des avantages sociaux compétitifs, des réductions sur les hôtels dans le monde entier et des opportunités d'acquérir de nouvelles compétences et de faire progresser votre carrière.
* Poste en CDI, statut employé, à pourvoir dès que possible
* Salaire brut de 2571,87 euros + 18% de prime de nuit
* 13ème mois
* 35 heures hebdomadaires et 2 jours de repos consécutifs - ce poste implique...
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Type: Permanent Location: CANNES, FR-06
Salary / Rate: Not Specified
Posted: 2025-07-30 08:55:44
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Marketing
Job Sub Function:
Events
Job Category:
Professional
All Job Posting Locations:
Shanghai, China
Job Description:
Lead on BU FD sales analysis work including incentive management and reporting system.
Take responsibilities for support on key processes such as forecast planning and assiting production management.
Meanwhile drive FD effectiveness & efficiency via different projects and identify internal process excellence.
Responsibilities:
* Timely evaluate weekly performance via different reports and analysis
* Be in charge of incentive and Award Management
* Data system management via coordination with Digital & SC
* Routine demand planning support, including BO monitoring and allocation
* Provide support on SC management including rebate calculation and contract review etc.
* Improve business effectiveness & efficiency by internal process improvement opportunities
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-07-30 08:51:08
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
New Brunswick, New Jersey, United States of America
Job Description:
Global Finance Data Science Team at J&J is recruiting for a Senior Data Scientist. This position is located in New Brunswick, NJ.
As a Senior Data Scientist in Global Finance Data Science Team, you will be responsible for delivering data science production processes to a high standard, contributing to products that are consumed and scrutinized by senior leadership.
You will work in a global team of Data Scientists, Data Engineers and Machine Learning Engineers to advance data science/AI roadmap for J&J’s Global Finance function.
You will help deliver value-added insights and analytics to our finance and business leaders, reduce manual workload through automation, and enhance user-experience.
Project focus area will also include Predictive Sales Forecasting as part of SAP Analytics Cloud reporting capability, taking it from PoC to Production-grade standards.
This includes aligning finance and business needs, input data validations from different source systems, data reconciliation/validations and work on other ongoing enhancements/ad-hoc requests from leadership etc.
You will help in data science projects across their lifecycle: Design/ proof-of-concept (PoC), development, data pipelines and engineering, deployment, adoption by end-users and ongoing enhancements.
The capabilities developed will include predictive financial forecasting, Gen AI, descriptive analytics, data visualization and decision support.
You will need to ensure that PoC’s are put into production-grade with correct amount of automation, data validations and systems/process integration.
This role will involve understanding the needs of business stakeholders and advocating the merits of data-driven analytics to provide viable solutions.
Major Duties & Responsibilities:
· Adopt a highly successful forecasting process and technologies to deliver a monthly sales financial forecast for consumption by senior leaders
· Assessing BI sources to understand the impact of future events on forecast accuracy, developing judgement on how to adjust forecasts.
· Adjust data engineering pipelines for large datasets from finance/ERP systems and automate data science processes.
· Iteratively improve the process and models to solv...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-30 08:51:06
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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:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
Issy-les-Moulineaux, France, Lyon, Rhone, France
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/
J&J MedTech, Commercial Quality department, is recruiting for a Spécialiste Qualité reporting to the Commercial Quality Supervisor and to be based in Issy-les-Moulineaux or Lyon (France).
The Spécialiste Qualité effectively partners and collaborates in delivering the future of healthcare and performs quality support duties including complaint handling, internal auditing, general quality compliance duties.
Provides support for special quality projects.
Principal Duties and Responsibilities
• Complaint handling, vigilance reporting and FSCA activities
• Assist in internal auditing
• Assist in maintaining local QM Systems
• Take part in project teams when needed
Education and / or Experience
• Universities/Bachelor degree or equivalent
• 2+ years’ experience in regulated healthcare industry
• Basic understanding of QM-Systems and local/European Medical Device regulations
Other Skills and Abilities
• Ability to work effectively with minimal supervision
• Must be able to handle multiple and competing priorities
• Must be proactive in assessing work load
• Experience with MS-Office based applications
• Experience with IT Tools and data management
• Strong organizational and planning skills needed
• Adapts to changing priorities
• Must be committed to teamwork
• Able to identify and resolve regulatory/compliance problems of diverse scope in consultation with supervisor
• Good verbal and written communication skills (French and English)
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-07-30 08:51:05
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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:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
* Contributes with the establishment and implementation of cost-effective, results-based, and professionally-managed programs and innovative initiatives for the accounting area, under direct supervision.
* Assists with less complex components of projects, programs, or processes for the accounting area in compliance with GAAP (Generally Accepted Accounting Principles) and applicable governance policies.
* Performs simple trend analysis to support continuous improvement efforts for the organization's accounting strategy.
* Participates in the completion of internal and external audit, and ad hoc requests.
* Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
Key Responsibilities:
* Responsible for implementing accounting and daily operations for Intercompany Accounting process area for sophisticated MRCs.
* Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements.
* Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope.
* Deep expertise, fully knowledgeable of the Worldwide Procedures and compliance requirements for respective areas.
* Regular focus on Balance Sheet reconciliations to minimize open items.
* On the job training for new team members / BPO partners.
* Support auditors and legal authorities with the execution of required activities.
* Understand, enforce, and implement per worldwide policies and procedures.
Identify compliance risks and recommend solutions.
* Ensure strong internal controls are in place, to achieve “adequate” internal and external audit ratings.
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-07-30 08:50:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Business Support
Job Sub Function:
Administration & Secretarial
Job Category:
Professional
All Job Posting Locations:
Latina, Italy
Job Description:
Job Description:
We are searching for the best talent for MSAT Assistant Scientist to be in Latina.
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
Purpose:
For the Italian production plant of Janssen (Borgo San Michele-Latina) we are looking for an ASSISTANT SCIENTIST to be hired with a TEMPORARY CONTRACT in the MSAT DEPARTMENT.
The person will be part of the team who manage MSAT LCM projects and will report to the MSAT Senior Manager (LCM).
As an MSAT Assistant Scientist, you will:
* As Project Leader ensure planning and coordination of the activities in collaboration with the various departments involved in the implementation of the projects.
* Proactively identify risks to define mitigation strategies.
* Assess the business impact, quality, compliance and safety involving stakeholders from other departments.
* Ensure compliance with the time of introduction, balancing the base business production needs.
* Ensure timely communication to MSAT Sr Manager and Global Functions to align with the production plans themselves.
* Ensure the timely availability of quality documentation for the project execution.
* Perform and/or support investigations for non-conformances in case of occurrence during project activities.
* Process Analytical Technologies, Multivariate Analysis & chemometrics application.
Qualifications:
* Experience in the pharmaceutical industry (Oral Solid production is preferred).
* Academic knowledge of lines, processes, materials and equipment for pharmaceutical process (oral solid pharma production competence is preferred).
* Fluent in English (B2 level and above).
* Good knowledge of quality, compliance and GMP related to manufacturing and packaging of pharmaceutical products.
* Basic experience in Project Management with ability to work in a multidepartment and dynamic e...
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Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-07-30 08:50:50
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for an Associate Scientist, Biotherapeutics Development & Supply Active Pharmaceutical Ingredient (API) to be onsite in Malvern, PA.
Purpose:
The Associate Scientist, Biotherapeutics Development & Supply Active Pharmaceutical Ingredient (API) will perform process development and manufacturing for large molecule cell culture processes.
You will be responsible for:
* Performing cell culture process operations covering vial thaw through bioreactor harvest
* Aseptic technique and cell culture manipulations involving a variety of cell culture vessels (i.e., shake flasks, and wave bioreactors)
* Large scale and single use bioreactors, including assembly, preparation, operation, and maintenance
* Clean In Place and Steam in Place procedures
* Record and analyze experimental data, verify data integrity and accuracy, and report/summarize findings to the project team
* Works closely with project teams and collaborate with support functions to meet or exceed the goals and objectives of Protein Therapeutics API Development – Biologics Therapeutics Development & Supply
* Thrive in a diverse team setting by giving technical expertise to multiple large molecule programs, proficient with documentation, and reviewing analytical data
* Maintain equipment logs and assist with the resolution of equipment downtime
* Follow laboratory safety procedures
Qualifications / Requirements:
Education:
* Minimum of a Bachelor’s degree is required
Required:
* Minimum 1 year of experience in the pharmaceutical and/or biotechnology industry
* Experience with upstream processing and purification of large molecules
* Experience maintaining written r...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-07-30 08:50:22
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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:
Athens, Georgia, United States of America
Job Description:
Johnson & Johnson is recruiting for an Environmental Health & Safety (EHS) Specialist located at the Athens, Georgia facility.
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
The EHS Specialist is to apply scientific, engineering and other technical skills to support site EHS activities to develop and coordinate documentation, training, communication, scheduling and oversight needed to maintain compliance with government regulations and Johnson & Johnson policies related to Industrial Hygiene, Chemical Substance management and related OHSA programs.
Provides focused technical expertise around health and safety standards, hazard assessment, accident investigations, and emergency responses to promote workplace safety!
Key Responsibilities:
* Leads all elements of plant Hazardous Communication programs including SDS management, Chemical Hygiene, Laboratory safety, Hearing Conservation, and Bloodborne Pathogen programs.
Works to ensure that Hazardous Communication information is maintained, to include Safety Data Sheets, Chemical Compatibility Charts, as well as Chemical risk assessments.
* Assist in preparing and submitting EHS regulatory agency applications, permits, and reports to ensure compliance with applicable regulatory standards.
* Provide support for Industrial Hygiene, Ergonomics, and other EHS programs.
Including execution of the annual Industrial Hygiene sampling plan and noise monitoring for the site.
* Perform respirator training and fit testing, assist with EHS training activities, and coordinate EHS training days.
* Participate in EHS program reviews, Assurance audit process, GEMBA walks, and various risk assessments.
* Schedule and conduct routine inspections of facilities, equipment, and operations to identify and evaluate risk factors, ultimately eliminating potential hazards and hazardous processes.
* Assist in the development and delivery of EHS programs, including employee safety...
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Type: Permanent Location: Athens, US-GA
Salary / Rate: Not Specified
Posted: 2025-07-30 08:50:06
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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:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson Innovative Medicine is hiring a Senior Scientist, Biostatistics to be located in either Raritan, NJ, Titusville, NJ, Spring House, PA, or San Diego, CA.
The Senior Scientist, Biostatistics will support the Oncology Therapeutic Area with a focus on: solid tumors or hematologic malignancies; cancer interception with the goal of developing products that interrupt the carcinogenic process; biomarkers that may help guide targeted, individualized use of our therapies; as well as safe and effective identification and treatment of early changes in the tumor microenvironment.
Key Responsibilities:
* Provide statistical input into the clinical development of drugs for treatment of cancer.
* Work with the clinical team in designing clinical studies, leading/authoring the statistical analysis plan, conducting the statistical analysis, and providing statistical input to the clinical study report.
* Provide input in the preparation of scientific presentations and manuscripts.
* Participate in process improvement, training, standards development and enhancing statistical technical expertise.
* Liaise with other statisticians within the organization, building working relationships with therapeutic area leaders, internal SAS programmers, clinical trial managers, and personnel from regulatory affairs, medical writing, and other disciplines as needed.
Qualifications
Education:
A Ph D in Statistics or related field, OR a Master’s Degree with at least six (6) years of clinical data analysis experience, is required.
Experience and Skills Required:
* Working knowledge of statistical softwa...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-30 08:49:59
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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:
Business Process Quality
Job Category:
People Leader
All Job Posting Locations:
San Angelo, Texas, United States of America
Job Description:
Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Process Quality Specialist to be located in San Angelo, TX.
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/ (https://www.jnj.com/
Under the direction of the Business Unit Manager and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position
• Leads investigations and rapid response teams (RRT) of the negative trends, quality/product process investigations & product complaints.
• Provides technical leadership towards the identification of the causes for non-conformances & process' failures, and implementation of the immediate, corrective & preventive actions.
• Reviews & analyses quality trends with the manufacturing team & provides guidance for process enhancement setting work priorities, effective in-depth investigation.
• Provides training and education to the manufacturing team on tools for process evaluation and enhancement.
• Provides guidance to manufacturing supervisors or support groups to ensure that effective in-depth investigations are performed.
• Manages all preparation and execution for internal and external audits including audit observations and implementation of corrective actions.
• Analysis of data and based on the trends recommends actions for process, equipment and system improvement.
• Writes procedures, protocols and any other Documentation needed for the enhancement of processes and systems.
• Provides training and education to the manufacturing team on tools for process evaluation and enhancement.
(Analytical trouble shooting, FMEA, statistical concept application and QS...
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Type: Permanent Location: San Angelo, US-TX
Salary / Rate: Not Specified
Posted: 2025-07-30 08:49:57
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Marketing
Job Sub Function:
Strategic Marketing
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
Johnson & Johnson MedTech – Neurovascular division is currently seeking a Marketing Manager, GSM. This is a hybrid role based in Irvine, California.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech/
Key Responsibilities:
· Identify appropriate sources of market intelligence and apply analytics to make clear, data-based decisions
· Interface with physicians and broad international customer base to identify market trends and unmet clinical needs for the treatment of neurovascular disease
· Translate customer needs into product design requirements to develop differentiated product concepts
· Closely collaborate with R&D to provide customer insights during the product development cycle
· Build collaboration with cross-functional partners including regulatory, clinical affairs, professional and commercial education, supply chain and sales team to ensure seamless product commercial readiness
· Collaborate with global marketing partners to communicate product portfolio updates, understand local customer needs and coordinate product launches
· Identify appropriate market opportunities through synthesis of sound segmentation, targeting and positioning strategies and sales collateral
Qualifications:
Education:
· Bachelor’s degree required
· MBA or equivalent strongly preferred
Experience and Skills:
Required:
· Three years of marketing or related experience with at least two years of marketing experience in the medical device sector
· Ability to construct global marke...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-30 08:49:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Professional
All Job Posting Locations:
São Paulo, Brazil
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at: https://www.jnj.com/innovative-medicine
We are searching for the best talents for these 4 positions of Senior Site Manager (home based).
Purpose: A Senior, Site Manager is a mid-level site management role with typically 3-5 years of experience.
This role serves as the primary contact point between the Sponsor and the Investigational Site.
A Senior, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
Responsibilities may include assisting with site selection, site qualification assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.
The Senior, Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial Delivery Leader) to ensure overall site management while performing trial related activities for assigned protocols.
A Senior, Site Manager may contribute to process improvement, training and mentoring of other Site Managers.
A Senior, Site Manager is generally expected to be able to operate independently with little or limited supervision.
Principal Responsibilities:
1 Acts as primary local company contact for assigned sites for specific trials.
2 Actively May participate in site feasibility and/or Site Qualification Visit.
3 Attends/participates in investigator meetings as needed, may be expected to help prepare meeting materials and may be required to present at the IM.
4 Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to...
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Type: Permanent Location: São Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-07-30 08:49:55
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Roche in 50 Worten:
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein. Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Was macht unseren Bereich aus:
Der Bereich Diagnostics Operations Penzberg (DOZ) ist weltweit der wichtigste Roche Diagnostics Produzent von qualitativ hochwertigen Einsatzstoffen bis hin zu speziellen Kits.
Du startest bei uns im Bereich Diagnostics Operations Penzberg in der Abteilung Qualitätskontrolle.
Hier werden Roh- und Einsatzstoffe für die gesamte diagnostische Produktion untersucht und freigegeben.
In der instrumentellen Analytik erwartet Dich ein interessantes Methodenportfolio aus chemischen und biochemischen Analysemethoden mit den Schwerpunkten HPLC (High-Performance Liquid Chromatography)- und GC (Gas Chromatography)- sowie MS (Massenspektrometrie)-basierter Analytik.
Das Team:
Wir sind ein 17-köpfiges Team, bestehend aus Laborant/innen, Laborassistent/innen und einem Laborleiter.
Unterstützt werden wir durch 2 Expert/innen.
Unsere vielfältigen und abwechslungsreichen Aufgaben im Rahmen der Freigabeanalytik gehen wir gemeinsam mit Spaß und Engagement an.
Hierbei freuen wir uns auf tatkräftige Unterstützung mit Dir als aufgeschlossenes und motiviertes Teammitglied, das uns mit seiner Leidenschaft und seinem langjährigem Know-how der instrumentellen Analytik aktiv verstärkt.
Gerne übertragen wir Dir folgende Aufgaben:
Deine Aufgabe umfasst die Analytik und Freigabe von qualitativ hochwertigen Roh- und Einsatzstoffen für die gesamte diagnostische Produktion:
* Du führst selbstständig Freigabeanalysen an Biochemika sowie Roh- und Einsatzstoffen unter Anwendung von HPLC- und GC- sowie MS-basierten Methoden sowie weiteren (bio)-chemischen und molekularbiologischen Testmethoden durch
* Darüber hinaus bist Du zuständig für die Bearbeitung von Mustern, Sonderanalysen und Spezialaufgaben wie Methodenvalidierung
* Dabei wertest Du die Analytik-Ergebnisse selbstständig aus und dokumentierst diese gemäß DIN ISO / GMP bzw.
geltenden Arbeitsanweisungen
* Du erkennst, dokumentierst und meldest Abweichungen und erstellst außerdem OOS- (out of specification) und Abweichungsberichte
* Die Pflege des Arbeitsplatzes sowie der verwendeten Geräte unter Einhaltung der Arbeitsvorschriften wie DIN/ISO und GMP gehört zu...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-07-30 08:46:41
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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
A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.
That’s what makes us Roche.
The Opportunity
The Genentech/Roche African Genomics Program invites applications for a highly motivated and team-oriented Scientific Program Manager.
The selected candidate will join the African Genomics Program to serve as both a scientific and overall project manager on multiple genomic collaborations to enable and accelerate novel research on the African continent and beyond.
* An understanding of genetic or multi-omic datasets is critical for this role, including understanding the use and analysis of whole-genome sequencing data.
Strong organizational and communication skills and experience managing complex projects are also required.
* In addition to managing scientific projects, the successful candidate will also be responsible for overseeing various operational activities including data flows and data transfers.
* The role is a key strategic partner that drives the successful execution of cross-functional initiatives, ensuring alignment with organizational goals and program roadmaps.
The role will facilitate collaboration across teams, manage complex program structures, and guarantee timely delivery of programs with quantifiable results.
Key Challenges
* Management and tracking of multiple interdependent projects with different collaborators and stakeholders.
* Management and organization of data flows including coordinating with people in the informatics, computational biology, software development, and information infrastructure space
* Ensure on-time program delivery by managing across related project timelines and workflows.
* Manage the overall portfolio of projects and health of the program - identifying risks and escalating issues as needed to ensure project success.
* Consistently communicate program plans, progress, risks, changes, and successes with clarity and objectivity. Drives a high degree of accountability across program teams and groups in order to meet objectives and foster effective collaboration.
* Responsible for the overall program budget.
* Liaise with teams working on global procurement, service agreements and local contracts, act as PPOC on AGP for these internal collaborators
* Awareness of ...
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Type: Permanent Location: Nairobi, KE-110
Salary / Rate: Not Specified
Posted: 2025-07-30 08:37:43
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Classification:
Non-Exempt
$15.98
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The Soil Counter/Sorter handles, counts, sorts and records incoming soiled textiles from the customer.
Identifies damaged or abused textiles.
Prepares and transfers textiles to other departments.
Performs other tasks as needed.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Open bag of soiled textiles, then sort them by type, size and color.
- Count textiles manually or electronically, and transfer them into sorting systems.
- Identify damaged or abused textiles and record into sorting systems.
- Meet efficiency and safety standards for the position.
- Follow instructions as directed by supervision.
Additional Functions:
- Work in other production positions as needed.
Qualifications:
- Recognize colors and sizes, count accurately.
- Comprehend and follow direction.
Typical Physical Activity:
- Physical Demands consist of standing, walking, reaching overhead, pushing, pulling, grasping, lifting up to 50 lbs.
and stooping.
- Physical Requirements consist of being able to meet the physical demands for the entire shift.
Typical Environmental Conditions:
- Production areas of a typical industrial laundry facility, which includes variations in temperature, odors, humidity, lint and dust.
Soiled linens come from a variety of customers such as restaurants, hotels, medical facilities and shops.
Travel Requirements:
- none.
Education:
- none.
For a general description of benefits that are being offered for this position, please visit alsco.com/benefits.
Alsco is an Affirmative Action/Equal Employment Opportunity Employer.
Revised: 04/29/2022
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal emp...
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Type: Permanent Location: Reno, US-NV
Salary / Rate: Not Specified
Posted: 2025-07-29 09:08:55
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Medisolution is seeking an Implementation and Support Consultant with a solid background in Financial processing and reporting within the Healthcare industry.
As an Implementation and Support Consultant, you will work closely with both clients and development team members to achieve client goals.
You will be the frontline point of contact providing high quality, friendly, and prompt technical support.
Responsibilities include overall project management, creation of project deliverables, implementation, client training, demonstration, program documentation, and product testing.
The ideal candidate must be a team player with strong people skills, self-learning skills, and share a dedication to the latest technologies and techniques.
To excel in this role, you’ll need to have an analytical mind and a passion for digging into the details to find unique solutions to complex problems.
You’ll need to be able to leverage your natural curiosity to help you thrive in ambiguity and tackle problems.
What your impact will be:
* Provide high quality support to our clients, ensure we are meeting contractual obligations and maintaining a high level of customer satisfaction and timeliness of resolution;
* Communicate to clients when there are changes to the application, and occasionally regulatory and legislative updates;
* Implement new customers from start to finish including but not limited to analyzing set up needs, testing, training;
* Provide ongoing customer support including; troubleshooting issues, providing application training to new staff, including reporting training on an Excel-based application;
* Prepare and keep up to date training documentation and update user guides when needed;
* Assist with business development-related activities including the development of proposals, statements of work, and delivery of presentations;
* Participate in project planning and implementation;
* Develop a deep understanding of the functional / technical features of our applications and use this knowledge to address application-related issues and questions;
* Troubleshoot software and implementation issues and provide workaround and functional implementation guidance as needed, completing support cases for clients with a quick turnaround; via telephone, email, and/or ticketing system;
* Use ticketing system to review tickets, prioritize ticket queue, update and resolve tickets with complete and accurate documentation in a timely and effective manner;
* Diagnosing and documenting software issues / bugs, performing the appropriate resolution; working with other members of the technical support and software development teams in order to identify and resolve problems in a timely, efficient, and effective manner;
* Design of new product features alongside members of the software development team;
* Perform other duties as required or assigned.
What we are looking for:
* CPA (Chartered Prof...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-07-29 08:51:32
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Chez PG Solutions, notre équipe de Croissance et Innovation relevant de la R&D regroupe plusieurs chefs de produits passionnés qui travaillent à transformer les solutions numériques destinées au secteur public.
Nous sommes actuellement à la recherche d’un Gestionnaire de produit (Product Owner) pour piloter l’évolution de notre gamme de produits en évaluation foncière et géomatique, dans un contexte de refonte vers une plateforme web moderne.
Le Gestionnaire de produit joue un rôle central dans notre démarche d’innovation.
Il agit comme lien stratégique entre les clients, la direction, l’équipe des ventes et l’équipe de développement, afin de faire évoluer le produit en réponse aux besoins du marché, aux tendances technologiques et aux exigences réglementaires.
Joueur clé au sein d’une équipe multidisciplinaire, la personne recherchée doit faire preuve de rigueur, d’autonomie et d’un excellent sens de la collaboration.
Elle est responsable de maintenir une vision claire du produit, de bâtir un plan d’évolution cohérent, et de mobiliser les parties prenantes autour de cette vision.
En collaboration avec l’équipe de développement, elle analyse les besoins des clients, propose des solutions concrètes, identifie les fonctionnalités clés et les communique de façon claire et structurée.
Profil recherché:
Nous sommes à la recherche d’une personne rigoureuse, curieuse et dotée d’un fort esprit de collaboration, possédant une bonne connaissance du domaine de l’évaluation foncière municipale au Québec, notamment en ce qui concerne le cadre réglementaire et les pratiques professionnelles en vigueur.
Une bonne compréhension des concepts et des outils en géomatique, tels que les systèmes d’information géographique (SIG), les données spatiales et la cartographie, constitue également un atout important.
Votre rôle:
* Actuellement, nous modernisons notre solution d’évaluation foncière en la faisant évoluer vers une plateforme web innovante, performante et conforme aux normes professionnelles du Québec.
Notre produit intègre également un important volet géomatique, essentiel à notre approche.
* En tant que Gestionnaire de produit, vous serez au cœur de la refonte de notre produit.
Vous piloterez la vision, la stratégie et l’évolution fonctionnelle de la solution, en collaboration avec les parties prenantes internes et externes.
Vous contribuerez à bâtir une plateforme web moderne, intuitive et conforme aux exigences réglementaires et aux meilleures pratiques du domaine.
Responsabilités:
* Compréhension du domaine et des utilisateurs
* Apprendre les systèmes, les processus de travail et les réalités opérationnelles de nos clients.
* Recueillir, analyser et documenter les besoins des utilisateurs, en clarifiant la portée des demandes.
* Représenter les utilisateurs et les parties prenantes auprès de l’équipe de développem...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-07-29 08:51:29
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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.
As a leader within Alcoa, you can help fulfill our purpose and realize our vision build a legacy of excellence for future generations.
Be part of the team that is helping shape a better workplace with opportunities that help everyone thrive and build diverse, rewarding careers.
You have the power to shape things and individuals to make them better.
About the Role
Alcoa is seeking a visionary and strategic leader to join our team as Regional Environmental Director in Perth, Australia.
This is a rare and exciting opportunity to shape the future of environmental stewardship across our Australian operations, while leveraging the capabilities of Alcoa’s world-class forest research centre and contributing to groundbreaking biodiversity initiatives.
This role is ideal for a seasoned environmental executive who is passionate about sustainability, innovation, and leadership.
You will be instrumental in driving Alcoa’s environmental agenda, aligning with our core values and global sustainability priorities, while ensuring compliance, mitigating risk, and enabling responsible growth across our Refining, Mining, and Smelting operations.
Key Responsibilities
As a strategic leader, you will:
* Set and lead the environmental strategy for Alcoa’s Australian operations, aligning with global sustainability goals and corporate values.
* Champion biodiversity innovation, collaborating with Alcoa’s forest research centre to develop and implement pioneering environmental solutions.
* Provide expert regulatory guidance across all Australian sites, ensuring compliance with State Agreements, the Environmental Protection Act 1986, and other relevant legislation.
* Partner with regional and site leadership to support growth and expansion initiatives, ensuring environmental integrity is maintained.
* Facilitate cross-functional collaboration to address regulatory changes, compliance trends, and continuous improvement opportunities.
* Lead and mentor a team of environmental professionals, fostering talent development and building a high-performing, future-ready team.
What’s on offer
* Attractive remuneration and variable bonus plan.
* Flexible hybrid working options available.
* Employee growth and development opportunities.
* Parental leave support for all caregivers.
* Paid employee volunteering hours within our community.
* Employee assistance program for personal support services.
* One additional paid Alcoa Flexi Day.
* Alcoa Live Well program offering travel, lifestyle, health and wellbeing discounts.
* Salary packaging for a novated car lease, employee share plan and superannuation options.
* Connect and be part of a community that celebrates diversity thr...
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Type: Permanent Location: West Perth, AU-WA
Salary / Rate: Not Specified
Posted: 2025-07-29 08:47:12
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Safety & Health Assistant Manager
Job Description
This Safety & Health Assistant Manager is responsible for developing, implementing, and overseeing safety and health programs within a tissue production facility, ensuring that all employees work in a safe environment in compliance with safety standards and regulations.
This role involves identifying potential risks, implementing preventive measures, and investigating incidents to drive continuous improvement.
The Safety and Health Manager will collaborate with various departments to promote a culture of safety and facilitate ongoing improvements.
1.
Provide professional advises and leadership to establish, maintain and promote the EHS management systems (ISO-14001& ISO-45001) to reduce or eliminate industrial accident, health hazards, environmental impact, asset loss and regulation violation.
2.
Be responsible for all safety & health projects and implementation, including both internal and external audits.
3.
Coordinate and communicate with both domestic and oversea units or mills.
Need to cooperate with foreign colleagues directly.
4.
Provide coherent, trusted and effective safety & health support to mill managers to meet / exceed their objectives.
Primary Location
Taiwan-Ta-Yuan
Additional Locations
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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Type: Permanent Location: Ta-Yuan, TW-TAO
Salary / Rate: Not Specified
Posted: 2025-07-29 08:46:20
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Senior Toxicologist
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
In this role, you will:
The incumbent Senior Toxicologist safety professional guides clinical substantiation and conducts human health safety assessments of cosmetic, consumer, personal care, and professional products primarily in the America regions.
The incumbent will conduct product safety and health risk assessments, ensuring compliance to safety standards and regulations, and collaborate on stewardship initiatives on a range products and components through all phases of development, commercialization and post-market surveillance.
Responsibilities include providing expert guidance on safe design to product development teams, development of safety testing strategies, human health risk assessment, and product safety guidance to enable and meet new product development milestones and ensure K-C products are safe for their intended use, support product registration as applicable, and comply with all applicable governmental safety rules, regulations, corporate standards and consumer expectations.
The incumbent will represent Product Safety and work closely with cross-functional partners in product development, clinical, medical affairs, legal, quality and regulatory affairs as well as external groups including subsidiaries, trade associations and governmental agencies to ensure product safety.
* Conduct and communicate human health safety risk assessments on a broad range of products, including the substantiation of safety-related claims and taking into consideration identified hazards and exposure according to the intended product use.
This includes assessment of scientific literature, evaluation of the toxicological database, determination of appropriate toxicological and other safety endpoints, design hazard analysis, failure mode analysis, exposure assessments, clinical evaluation and written documentation.
* Manage the design, monitoring and interpretation of chemical characterization analyses, in vitro and in vivo toxicology, safety testing, and biocompatibility conducted under Good Laboratory Practices (GLP), and when applicable, clinical studies conducted under Good Clinical Practices (GCP).
* Contribute to and effectively communicate product safety guidance and regulatory safety compliance information, safety point-of-view papers and health risk assessments to internal or external technical experts as well as functional and business unit leaders and management.
Represent K-C’s key business interests on trad...
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Type: Permanent Location: Irving, US-TX
Salary / Rate: Not Specified
Posted: 2025-07-29 08:45:58
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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:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
Accountant 1, Global Intercompany
“Reimagine the possibilities” at Johnson and Johnson Global Finance! We live this motto every day by creating game-changing business solutions for the world’s largest and most broadly-based healthcare company.
As a member of our Global Finance team, you will have exclusive access to a network of financial professionals located in over 60 countries.
This new network will help you build on your current skills and explore opportunities to grow your career in J&J.
Key Responsibilities:
Be compliant with applicable laws and regulations, and follow guidelines in the J&J Credo
Maintain Operational Excellence
* Responsible for executing accounting and daily operations for Intercompany Accounting process area.
* Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements.
* Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope.
* Deep expertise, fully knowledgeable of the Worldwide Procedures and compliance requirements for respective areas.
* Regular focus on Balance Sheet reconciliations to minimize open items.
* On the job training for new team members / BPO partners.
* Support auditors and legal authorities with the execution of required activities.
* Understand, adhere, and execute per worldwide policies and procedures.
Identify compliance risks and recommend solutions.
* Ensure strong internal controls are in place, in order to achieve “adequate” internal and external audit ratings.
Talent Management
* Recruit, Onboard and Training of new joiners.
Be a Trusted Business Partner
* Execute global Strategy & Solutions in line with taxonomy.
* Support Process Subject Matter Experts (SME's) and Operational Key Contacts (OKC's) to ensure cross sector, cross region, and cross process alignment, ensuring good documentation is maintained and consistency of a global approach.
Create Game-Changing Innovation
* Generate ideas, fosters, and implements continuous improvement mindset, identifying and pursuing proc...
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-07-29 08:33:33
-
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 – Primary Care Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Beijing, China
Job Description:
工作职责：
* 利用专业的电生理知识和技能，为术者提供手术支持，确保手术安全顺利进行；
* 熟悉客户手术习惯，与术者高效沟通，不断精进专业技能，在区域独立完成从简单到复杂的心律失常手术支持
* 紧跟行业和公司发展趋势，主动学习和掌握行业内新理念、新技术，新产品的优势和使用，能够制定针对性、可拆解的推广沟通方案
* 熟练使用新产品、数字化等新工具以及新技术，协助专业教育团队提升术者理念，技能和信心
* 有效传递新产品、新技术的价值，不断提升客户对于新技术的接受度，以安全高效的方式开展手术，服务病患
* 承担团队内教学带教工作，与团队共同进步，通过理论授课、模拟器练习、术中导管室带教、病历复盘等，有效提升新同事/初阶同事的知识和手术支持能力
* 严格遵守公司的合规政策，完成上级交予的其他任务
* 接受一定程度出差
能力要求：
* 具有自驱力，不断精进专业水平，积极学习业内不断发布涌现的新产品、新技术知识，并进行应用；
* 乐于沟通协作，与团队共同进步，共同承担团队目标，互相协助
* 有坚韧不拔的精神，遇到困难不轻易放弃，
* 有创新思维，积极探索方案并解决问题
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-07-29 08:33:13
-
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 D
Job Category:
Non-Standard
All Job Posting Locations:
Shanghai, China
Job Description:
* Support Site Record Coordinator to maintain the process of Document Control & Record Control under Ethicon Minhang Quality Management System.
支持工厂记录协调员进行爱惜康闵行质量管理系统下的文档控制和记录控制流程的维护。
* Support Site Record Manager for the execution of Record Management Program to ensure Record Management requirements and local procedures aligned to Franchise Record Management Policy and WWRIM Policy & associated standards.
协助工厂记录经理执行记录管理项目以确保记录管理要求和本地程序与事业部记录管理政策、WWRIM政策和相关标准保持一致。
* Maintain site document control and record control procedures to align with Franchise procedures, J&J Policy and regulation requirement.
维护工厂文档控制和记录控制程序以和事业部程序，强生政策和法规的要求保持一致。
* Update site internal document master list in a timely manner.及时更新工厂内部文档主清单
* Deliver the training of document Control & record control across whole plant.
对整个工厂进行文档控制和记录控制的培训
* Lead department record coordinators to implement site Record Management Program by executing the process of the archiving of Paper & Electronic records, control of Vital & Non-vital records, onsite record storage & offsite record storage.
组织部门记录协调员进行纸质和电子记录的归档、重要和非重要记录的控制、厂内和厂外记录保存流程以执行工厂记录管理项目。
* Take of Role of Quality Review Staff by following Product Release process for batch history record transfer and review activities.
依据产品放行程序负责质量审核人员的角色，以完成批生产历史记录的交接和审阅活动。
* Act as the backup of site training responsible and the site ComplianceWire Admin.
担任工厂培训人员的后援支持以及工厂ComplianceWire管理员。
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-07-29 08:33:13
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Human Resources
Job Sub Function:
Health Services
Job Category:
Professional
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Sr.
Occupational Health Nurse located in Titusville, NJ.
Established and productive individual contributor, who works under moderate supervision.
Services are provided under the mentorship or supervision of a Site Lead or Health Services & Resources Supervisor and general direction of the designated physician (as required by law).
Provides occupational health nursing, medical, and integrated services consistent with the policies, guidelines, objectives, and content of the Johnson & Johnson Occupational Health program.
Adheres to established privacy, safety, and confidentiality regulations.
Principal Responsibilities
* Provides nursing services and emergency (first-aid) treatments to employees who become ill or suffer an accident on company premises, arranging for transportation to another care provider, if needed.
Notifies all concerned.
* Collaborates cross-functionally to create and maintain safe work environments and facilities.
* Coordinates the investigation of complaints or problems and takes corrective action.
* Acts as a liaison with medical providers to ensure patient adherence to billing policies and procedures.
* Coaches more junior colleagues in techniques, processes, and responsibilities.
* Participates as an active member of the First Aid/Emergency Response Team.
* Under supervision of a physician, administers medications and performs various minor treatments or therapies for injured or ill employees.
Administers injections for allergies and for overseas travel as directed by the physician.
* Provides various preventive health evaluations and tests in accordance with the company Health Services program protocols.
* Conducts health profiles, health evaluations and other services within the integrated employee Health Services & Resources strategy including but not limited to health promotion education, health screenings, drug screenings.
* Complies with policy, procedures, standard of nursing practice, written standing orders, protocols and medical directives as required by the company and State Nurse Practice Act.
* Maintains accurate clinical records, utilizing approved medical, nursing, and statistical formats...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-29 08:33:12
