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PURPOSE AND SCOPE:
The Inpatient RN provides direct patient care in accordance to company policies and procedures which includes FMCNA compliance programs and contracted hospitals’ policies and procedures.
Areas of practice are diverse, including, but not limited to, hemodialysis, peritoneal dialysis, continuous renal replacement therapies, apheresis, and ultrafiltration.
The Inpatient RN will partner with the hospital to provide quality care to the patient and deliver care that provides a positive patient experience.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Under limited supervision, applies considerable knowledge to perform a broad range of tasks which include but are not limited to direct patient care in multiple modalities not limited to hemodialysis, peritoneal dialysis, ultrafiltration, continuous renal replacement therapy, and Apheresis.
* Provides supervision and direction of Patient Care Technicians and clerical staff; provides direction and education to ICU staff for CRRT.
* Responsible for direct patient care of assigned patients in the Inpatient Renal Replacement and Apheresis Services setting and providing the appropriate treatment technique for assigned patients as prescribed in all modality procedures, as appropriately defined – hemodialysis, peritoneal, continuous renal replacement therapies, ultrafiltration, and Apheresis.
* Assesses patients’ responses to treatment therapy making appropriate adjustments and modifications to the treatment plan as indicated by the appropriately credentialed physician. Communicate problems or concerns to the Inpatient Program Manager, appropriately credentialed physician, patient hospital primary nurse and others as indicated.
* Delivers safe, effective care in a timely an efficient manner.
* Gives organized, concise shift reports for patients on assigned shifts.
Apply high level thinking skills to shift patient schedules to meet needs of more critical patients due to labs, MD order, or patient assessment.
* Responsible for the implementation, administration, monitoring, and documentation of patient’s response to prescribed intradialytic transfusions, including appropriate notification of adverse reactions to physician and appropriate blood supplier.
* Collaborates and communicates with physicians and other members of the healthcare team to interpret, adjust, and coordinate daily patient care plan to ensure continuity of care.
* Initiates and communicates to FMS facility nursing staff and appropriate hospital personnel as needed.
* Accurately documents all treatment information in the individual patient record (ACES) and the hospital record, as needed.
* Cleans and disinfects dialysis machine surface, chair, equipment, and surrounding areas between treatments according to inpatient renal services policies and procedures.
* Conducts all tasks necessary for preparation for dialysis treatment and documents where appropr...
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Type: Permanent Location: Hato Rey, US-PR
Salary / Rate: Not Specified
Posted: 2025-05-23 08:34:21
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Associate Finance Manager - TDC FP&A
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:
Play a crucial role in managing the actual and forecast processes for Total Delivered Cost (TDC) across two business units.
This position requires a combination of technical expertise to enhance the accuracy and efficiency of TDC driver forecasts, along with the ability to effectively communicate monthly changes to key stakeholders.
* Forecasting and Planning: Lead the monthly ABU TDC forecast process.
Gather and analyze inputs from various sources to develop an accurate, key driver-based forecast.
Ensure accuracy across all TDC drivers and communicate results to key stakeholders promptly.
* Variance Analysis: Perform monthly reconciliation of actual results using key metric performance to explain variances to prior forecasts and plans.
Develop strategies to improve forecast accuracy.
* Anaplan Tool Management: Collaborate with the Anaplan COE to understand Anaplan configuration and structure, continuously improving the Anaplan model for higher efficiency, accuracy, and simplification to support FP&A cycles.
* Financial and Operations Control Adherence: Work with the Supply Chain Accounting Team to ensure the application of efficient and effective financial and operating controls.
Support internal control requests as needed.
* Training: Conduct training sessions for Finance business partners to enhance TDC acumen across the organization.
* Cost Savings Transformation: Act as an influential business partner within the Supply Chain organization to identify and drive cost savings opportunities.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
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, incl...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-05-23 08:33:29
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At MTM Transit, it is never just a ride, it's personal.
We understand that our passengers deserve personalized attention and exceptional care and to us, every trip is important.
We have exciting opportunities to join our growing team where your work has a direct impact on the communities we serve.
Our company culture is one of innovation, collaboration, and growth.
If you are passionate, driven, and ready to join a team where your work will directly transform and shape our industry, then we want to talk to you!
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 upon award of contract.
Location: Grand Rapids, MI
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.
* Bach...
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Type: Permanent Location: Grand Rapids, US-MI
Salary / Rate: Not Specified
Posted: 2025-05-23 08:27:34
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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
Internship IP2TIS 2025 - For students in the field of Energy Management or -engineering
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.
Our Global Internship Programme in Innovation & Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.
Are you ready to join a global network spanning 20+ countries, where bright minds collaborate to tackle real-world challenges in Innovation & Sustainability? Do you want to work on impactful projects, shape the future , and drive change from within?
The Opportunity
As a production department at the Penzberg site, we have the potential to make a major contribution to saving energy and significantly improve our sustainability.
Our aim is to reduce energy consumption and achieve our Scope 2 targets through targeted measures.
Be part of this initiative and help us to achieve our environmental goals.
* Responsibility for annual savings in our energy consumption
* Focus on reducing electricity, steam and nitrogen
* Contribute to cost savings by reducing the consumption of energy media
* Positioning our department as a pioneer in sustainable practices
* Support Roche's 10-year ambition to halve the environmental footprint
As an intern on this project, you will work closely with our team to identify energy saving opportunities and develop implementation strategies.
Your tasks will include analyzing current energy consumption, identifying opportunities for savings and developing measures to reduce it.
Main responsibilities:
* You will collaborate on analyzing and reducing energy consumption of electricity, steam and nitrogen.
* You will contribute to the development and implementation of energy saving measures that directly contribute to reducing operating costs and achieving our sustainability goals.
* You will support our team in developing innovative solutions that significantly reduce the environmental footprint of our site.
Learning experiences and growth:
* Gain hands-on experience in a global leading pharmaceutical and diagnostics company.
* Benefit from working in a team with versatile expertise and expand your knowledge i...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-05-23 08:13:09
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ABOUT LCI
The mission of LCI is to provide meaningful employment for the blind and visually impaired.
We accomplish this in four ways:
* EMPLOY: We are one of the largest employers of people who are blind, creating meaningful careers and lasting skills that transform their lives.
* BUILD: We create over 2,000 products and distribute thousands more through manufacturing, retail, nationwide distribution, and e-commerce channels.
* SERVE: Many of our products are sold directly to the federal government.
We were pioneers of “base supply centers,” stores on military bases that employ the blind and visually impaired and provide mission-critical supplies to our nation’s military.
* SUPPORT: We want to end blindness forever.
To that end, we engage in philanthropic efforts for research into blindness and treatment for the visually impaired.
ABOUT THIS ROLE
The MEMS Lab Tech Intern is a support position within an ISO Class 6/7 Cleanroom fabricating nano structures used in the medical device industry.
LOCATION AND SCHEDULE
Durham, NC
Monday-Friday 8:00 AM – 4:30 PM
GMP Lab Environment/ ISO Class 6/7 Cleanroom
KEY RESPONSIBILITIES
* Basic Receiving Inspection duties
* General Cleanroom Maintenance to include maintaining cleanroom logs for temperature, humidity, DI Water Systems, Gas pressures etc.
* Following manufacturing procedures to prepare materials needed in the MEMS fabrication process such as carriers, trays etc.
* Prepare documentation to accompany final release product for sterilization and shipping.
* Work with MEMS Technician as necessary in the prep and calibration of equipment.
* Follow good documentation processes.
QUALIFICATIONS
* Currently pursuing a bachelor’s degree or equivalent in biomedical technology, engineering, or a related field is highly preferred.
* Experience in GMP Lab environment.
Experience in semi-conductor or MEMS cleanroom fabrication and manufacturing lab is a plus.
* GMP Certification preferred
* Ability to follow Manufacturing Procedures, Working Instructions and SOPs under a Quality Management System.
* Manual dexterity to handle small, intricate components and use specialized tools in the lab.
* Ability to work effectively in a team, with strong communication skills to collaborate with the team.
Why LCI?
* Purpose-driven company driven by principles, not profit
* Reach your highest potential: upward mobility, rewarded through hard work
* Competitive salary and compensation
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 information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: Durham, US-NC
Salary / Rate: Not Specified
Posted: 2025-05-23 08:12:47
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Sei pronto/a ad entrare a far parte di un’organizzazione in crescita, globale, specializzata nella produzione e sviluppo farmaceutico, che mette le persone al primo posto? Unisciti ad Adare! Noi lavoriamo a stretto contatto con i nostri partner nell’industria farmaceutica durante tutte le fasi di sviluppo e produzione dei farmaci destinati alla commercializzazione, con l‘intento di migliorare le vite dei/delle pazienti e dei farmaci essenziali per le persone di tutto il mondo.
Ogni ruolo all’interno di Adare ti offrirà un’esperienza unica e personalizzata nonché l’opportunità di avere un grande impatto, fondamentale per il successo della nostra azienda.
Con l’aiuto di persone come te che si dedicano alla nostra missione, Adare migliora vite migliorando la somministrazione dei farmaci !
Unisciti alla nostra missione, unisciti ad Adare!
La nostra proposta:
* Assicurazione sanitaria
* Piano pensionistico
* Benefit previsti da accordo interno
* Crescita professionale e opportunità di avanzamento all’interno dell’azienda
* Premio di partecipazione
* Programma di riconoscimento dei dipendenti.
Siamo alla ricerca di un/una Senior Formulation Scientist che si unisca al nostro Team di Pharmaceutical Development.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Senior Formulation Scientist svolge le attività concernenti lo sviluppo formulativo di prodotti solidi orali dalla scala pilota alla scala industriale, ivi inclusi lotti destinati a studi clinici.
Prepara la documentazione tecnica ed interagisce con i clienti.
Inoltre fornisce formazione, affiancamento e tutoring a scienziati meno esperti, oltre che interagire con i clienti in riunioni dedicate.
La posizione riporta direttamente al Director I, Pharmaceutical Development.
COMPITI E RESPONSABILITA’
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati.
* Svolge il proprio lavoro nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* Elabora ed esegue studi di sviluppo formulativo mirati allo sviluppo di forme solidi orali definite dai clienti o dal Management
* Sviluppa nuovi prodotti impiegando le tecnologie nuove o disponibili dalla pre-formulazione alla produzione su scala industriale
* Esegue in autonomia o supervisiona la produzione di lotti destinati a studi clinici
* Esegue in autonomia attività di technology transfer
* Collabora con le funzioni di Project Management e Business Development nelle attività di progetto quali sviluppo formulativo o technology transfer
* Collabora con Operation, Quality e Regulatory nelle attività di scale up di prodotti dalla fase pilota alla fase industriale
* Esegue in autonomia la stesura di procedure...
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Type: Permanent Location: Pessano Con Bornago, IT-MI
Salary / Rate: Not Specified
Posted: 2025-05-23 08:12:45
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Health Insurance
* Pension Plan
* Benefits
* Career growth and internal opportunities
* Production bonus
* Employee Recognition Programs
We are seeking to hire a Industrialization Senior Specialist to join our Industrialization Team at Italian sites.
If any of the below describes you, we would love to meet you!
Summary
Reporting directly to the Senior Manager, Industrialization - Italy, the Industrialization Senior Specialist supports industrialization department activities by providing her/his technical expertise and collaborating with relevant business units (e.g.
R&D, Manufacturing, Quality, Regulatory, Business Development) during scale-up, process validation, technology transfer, implementation of manufacturing processes and life cycle management of existing products.
This Senior Specialist works in an effective and cooperative manner under deadlines and in respects of Company policies, procedures and regulations.
Responsibilities:
* Carries out his/her work in compliance with company procedures and in accordance with the provisions of the Occupational Health and Safety Management System and Good Manufacturing Practices.
* Assesses technical feasibility, calculates cost of goods, prepares capital investments and capacity analyses of commercial products and Technology transfer opportunities.
* Collaborates with Business Support Team, Industrialization Manager and involved business units providing all the information needed to prepare commercial proposals.
* Works with Pharmaceutical Development (R&D) to scale-up and validate new products from lab to industrial scale and is accountable for industrial scale registration batches.
* Contributes to Life Cycle Management of existing commercial products, including recurrent manufacturing process validation activities, process improvement and optimization.
* Is accountable with Industrialization Team for the Manufacturing Process Validation Plan, writes protocols and reports, and provides technical assistance to Operations and Quality during the manufacturing process validation runs.
* Identifies quality improvement and cost reduction opportunities.
* Provides technical support and project management to add new sources of API, excipients, and packaging components.
...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-05-23 08:12:44
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Sei pronto/a ad entrare a far parte di un’organizzazione in crescita, globale, specializzata nella produzione e sviluppo farmaceutico, che mette le persone al primo posto? Unisciti ad Adare! Noi lavoriamo a stretto contatto con i nostri partner nell’industria farmaceutica durante tutte le fasi di sviluppo e produzione dei farmaci destinati alla commercializzazione, con l‘intento di migliorare le vite dei/delle pazienti e dei farmaci essenziali per le persone di tutto il mondo.
Ogni ruolo all’interno di Adare ti offrirà un’esperienza unica e personalizzata nonché l’opportunità di avere un grande impatto, fondamentale per il successo della nostra azienda.
Con l’aiuto di persone come te che si dedicano alla nostra missione, Adare migliora vite migliorando la somministrazione dei farmaci!
Unisciti alla nostra missione, unisciti ad Adare!
La nostra proposta:
* Assicurazione sanitaria
* Piano pensionistico
* Benefit previsti da accordo interno
* Crescita professionale e opportunità di avanzamento all’interno dell’azienda
* Premio di partecipazione
* Programma di riconoscimento dei dipendenti.
Siamo alla ricerca di un/una Quality Control Junior Analyst (tempo determinato 12 mesi) che si unisca al nostro QC Team di Pessano con Bornago.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Quality Control Junior Analyst svolge le attività analitiche e affini all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP e dalle Procedure Operative Standard, Procedure Analitiche Standard, metodi di analisi, ed altri regolamenti interni, riportando direttamente al/alla Quality Control Laboratory Supervisor.
COMPITI E RESPONSABILITA’
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati.
* Svolge il proprio lavoro nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* Tiene in ordine ed aggiornati i propri quaderni di laboratorio e i propri documenti analitici.
* Esegue operazioni di base di laboratorio, quali: preparazione di reattivi e soluzioni, campionamenti di materie prime, prodotti semilavorati e prodotti finiti, ecc.
* Segue scrupolosamente le disposizioni impartite dai superiori.
* Esegue analisi con tecniche analitiche semplici e complesse, seguendo metodi definiti, in autonomia operativa.
* Adempie alle funzioni per la corretta gestione dei reagenti in accordo alle specifiche procedure.
* Lavora in modo efficace nel rispetto delle scadenze.
* Agisce come rappresentante dell'azienda mostrando rispetto e come ambasciatore /ambasciatrice delle convinzioni e dei comportamenti aziendali.
* Rispetta le politiche, le procedure e le normative in vigore in azienda.
* Svolge ...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-05-23 08:12:43
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Beijing, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in compliance.
Stra...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:33
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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:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Gent, East Flanders, Belgium
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a QA Micro Associate to be in Gent, Belgium!
CAR-T is an innovative blood cancer treatment that uses the strength of the patient's own immune system.
The patient's T-cells are genetically modified to eliminate the cancer cells.
This advanced technology offers hopeful prospects to patients for whom other therapies provide no or insufficient results.
We are therefore working passionately on expanding our capacity for CAR-T treatments in Europe, both at our existing site in Beerse and in Ghent, where we are developing a new production site.
We are looking for strong talents who are eager to participate in this innovative and hopeful venture.
The QA Micro Associate, CAR-T Europe is part of a team responsible for providing microbiological and aseptic oversight and contamination control of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.
The QA Micro Associate will be based in Ghent, Belgium.
You will be responsible for:
* Work with Process Development team, Quality and Operations organization to ensure contamination control of facility to manufacture products, consistent with cGMP and Janssen requirements
* Performs aseptic qualification of manufacturing personnel (e.g.
gowning, aseptic processing).
* Define specific aseptic techniques to be performed for crucial process steps through instructor-led trainings and awareness sessions.
* Drives the Aseptic Oversight program by execution of manufacturing floor surveillance.
* Actively support process microbiological investigations.
* Write relevant QC documents, SOP’s and WI’s.
* Maintain, re-evaluate and communicate key critical inputs to site environmental monitoring program.
* Identify risks and opport...
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Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:26
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
In the R&D Microbiology Centre of Excellence (Beerse, Antwerp, Belgium) there is currently a full-time opening for a microbiology analyst conducting microbial method development, GMP method qualification/validation, and release and stability testing in support of the clinical development portfolio.
R&D Microbiology Analyst
Your Function
* Execute method development and GMP method qualification/validation for a diverse range of microbial assays, such as bioburden testing, bacterial endotoxin testing, sterility testing, etc.;
* Perform release and stability testing on clinical products;
* Coordinate and execute Low Endotoxin Recovery (LER) studies;
* Coordinate and execute Microbial Challenge studies to determine hold time of sterile preparations;
* Author, review and approve development reports, qualification/validation reports and test method descriptions;
* Coordinate laboratory investigations;
* Ensure compliance with regulatory requirements, GMP and safety.
Your Profile
* Bachelor’s degree in Biomedical Laboratory Technology, or equivalent through experience;
* Good knowledge of and experience with aseptic and microbiological techniques;
* Experience with GMP;
* Meet high quality standards when executing experiments;
* Efficient, flexible and dynamic.
Capable of dealing with changes in the planning;
* Team player yet able to organize and execute the work independently;
* Demonstrate sense of urgency;
* Good knowledge of English, both spoken and written.
You will be welcomed in a diverse and coherent team, and will receive proper training by experienced analysts in order to fulfill your role.
Departmental responsibilities
As part of Johnson & Johnson Innovative Medicine, R&D - Discovery, Product Development, and Supply (DPDS) – Analytical Development (AD), the Microbiology CoE has the following responsibilities:
* Providing global support for all microbiology-related aspects during clinical development (R&D) and life cycle management (commercial) of the J&J Innovative Medicine product portfolio (Biotherapeutics and Synthetics).
* Coordinating microbial method development, validation/qualification and transfer activities with internal and external microbi...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:06
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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:
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:
In the Microbiology Centre of Excellence (Beerse, Antwerp, Belgium) there is currently a full-time opening for a pharmaceutical microbiology expert with a proven track record of project management related to microbial method validation, specification setting and control strategy in support of the Biotherapeutics R&D portfolio.
As part of Johnson & Johnson Innovative Medicine, R&D - Discovery, Product Development, and Supply (DPDS), the Microbiology Subject Matter Experts (SME) are responsible for:
* Providing global support for all microbiology-related aspects during clinical development (R&D) and life cycle management (commercial) of the J&J Innovative Medicine product portfolio (Biotherapeutics and Synthetics)
* Coordinating microbial method development, qualification/validation and transfer activities with internal and external microbiology laboratories in compliance with regulatory and internal requirements, GMP and safety regulations
* Microbial specification setting and control strategy
* Author regulatory documents and supporting health authority inquiries in the field of microbiology
* Validation and implementation of innovative microbial technologies for established and new product platforms
* Provide on-demand expertise and solutions for investigations on R&D and commercial products.
Qualifications
Education:
* You hold a PhD degree in Bioscience Engineering, Biology, Biomedical Sciences or similar with a strong expertise in the field of microbiology, or you hold a Master degree in combination with a proven track record in the specific area of pharmaceutical microbiology, in particular in the biopharmaceutical industry.
* The following experience and expertise are considered as important assets:
+ Detailed knowledge of general microbiology as well as familiar with microbiological requirements relevant to the pharmaceutical industry
+ Biological production process knowledge
+ Thorough GMP knowledge
Other:
* Ability to work independently yet also a good team player in an international setting
* Have high moral standards and assure scientific quality
* Good project management skills and able to handle multipl...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:05
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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:
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:
In the Microbiology Centre of Excellence (Beerse, Antwerp, Belgium) there is currently a full-time opening for a pharmaceutical microbiologist with a passion for innovative technologies in support of the Biotherapeutics R&D portfolio.
As part of Johnson & Johnson Innovative Medicine, R&D - Discovery, Product Development, and Supply (DPDS), the Microbiology CoE is responsible for the validation of microbial test methods and the microbial specification setting to assure safety and quality of (bio)pharmaceutical products across the J&J Innovative Medicine portfolio.
Novel therapies require innovative ways of testing, and hereto we are seeking an Innovation Lab lead with a passion for microbiology and new technologies, who manages and coordinates laboratory activities (overseeing 2 analysts) and also participates in the execution, summarizes and reports study results to the local and global project teams, and defines strategic validation and implementation plans in a GMP environment.
Qualifications
Education:
* You hold a PhD degree in Bioscience Engineering, Biology, Biomedical Sciences or similar with a strong expertise in the field of microbiology, or you hold a Master degree in combination with a proven track record in the specific area of pharmaceutical microbiology, in particular in the biopharmaceutical industry.
* The following experience and expertise are considered as important assets:
+ Detailed knowledge of general microbiology as well as familiar with microbiological requirements relevant to the pharmaceutical industry
+ GMP
Other:
* Ability to work independently yet also a good team player in an international setting
* Good project management skills and able to handle multiple projects simultaneously
* People management skills
* Have high moral standards and assure scientific quality
* Strong sense of urgency
* Efficient and flexible attitude
* Excellent communication skills (written and oral)
* You have good knowledge of English (written and oral)
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-23 08:11:04
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
Shanghai, China
Job Description:
* Please kindly note this is an Individual contributor role.
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program...
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:43
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
Limerick, Ireland
Job Description:
An experienced Environmental Specialist who is passionate about their role and has the ambition and drive to develop and continually improve the JJVC Environmental Program while ensuring compliance with the IE Licence, Environmental Regulations, and Corporate standards.
KEY RESPONSIBILITIES
* Lead the sites Environmental Program.
* Ensure compliance with the IE License and other regulatory requirements.
* Ensure compliance with Corporate Environmental Standards, Goals and Objectives.
* Ensure the timely and complaint submission of required reports to the EPA, Corporate and other partners.
* Collect, analyse and report Environmental data as per IE Licence and Corporate requirements.
* Develop and achieve Environmental Goals and Objectives in partnership with Senior Management and other partners.
* Maintain the ISO14001 registration and ensure compliance with all requirements.
* Lead preparations for and execution of Environmental Audits with Regulators, Corporate and Certifying bodies.
* Conduct regular environmental inspections of the facility and systems audits to identify opportunities for improvement.
* Submit all necessary reports to the EPA and Corporate and act as the primary Environmental site contact.
* Collaborate closely with the Sustainability and Energy Teams on site sustainability strategies and initiatives.
* Ensure the effective oversight and management of Key environmental equipment in conjunction with the Facilities department.
* Ensure the effective investigation of any Environmental Events, identification of root cause and putting in place corrective and preventative actions to prevent recurrence.
* Provide Environmental Awareness and training to employees as required.
* Build and maintain strong relationships with stakeholders.
* Support other aspects of the wider EHS Program as required.
EDUCATION AND SKILLS
* Third-level qualification in Environmental Science, Engineering, or a related discipline (B.Sc./B.E.
preferred).
* 5 years of relevant experience managing an Environmental Program at an IE Licensed Facility
* Practical experience of implementing and maintaining an ISO14001 Ma...
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Type: Permanent Location: Limerick, IE-LK
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:39
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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 Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
Job Description:
About Oncology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for MSL to be in Shefayim.
Key Job Activities:
* Keeping abreast of medical and scientific knowledge
* Creating and fostering a network of partnerships with experts
* Working cross-functionally within the company to become a valuable team member
* Providing high level scientific engagement with experts, while utilizing multichannel platforms
* Initiator and coordinator of medical education activities and advisory boards, in alignment with Medical Manager
* Scientific support and training to company sales representatives and other peers
* Supports and initiates evidence generation via research and publications
* Gains valuable scientific insights contributing to the short & long-term strategic plans of the therapeutic area
* Skillful in implementing innovative solutions and ideas for multichannel engagement and data-collection
* Champions medical benefits of products and contributes to the fostering of innovative therapeutic approaches for patient's benefits
* Actively involved in strategy and action plans related to local reimbursement of products
The role is mainly field-based ( 85%) , requires agility with regards to travel & work hours
Requirements:
Education
MD, D.M.D, D.V.M, Ph.D.
(Pharmacy or Science)
Experience:
With preference for:
* Previous experience working in the pharmaceutical industry or research company- an advantage
* High-competency in project & customer-affairs management
Knowledge:
* Deep scientific & clinical kn...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:35
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ERM is hiring an Archaeological Field Technician to support future needs of survey efforts for projects located in Northern California or Southern California.
Archaeological Field Techs will assist with or conduct archaeological field surveys or monitoring.
This is a fixed-term consulting role with a duration of Six months and the possibility of renewal.
RESPONSIBILITIES:
· Digging shovel tests and screening soil;
· Conduct intensive pedestrian surveys consisting of visually inspecting the land surface for presence of artifacts;
· Monitoring alongside construction crews to avoid impacts to resources;
· Bagging recovered artifacts and recording the provenience of the finds;
· Maintaining field notes;
· Compliance with corporate HSE; and
· Performing other duties as assigned or required.
REQUIRED:
· B.A.
in Anthropology
· 2 years of related experience
· Ability to travel extensively throughout Northern or Southern California
· Archaeological field school or prior archaeological field survey experience;
· Ability to work outdoors in variable weather conditions and on varied terrain;
· Ability to work weekends and over 40 hours per week when needed;
· Working knowledge of archaeological survey and monitoring protocols;
· Ability to work in the field for extended periods of time;
· Ability to work independently and as a part of a crew
· Must meet criteria identified in Job Demands & Conditions Analysis for Office and Field Positions.
· Permitted BLM Field Director preferred;
· Master’s in Anthropology preferred
For the Archaeological Field Technician position, we anticipate the annual base pay of $73,207 – $95,761 $35.19/hr – $46.03/hr USD, limited-term, non-exempt.
An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/Flexforce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including Flexforce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
You can apply for this role through https://www.erm.com/careers/apply/ or through the internal careers portal if you are a current employee.
Note: No amount of pay is considered to be wages...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:25
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ERM is hiring a Health & Safety Specialist to support a aerospace client facility in Redmond, WA.
In this critical role, you will be responsible for ensuring safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety is paramount.
This is a full-time (40 hours), limited-term role with a duration of 12 months and the possibility of renewal.
RESPONSIBILITIES:
* Providing health and safety oversight for an aerospace manufacturing facility.
* Oversee general safety and risk programs in an aerospace manufacturing environment – machine safety, LOTO, electrical safety, PPE, fall protection, confined space, etc...
* Communicating with internal stakeholders.
* Developing, reviewing, and/or updating health and safety documentation such as SOPs, JHAs, and safety plans.
* Conduct inspections and audits.
* Participating in the Emergency Response Team.
* Conduct safety training.
* Participate in incident investigation, root cause analysis, and report writing.
* Participating/leading meetings to support ongoing compliance and safety initiatives.
* Writing and submitting status update reports, and other communications.
REQUIREMENTS:
* Bachelor’s in safety or related discipline preferred.
* 3+ years of health and safety experience in a manufacturing environment, aerospace experience preferred.
* Certification such as ASP/CSP highly preferred.
* Experience with High Hazard Work Activity, Confined Space, LOTO, Machine Guarding, and Fall Protection.
* Familiarity with federal/state health and safety regulations.
* Strong MS Office computer skills.
* Excellent written and verbal communication skills.
For the Health & Safety Specialist position, we anticipate the annual base pay of $80,691 – $97,410, $47.56/hr – $55.19/hr, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/FlexForce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including FlexForce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
You can apply ...
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Type: Permanent Location: Seattle, US-WA
Salary / Rate: Not Specified
Posted: 2025-05-23 08:10:18
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Manager of Analytics and Data Science
Location: Niagara Falls, NY (Flexible work options available)
Reports to: Vice President, Research & Developmen, Frank Ortiz
Collain is seeking a skilled and experienced Manager of Analytics and Data Science to join our team.
In this role, you will design and lead the development of innovative software solutions that support healthcare providers in the Long Term and Post Acute Care (LTPAC) sector.
You will collaborate with cross-functional teams to translate business needs into scalable, high-performance software systems and provide technical leadership across projects.
This position will report to Frank Ortiz, Vice President, Research & Development of our Collain business unit.
What your impact will be:
* Lead the design and architecture of scalable software solutions.
* Translate business requirements into technical specifications and system designs.
* Evaluate and recommend tools, frameworks, and technologies.
* Collaborate with cross-functional teams to align architecture with business goals.
* Mentor and support junior engineers and architects.
What we are looking for:
* Bachelor’s or Master’s degree in Computer Science, Engineering, or a related field.
* 10+ years of experience in software architecture and development.
* Proven experience designing complex, scalable systems.
* Strong knowledge of software design patterns and system integration.
* Proficiency in at least one modern programming language.
What would make you stand out:
* Experience in the healthcare technology industry.
* Familiarity with EHR systems or interoperability standards.
* Background in AI or data analytics integration.
What we can offer:
* Opportunity for challenging projects and professional growth
* 3 weeks’ vacation and 5 personal days
* Comprehensive benefit package
* Lifestyle rewards
* Flexible work options
About us:
Collain Healthcare operates in the healthcare technology industry, specializing in solutions for the Long Term and Post Acute Care (LTPAC) sector.
Founded in 2011 and based in Niagara Falls, NY, the company provides electronic health records (EHR) and interoperability solutions designed to help healthcare providers improve operational efficiency and financial performance.
Collain leverages advanced analytics and artificial intelligence to transform healthcare data into actionable insights, supporting better decision-making and aligning with the industry's goals of improved access, outcomes, cost efficiency, satisfaction, and employee well-being.
Our clients primarily include healthcare providers navigating complex care environments.
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-05-22 09:30:32
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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.
This is your opportunity to shape your career through the skills and experience you bring to the role now and by training for the roles you may want in the future.
Our success depends on great teams, where you can thrive and do your best work in a supportive environment.
About the Role
Shape your career by joining Alcoa’s Vacation Student program! Based in WA at our Pinjarra refinery, you’ll have the chance to put your university knowledge into practice, propelling you toward a career path that exceeds your wildest expectations.
Throughout your 12-week paid summer placement, you’ll experience professional growth, technical expansion, and become an integral part of our vibrant community, where inspiration and daily challenges await.
During the program, you will be matched with a senior specialist who will offer hands-on training, mentoring, and coaching.
The program is designed to support you in becoming a creative problem solver, assisting you in completing meaning projects that will be assigned to you.
What’s on offer?
* Exposure to industry and a future career at Alcoa.
* An attractive hourly rate of pay for the hours you work.
* Meaningful project work that provides you with valuable hands-on work experience
* Working locally, in an onsite environment enabling you to return home to friends and family every night.
* Inclusion and diversity networks; shaping a culture where everyone is welcome, respected and heard.
* Be part of our commitment to sustainability, delivering world class technology and innovations that lead the aluminium industry!
* A workplace culture that strongly values your safety.
* Increased opportunity to gain a place in the Alcoa Graduate Program after you have completed your degree
* Access to the Alcoa Live Well program with a selection of health & wellbeing discount offers to help you live your best life!
What you’ll be doing
As an Occupational Hygienist Vacation Student at Alcoa, you will learn, grow and develop hands-on experience and expertise in:
* Based on site at our Pinjarra Alumina Refinery.
* Assigned a project that both delivers real value to the business and provides you with hands-on industry experience.
* Involved in conducting ongoing surveillance programs including workplace exposure monitoring.
* Exposed to hazardous materials risk assessment and management.
* Assisting in the identification and verification of exposure controls for chemical, physical and biological hazards.
You will be given an appropriate level of responsibility to handle assigned project(s), utilizing your innovative thinking, eagerness to learn, and passion for growth to make meaningful contributions to the business.
In our open-minded...
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Type: Permanent Location: Pinjarra, AU-WA
Salary / Rate: Not Specified
Posted: 2025-05-22 09:30:17
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Alternant(e) Assistant Manager Operations
Job Description
A propos du poste
En tant que personne, vous êtes un apprenant – quelqu’un qui prend toujours l’initiative d’améliorer les choses et d’entraîner les autres avec vous.
Vous vivez votre vie en accord avec les valeurs les plus élevées d’intégrité et de qualité, en veillant toujours à ce que vos responsabilités deviennent une réussite à long terme.
Dans le cadre de ce rôle d’apprenti opérateur de production, vous nous aiderez à fournir de meilleurs soins à des milliards de personnes dans le monde.
Cela commence par VOUS.
Nous recherchons un(e) alternant(e) Assistant Manager Operations en contrat d’apprentissage de deux ans au sein de notre usine Kimberly-Clark de Villey Saint-Etienne (54).
Vous serez au cours de votre contrat d’apprentissage amené(e) à travailler sur les missions suivantes :
* Déploiement des Indicateurs de Performance :
Déployer des indicateurs de performance pour la sécurité, l'environnement, la qualité, l'adhérence au planning de production, la performance des machines et les ressources humaines.
Déployer des paretos sur les indicateurs de panne, déchets et perte de vitesse concernant la performance des machines.
Sensibiliser les équipes de production à l'importance de la performance et assurer le déploiement des indicateurs dans toutes les équipes.
* Accompagnement au Déploiement de l’outil SAP PM :
Aider l'équipe projet SAP PM à déployer notre nouvel outil de GMAO (Gestion de Maintenance Assistée par Ordinateur).
Constituer les nomenclatures de pièces.
Accompagner les équipes dans l'utilisation du nouvel outil SAP PM.
A propos de nous
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
Vous connaissez déjà nos marques légendaires, tout comme le reste du monde.
En fait, des millions de personnes utilisent les produits Kimberly-Clark tous les jours.
Nous savons que ces incroyables produits Kimberly-Clark n’existeraient pas sans des professionnels talentueux, comme vous.
Chez Kimberly-Clark, vous ferez partie de la meilleure équipe qui s’engage à stimuler l’innovation, la croissance et l’impact.
Nous sommes fondés sur plus de 150 ans de leadership sur le marché et nous sommes toujours à la recherche de nouvelles et meilleures façons de performer - c’est donc là que vous avez une porte ouverte sur les opportunités.
Tout est là pour vous chez Kimberly-Clark.
Guidé par un objectif.
Piloté par vous.
A propos de vous
Vous performez au plus haut niveau possible et vous appréciez une culture de la performance alimentée par une bienveillance authentique. Vous voulez faire partie d’une entreprise qui se consacre activement à la durabilité, à l’inclusion, au bien-être et au développement de carrière.
Vous aimez ce que vous faites, surtout lorsque le travail que vous faites fait une diff...
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Type: Permanent Location: Toul Cedex, FR-54
Salary / Rate: Not Specified
Posted: 2025-05-22 09:27:47
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SRI Healthcare, LLC, a Subsidiary of NOVO Health Services offers a healthcare service that provides a total and unique opportunity for hospitals to source their Sustainable Reusable Sterile Packs as well as other sustainable healthcare linens such as DermaTherapy®, Isolation Gowns, Sterilization Wrap, and cubicle/privacy curtains.
SRI's products and services help Healthcare providers attain their sustainability goals, improve surgeon and staff satisfaction while ensuring continuity of supply.
SRI operates three regional processing facilities located in Raleigh, NC, Chattanooga, TN, and Mason, OH.
Our state-of-the-art, FDA-regulated service centers provide daily processing, assembly, and delivery of reusable products required for surgery.
SRI is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with Sterilized Reusable Surgical Solutions.
Get to know us: SRI Health Care, with headquarters in Atlanta, GA, offers linen management solutions to the healthcare industry.
SRI keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs.
SRI’s wide range of service programs offer a variety of options to provide a seamless, single source distribution system.
SRI’s regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes.
SRI Health Care is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with both Healthcare Laundry Services as well as Sterilized Reusable Surgical Solutions.
Job Summary:
We are currently looking for a Team Lead Soil Sort, at our Chattanooga, TN Healthcare Laundry facility.
We are looking for someone who is confident in decision making, can act quickly, and has excellent communication skills.
If you are ready to make a commitment to measurable performance and continuous improvements, then we want to hear from you!
The successful candidate:
* Know all soil sort operations, including Standard Operating Procedures and Q.A.
functions, and ensure adherence by soil sort personnel to established standards.
* Train all new soil sort employees.
* Make recommendations to facility management on soil sort methods or production standard changes.
* Assist facility management in employee hiring process and evaluations as needed.
* Keep accurate records to comply with written Standard Operating Procedures.
* Facility management in scheduling of any testing, validation, etc.
* Maintain cleanliness
* Ability to read and understand all Standard Operating Procedures.
* Other duties as assigned.
Job Requirements:
* Extremely organized and detail-oriented.
* Able to keep precise records.
* Good interpersonal skills.
* Able to train new...
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Type: Permanent Location: Chattanooga, US-TN
Salary / Rate: Not Specified
Posted: 2025-05-22 09:24:03
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Breda, Netherlands
Job Description:
We are looking for a driven Manager Clinical Operations to join our growing Clinical Operations team in Belgium (Beerse) and The Netherlands (Breda).
As a Clinical Research Manager, you will manage a team of Local Trial Managers (Local project managers), Site Managers (Clinical Research Associates) and Clinical Trial Assistants, with a strong focus on staff performance, people development, training/onboarding and resource management.
You are responsible for the successful implementation and execution of phase Ib-IIIb trials from country feasibility through study close-out while keeping clear oversight of timelines, budget, quality & performance indicators and compliance with Standard Operating Procedures (SOPs), Health Care Compliance (HCC) and local regulatory requirements.
We are seeking to hire a strong leader, who is a team player, with quick learning and problem-solving abilities.
You will contribute to the creation of the country strategy in order to optimize ways of working, drive innovation, and strive for continuous improvement and future readiness.
You will be part of a hardworking, enthusiastic, and committed team eager to deliver and helping to improve the lives of millions of patients.
Principal Responsibilities:
* People management: Provide line management to your team including goal setting, performance evaluation and talent development; Build, hire and train a fully effective team; Conduct accompanied site visits; Evaluate and forecast resource needs and manage your team's workload.
* Trial delivery & oversight: Accountable for robust feasibility processes and oversight of site selection.
Responsible for implementation, execution and monitoring of trials in assigned therapeutic area(s).
Empower your team to deliver on your team's quality and performance objectives.
Ensure inspection readiness at all times, adherence to ICH-GCP, local legislation and relevant SOP's.
Support your team in issue resolution and stakeholder management.
Support audits, inspections and timely CAPA resolution.
Build and shape internal and external network in assigned therapeutic area.
* Continuous improvement & organizational change: Lead implementation of innovation and change in the local organization; Cul...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-22 08:49:27
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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:
Enterprise Management
Job Sub Function:
R&D Management
Job Category:
People Leader
All Job Posting Locations:
Galway, Ireland
Job Description:
Johnson & Johnson MedTech Neurovascular are looking for an R&D LCM (Lifecycle Management) Manager / Principal Engineer
Location: Ballybrit, Galway
Johnson & Johnson MedTech Neurovascular
J&J MedTech Neurovascular is a global leader in neurovascular care.
Our commitment to changing the trajectory of stroke is inspired by our long heritage and dedication to helping physicians protect people from a lifetime of hardship.
J&J MedTech Neurovascular offers a broad portfolio of devices used in the endovascular treatment of hemorrhagic and ischemic stroke.
What is it like to work at J&J MedTech Neurovascular Galway?
* Culturally, we are putting the needs of Our Credo stakeholders first through pursuing the highest standards of quality, compliance, and ethics, ensuring everyday actions contribute to Our Purpose.
* We are continuing to better our understanding of clot science, through our Neuro Thromboembolic Initiative (NTI).
This is a commitment to advance the treatment of stroke through interdisciplinary collaboration and investment in clot and stroke research.
How we understand clots and their behaviour enhances our opportunity to design devices that improve patient outcomes and, overall, advance the treatment of acute ischemic stroke.
* Strong new product pipeline and the fastest growing medical device company within J&J in 2021.
* From a People perspective, we invest in our people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation.
This is empowered through our employee resource groups (ERGs) focused on further balances of gender, nationality, capability and more, including the additional attracting of qualified diverse candidates for our open roles.
Job Summary:
Johnson & Johnson MedTech Neurovascular is recruiting for a R&D LCM Manager in Galway Ireland.
The R&D LCM Manager will be responsible for managing design changes and sustaining activities providing technical leadership and judgment to a team of engineers in the life cycle of a portfolio of devices to treat ischaemic and haemorrhage stroke.
The R&D LCM Manager is also responsible for co-ordinating the activities of a multi-disciplinary team to ensure the successful compl...
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Type: Permanent Location: Galway, IE-G
Salary / Rate: Not Specified
Posted: 2025-05-22 08:48:52
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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:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
The Analyst, Global Finance Master Data, is responsible for service delivery of specific Global Finance Master Data process functions serviced by GS Finance-Manila in J&J.
Key Responsibilities:
* Perform day to day operations of Financial Master Data team which includes maintenance of GL Accounts, Profit Center, Cost Center, Internal Order and Exchange Rate in line with Global DTP and defined standards
* Proactively identify, rectify and follow-up errors and causes of errors.
* Ensure timeliness, accuracy and quality of work and service by Finance Master Data team through regular review, checks and approval.
* Resolve complex or critical process issues which go beyond Finance Master Data team member’s capabilities.
* Handle risks through mitigation.
* Ensure that documentations are complete and up-to-date.
* Initiate, monitor and review systems’ accesses of the team.
Identified gaps are to be
* Support auditors and legal authorities with the execution of required activities – ensure staff are available as the need arises.
* Ensure strong internal controls are in place, in order to achieve “adequate” internal and external audit ratings.
* Accurate and timely month-end reporting.
Meet all corporate and regional deadlines
Qualifications:
* Bachelor's Degree in Accountancy or Finance
* Open to fresh graduates
* Experience in Finance Master Data Management or Account to Report is preferred
....Read more...
Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-05-22 08:48:06
