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CE QUE TU FERAS AU QUOTIDIEN
Tes missions :
- Tu conduiras tout type d’engin de manutention.
- Tu t’assureras que la marchandise est réceptionnée, stockée, préparée et expédiée de manière la plus efficace et optimale dans le respect des règles de sécurité et de qualité.
- Tu prépareras les commandes en prélevant les colis et en appliquant les règles de sécurité et de qualité liées à son activité.
- Tu devras effectuer les contrôles quantitatifs et qualitatifs des marchandises entrantes et sortantes.
- Tu contribueras au maintien d’un environnement de travail propre et sûr.
- Tu effectueras des mouvements de palettes suivant les objectifs définis dans le respect des règles en vigueur dans l’entreprise.
- Tu effectueras de la manutention manuelle liée à l’activité logistique.
- Tu devras informer le chef d’équipe de tout risque lié à la sécurité des hommes et des biens.
- Tu devras signaler toutes anomalies constatées dans le cadre de l’exécution de ces tâches.
Rémunération : A partir de 1 855 € brut par mois.
Tes avantages, en plus de ton salaire :
• Une prime de 13ème mois versée en 2 fois.
• Une remise de 15% sur tes achats IKEA.
• Une part de rémunération variable liée à la performance économique globale.
• Une prime de transport de 1,50€ à 3,90€ par jour travaillé en fonction de ton lieu d’habitation.
• Une solution de restauration complète à petit prix.
• Des boissons chaudes offertes à volonté.
• Une mutuelle d'entreprise avantageuse dès ton arrivée.
• Un plan d'épargne entreprise.
• Une valorisation de ton ancienneté (prime et jours de congés supplémentaires).
QUI TU ES
Pour ce poste, aucun diplôme ou niveau d'étude n'est requis, nos formateurs sont là pour t'apprendre le métier !
- Tu es positif et orienté solution.
- Tu es dynamique, minutieux et attentif au respect des règles de sécurité.
- Tu aimes le travail d'équipe mais tu sais aussi travailler de façon autonome.
- Tu maîtrises la langue française et les bases de mathématiques (nécessaire pour utiliser nos outils digitaux et mener à bien tes missions).
- Tu as une formation en entreposage/magasinage et/ou une première expérience en logistique ?
- Si tu as ton CACES cela facilitera ta période d'intégration, sinon nous délivrons aussi une autorisation de conduite interne IKEA à nos collaborateurs et collaboratrices.
- Ta visite médicale renforcée est à jour.
Situé à 20km de Lyon, le dépôt IKEA de St Quentin Fallavier recense environ 440 collaborateurs et collaboratrices travaillant sur une surface de plus de 100 000 m2.
Notre activité est dédiée exclusivement à la livraison directe aux clients.
Comme le dit Nicolas, Employé logistique sur notre plateforme : "pas de clients mais beaucoup de mouvements", alors même si le client n'est pas au milieu des allées, c'est lui que nous devons satisfaire dans les meilleurs délais !
La diversité est au cœur de nos préoccupations c'est pourquoi nous accueillons près de 33 nationalités différentes.
Ton rythme de travail :
Les jours de travail s’organisent en 2x8h : Tu seras une semaine de l’équipe du matin (de 6h à 13h20) et la semaine suivante de l’équipe de l’après-midi (de 13h30 à 20h50) en alternance.
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Type: Permanent Location: St. Quentin Fallavier, FR-ARA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:17:28
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På DHL arbetar vi med att få våra kunders vardag att fungera.
Som ett av de ledande företagen i världen inom logistik, ser vi till att våra kunder får leverans av varor och material.
Utan transporter stannar samhället, vi har ett viktigt uppdrag - Förena människor, förbättra liv. Som medarbetare hos oss är du en viktig nyckelspelare.
DHL Freight Sweden i Ljusdal är lokaliserat till DHL Express AB kundservice lokaler.
Här supporterar vi våra kunder som har en av DHL Freights e-lösning, samt support åt alla våra ca 2000st Servicepoint ombud runt om i Sverige.
Vi är en liten grupp så hos oss är det viktigt att man vill jobba som ett team för att trivas.
Teamet består av 8st advisors.
Arbetsuppgifter och ansvar
Du kommer jobba i ett team med många olika arbetsuppgifter och utmaningar där service är nyckeln.
Vi supporterar våra kunder och ombud måndag- fredag mellan 08:00-17:00 där frågor kan vara av både teknisk och service karaktär och då bred kompetens krävs utbildas man kontinuerligt.
Support både via samtal och e-post.
Profil & Bakgrund
För att lyckas i det här jobbet behöver du ha en stor servicekänsla och vilja att anta utmaningar och utvecklas i takt med företaget och våra tjänster.
Som Customer Service e-Com/Partner support advisor jobbar man inom ett brett område.
Nedan kännetecknar dig som person:
* Lugn, trygg och ha vilja att jobba i ett lag med stor teamkänsla.
* God datavana och tekniskt intresserad.
* Kunna kommunicera i Svenska och Engelska i tal och skrift.
Erfarenhet av teknisk support är meriterande, men inget krav.
Tjänsten är ett sommarvikariat med 100 % tjänstgöringsgrad.
Tjänsten är placerad i Ljusdal.
Vad erbjuder vi dig?
Vi på DHL trivs och många av oss har jobbat här länge.
Vi är ett företag som ser våra medarbetares utveckling och potential – vi vågar satsa på våra medarbetare! I det stora globala, och internationella bolaget som vi är, har vi en härlig teamkänsla med familjär stämning där vi respekterar varandra.
Här finns mycket medarbetarengagemang samt humor och vi tycker om att fira våra framgångar.
Vi är certifierade i Top Employer vilket innebär att vi är en arbetsgivare som erbjuder den bästa arbetsmiljön för medarbetare att utvecklas både professionellt och personligt.
Miljö och hållbarhet är viktigt för oss, vi arbetar ständigt med att utvecklas för att ligga i framkant, vilket uppmärksammas och ger resultat.
Vi tar ansvar och blev bland annat utsedda till branschvinnare av Sustainable Brand Index B2B för tredje året i rad.
Vill du också vara med? Välkommen med din ansökan 15:e april, urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdatum.
Vid frågor, vänligen kontakta Anders Kämpe på email: anders.kampe@dhl.com eller 0651-342401.
Häng med oss bakom kulisserna, följ oss på Instagram
Eller kika närmare på DHL - vårt varumär...
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Type: Contract Location: Ljusdal, SE-X
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:55
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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:
Legal & Compliance
Job Sub Function:
Enterprise Compliance
Job Category:
Professional
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Regulatory Compliance Manager, to be located in Schaffhausen, Switzerland.
Today, IM Schaffhausen is one of the largest pharmaceutical manufacturers in Switzerland supplying all the major global markets.
The Schaffhausen facility is a Johnson & Johnson strategic launch and growth site.
If you’re passionate about compliance and eager to make a difference in a collaborative environment, we want to hear from you! Join us and help us uphold our commitment to excellence!
Your key responsibilities
* Maintain the site’s inspection readiness by providing guidance in routine readiness activities, self-assessments, improvement initiatives, and projects related to Quality Systems.
* Assist in Front Office/Back Office activities during external audits, offering guidance and support in response to observations.
* Assess compliance in failure investigations, root cause identification, action plan development, and effectiveness monitoring.
* Drive compliance initiatives by implementing proactive projects.
* Champion Johnson & Johnson Standards and applicable pharmaceutical regulations, ensuring the site’s adherence while fostering collaboration across teams.
* Develop, coordinate, and execute the site’s internal audit program.
* Represent Regulatory Compliance in various forums and promote a culture of continuous improvement through performance metrics and best practices.
* Collaborate on independent audits and special assessments while refining compliance strategies.
Qualifications
Education:
* A minimum of a bachelor’s degree or equivalent experience in Science or related field.
Experience and Skills
Required:
* Minimum of 7 years in a GMP-regulated environment, with at least 2 year focused on quality, manufacturing or regulatory compliance.
* In-depth understanding of compliance requirements related to medicinal products
* Proven experience in performing GMP audits.
* Proven experience in preparing and supporting inspections.
* Strong analytical and interpersonal skills with a solution-oriented mindset.
Preferred:
* In-depth knowledge of aseptic technique and large molecule manufacturing
* Experien...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:46
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Manatí, Puerto Rico, United States of America, San Lorenzo, Puerto Rico, United States of America
Job Description:
Responsibilities:
* Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Dedicated to developing, manufacture, and market quality products.
* Reviews and analyses quality trends with the manufacturing team.
Considering the quality trends provides direction in terms of setting work priorities for process enhancement.
* Provides guidance to manufacturing supervisors to ensure that effective in-depth investigations are performed.
* Provides leadership and guidance to cross functional, multilevel technical teams to assure causes of non-conformance are identified and understood and that sound corrective/preventive actions are implemented.
Evaluation of the implemented corrective and preventive actions against trends to assess effectiveness of the same.
* Leads investigations of the negative trends and in alignment with the Process Engineer and the Manufacturing Manager, facilities the implementation process.
* 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 QSR/ISO requirements).
* May lead a number of CAPA and should recommend CAPA’s based on negative trends.
* Handles, prepares data and present product escalation investigations (PRE’s), near misses and QRB.
* Leads in-process investigations with a multifunction team to determine root causes and provides recommendations for corrections on preventive actions.
* Handles preliminary investigations of product complaints, analysis, trends and recommendations or leads corrective/preventive actions.
* Provides technical supervision to multilevel, cross functional teams.
Provides supervision to technical professionals such as Process Quality Technicians, College Recruits, C...
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Type: Permanent Location: San Lorenzo, US-PR
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:38
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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:
Legal & Compliance
Job Sub Function:
Enterprise Compliance
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Senior Analyst, Trade Compliance in Raritan, NJ.
The Senior Analyst Trade Compliance is responsible for facilitating data extraction, collection, cleansing and preparation to support the Segment’s trade compliance and operation’s needs.
This position works closely with Trade Controls and Trade Operations to address data needs to enable maturity of the Segment Trade Compliance program, with an initial focus on export controls and trade sanctions.
Key Responsibilities:
* Collaborate with Regional Trade Operations, Global Trade Controls, Health Care & Compliance and Global Legal Organization on identification structured and unstructured trade data needs.
* Implement continuous improvement lean initiatives
* Serve as the segment data super user responsible for the collection and distribution of data to fulfill government filings, reporting, audits and 3rd party provider requests.
* Support the Segment SAP GTS efforts, with initial focus to trade compliance master data needs to ensure effective alignment with the Global Trade enterprise technology strategy including data requirements.
* Assist with the creation of Segment cross-border trade flow, data and system mapping to support critical initiatives.
* Work in partnership with the Segment Customer Master and Product Master Governance teams to ensure ERP data completeness and accuracy to facilitate compliant exports and imports.
* Support non-ERP systems and tools data activities to meet trade compliance data standards.
* Monitor request tracker daily to ensure proper data collection performance
Qualifications
Education:
* A minimum of bachelor’s degree and/or University degree is required; focused degree in Business Administration, Supply Chain Management or related field preferred
Experience and Skills:
Required:
* Minimum four (4) years of relevant professional work experience
* International Trade (Import/ Export and Drawback processes)
* Trade compliance experience.
* Understanding of data standards, data architecture and related governance.
* Proven attention to details.
* Proficiency in English including verbal and written communicati...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:34
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Professional
All Job Posting Locations:
Neuss, North Rhine-Westphalia, Germany
Job Description:
Wir sind J&J Innovative Medicine
Wir gehören zur Unternehmensfamilie von Johnson & Johnson, einem der größten Gesundheitsunternehmen der Welt.
Wir kämpfen gegen schwerste Krankheiten bis sie nur noch dort zu finden sind, wo sie hingehören: In Geschichtsbüchern.
Bei J&J Innovative Medicine Deutschland arbeiten wir alle gemeinsam für dieses große Ziel.
Wir finden neue Wege, um Medikamente zu entwickeln und sie allen Menschen zur Verfügung zu stellen, die sie brauchen.
Eine spannende Aufgabe, die wir mit Leidenschaft verfolgen.
Das Schöne ist, dass wir dabei auch noch Spaß haben: Wir sind ein Team.
Bei uns gelten offener Dialog und gegenseitige Wertschätzung mehr als Hierarchien.
Wir kämpfen gemeinsam und wir lachen gemeinsam.
Wir haben schon vieles für Patienten erreicht, das vorher unvorstellbar war.
Und wir wollen noch viel mehr erreichen.
Dafür brauchen wir Sie in unserem Team am Standort Neuss, zwischen den Rhein-Metropolen Köln und Düsseldorf.
Mit unserer klinischen Forschung (Bereich GCO – Global Clinical Operations) schaffen wir die Voraussetzungen, damit später neue Medikamente für z.T.
schwerwiegende Erkrankungen zugelassen werden können.
Wir sind für die Durchführung der klinischen Prüfungen, die die Datengrundlage für Zulassungsdossiers bilden, zuständig.
Dabei arbeiten wir mit vielen Partnern im Gesundheitswesen zusammen.
Für unser Team in Deutschland suchen wir eine(n)
Clinical Research Associate (m/w/d) (Associate Site Manager / klinischer Monitor)
Ihre Aufgaben und Verantwortlichkeiten:
Als Clinical Research Associate (CRA) sind Sie der wichtige Partner vor Ort zwischen uns als Sponsor und dem Prüfzentrum.
Sie begleiten die Durchführung der klinischen Prüfungen an den Studienzentren vor Ort, um auf mögliche Inspektionen durch die Behörden vorbereitet zu sein und zwar durch Einhaltung des Prüfplans, der SOPs des Unternehmens, der GCP- und anderen geltenden Vorschriften und Richtlinien vom Beginn der Studie bis zum Abschluss.
Zu den Aufgaben gehört die Unterstützung bei der Bewertung der Eignung und die Auswahl der Prüfzentren die Initiierung von Prüfzentren sowie das Monitoring der klinischen Ergebnisse und schließlich die Abschlussarbeiten am Ende einer klinischen Prü...
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Type: Permanent Location: Neuss, DE-NW
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:28
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Channel Sales – MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Ciudad de Mexico, Mexico
Job Description:
Responsabilidades:
• Gerenciar las operaciones comerciales de Vision Care en el territorio Mexicano, responsable del desarrollo de ventas y manejo rentable de las cuentas a su cargo, para asegurar el objetivo comercial de la compañía
• Diseñar el Joint Business Plan en conjunto con el cliente para ejecutar la estrategia de cada Unidad de Negocio, y potencializar el portafolio acorde a sus necesidades y del tipo de consumidor de su negocio
• Gestionar la cartera de clientes asegurando la cobranza y el correcto seguimiento de pagos a clientes de las diferentes actividades del plan promocional, y del curso normal del negocio
• Catalogar las innovaciones de productos con una correcta colocación de inventario de acuerdo con los planes de la Unidad de Negocio
• Asegurar la disponibilidad y correcta dispersión de los productos a través del seguimiento de demanda, niveles de inventario, facturación y cobranza
• Identificar y mantener los básicos en los clientes, distribución, categorización de los productos por punto de venta, estrategia de precios etc
• Implementar la estrategia de negocio de cada marca en el cliente
• Identificar oportunidades de crecimiento para los clientes basados un conocimiento profundo y exhaustivo de los mismos
• Participar activamente de procesos claves de la compañía relacionadas con el proceso de demanda, desarrollo de inversiones de trade marketing, manejo de cartera, mejora del flujo de caja entre otros
• Trabajar en conjunto con Asuntos Profesionales y Marketing para planificar y ejecutar Congresos profesionales u otros eventos educativos para los ECP
• Monitorear y reportar las actividades competitivas
• Cumplir con las políticas y el cumplimiento normativo de la empresa, incluyendo (pero sin limitarse a) Calidad, Health Care Compliance, Safe Fleet y Política de Conducta de Negocios
• Viajes según sea necesario para acompañar los clientes, para atender reuniones de negocio y entrenamientos
Requisitos:
• Licenciado en Ingeniería, Administración de Empresas, Economía o Ciencias de la Salud
• Maestria deseable
• Inglés fluido deseable
• 5 años de experiencia en ventas en el campo comprobable
• Deseable conocimiento y experiencia en el ...
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Type: Permanent Location: Ciudad de Mexico, MX-CMX
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:23
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Communications & Corporate/External Affairs
Job Sub Function:
External Communications
Job Category:
Professional
All Job Posting Locations:
São Paulo, Brazil
Job Description:
We are searching for the best talent for Corporate Communication & Public Affairs Manager to be in São Paulo, Brazil.
Purpose:
The Corporate Communication & Public Affairs Manager will develop and implement a data-driven strategy to enhance J&J Innovative Medicine Reputation in Brazil, leading the institutional external communication agenda, encompassing digital initiatives, media relations, and crisis management.
The professional will be also responsible for developing strategies to shape the external landscape to ensure a public policy environment that is conducive to the success of our portfolio, and thereby, to patient access.
The main focus is on strengthening the value of innovation and access narrative and the channels that we use to reach critical stakeholders including advocacy groups, key opinion leaders, policymakers and decision makers, working in close collaboration with External Affairs and Patient Advocacy colleagues who manage external stakeholder relationships.
Acts independently to guide senior management on the external communication engagement strategy and on the approach to a variety of key public announcements and subsequent press releases, including specific announcements for external audiences related to public, community, government, and investor relations.
Ensures corporate reputation, confidentiality, and brand standards are consistently upheld.
Works in partnership with other areas to analyze key policy topics where the organization needs to shape externally, building and executing engagement plans and with the cross-sector team to reinforce J&J Brazil reputation.
You will be responsible for:
• Acts as a developing subject matter expert and monitors business critical issues in public affairs and tracks legislative and regulatory changes.
• Applies developing expertise on public affairs to review policies that may impact organizational objectives.
• Creates informational and marketing materials and develops optimal delivery methods; includes writing, editing, and managing necessary review and approval processes.
• Consults on briefing and other materials for management ahead of meetings or events with public officials and members of the press.
• Executes communicati...
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Type: Permanent Location: São Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:18
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CE QUE TU FERAS AU QUOTIDIEN
Avec l'appui du responsable de service Vente, ton rôle est de maximiser les ventes en t'assurant que ta zone de responsabilité soit toujours en parfait état.
Dans un magasin IKEA le département Vente est constitué du secteur Exposition (vente d'articles meublant), Marché (boutiques d'accessoires) et Libre service-meubles.
Tu veux voir à quoi ressemble notre ambiance de travail ? Clique sur Postule et découvre au bas de l'annonce complète le métier en vidéo.
Cela ne t'engage à rien ;)
• Tu abordes avec respect les visiteurs pour en savoir plus sur leurs besoins et les guider dans leur choix grâce à ta connaissance approfondie de nos produits et services.
• Tu veilles à ce que ta zone soit impeccable et facilite le parcours client : modèles d’exposition en parfait état, mise en avant des nouveautés et produits les plus demandés, propreté du rayon, étiquetage correct.
• Tu t'appropries les objectifs de ton département et tu sais comment y contribuer, notamment en pilotant les ventes et en assurant une disponibilité optimale des produits de ton rayon.
• Tu n'hésites pas à donner un coup de main à tes collègues au besoin.
Rémunération : à partir de 1840 € brut mensuel (salaire de référence pour un temps plein).
Outre ton salaire de base qui rémunère ton travail, tes compétences et tes responsabilités, tu bénéficieras notamment de :
• Une prime de 13e mois.
• Une part de rémunération variable liée à la performance économique globale.
• Une mutuelle santé offrant des prestations de qualité, dès ton arrivée.
• Une prime d'ancienneté (au-delà de 2 ans).
• Des congés supplémentaires pour ancienneté (au-delà de 3 ans).
• La possibilité de prendre un déjeuner pour moins de 3€.
• Une remise personnelle de 15% sur tes achats chez IKEA.
QUI TU ES
IKEA, leader international de solutions d’aménagement de la maison, poursuit depuis plus de 40 ans son développement en France avec toujours la même vision : « améliorer le quotidien du plus grand nombre ».
Animés par notre culture et nos valeurs, nous sommes passionnés par la vie à la maison.
Chez IKEA, nous vivons la culture suédoise au quotidien.
Et, comme le font les Suédois, nous nous tutoyons tous, peu importe notre poste ou notre unité.
C'est pourquoi nous le faisons aussi dès cette annonce et pendant tout le processus de recrutement !
* Tu es dynamique et à l’aise dans le contact avec les clients.
* Tu aimes le travail d'équipe
* Tu es organisé(e) et tu fais preuve d’initiative pour gérer les priorités et t’adapter selon les situations.
* Tu es motivé(e) par le désir de développer tes compétences et de servir au mieux les clients.
* Tu as déjà travaillé dans la vente ou le service client et le secteur de l’aménagement et de la décoration t’attire particulièrement.
Pour en savoir plus sur notre processus de recrutement c'est par ici
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Type: Permanent Location: Henin Beaumont, FR-HDF
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:15
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Financial Planning & Analysis
Job Category:
Professional
All Job Posting Locations:
Ringaskiddy, Cork, Ireland
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/.
We are an equal opportunity employer and value diversity at our company.
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status or disability status.
Johnson & Johnson MedTech, located in Ringaskiddy Cork, is the largest, most innovative and comprehensive Orthopedic and Neurological business in the world. J&J companies will offer an unparalleled breadth and depth of products, services and programs in the areas of Joint Reconstruction, Trauma, Spine, Sports Medicines, Neurological, Power Tools and Bio Materials.
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years.
We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people.
The primary location for this role is Cork, Ireland.
JOB TITLE: Make Senior Finance Analyst
DEPARTMENT: MAKE FINANCE
JOB PURPOSE:
The Make Senior Finance Analyst will be part of the Make Finance Team whose responsibility is to provide business support and accounting analysis across multiple areas within the Make Finance Team. The Make Finance Team provides support to the Cork Manufacturing Plant, which is the largest manufacturing plant in the J&J MedTech Joints Network. This position will be required to support many aspects of the business in the manufacturing plant for J&J MedTech which is based in Ringaskiddy, Co.
Cork.
___________________________________________________________________________
ORGANISATIONAL INTERFACES:
The role may require interfacing with various functions across Johnson and Johnson, and a broad range of internal and external stakeholde...
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Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:13
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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:
Career Programs
Job Sub Function:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
Bogotá Distrito Capital, Colombia
Job Description:
Acerca de Johnson & Johnson MedTech Cardiovascular
Con el impulso por la innovación en la intersección de la biología y la tecnología, estamos desarrollando la próxima generación de tratamientos más inteligentes, menos invasivos y personalizados.
¿Te apasiona mejorar y ampliar las posibilidades de Cardiovascular? ¿Preparad(o/a) para unirte a un equipo que está reimaginando cómo nos curamos? Nuestro equipo de Cardiovascular desarrolla soluciones líderes para la electrofisiología y el accidente cerebrovascular.
Te unirás a una orgullosa herencia de elevar continuamente los estándares de atención para pacientes con ictus y fibrilación auricular (AFib).
Tus talentos únicos ayudarán a pacientes en su viaje hacia el bienestar.
Obtén más información en https://www.jnj.com/medtech.
Estamos buscando al mejor talento para la posición Aprendiz SENA que estará localizada en Bogotá, Colombia.
Propósito: Nuestro programa tiene como objetivo atraer y contratar talentos como TÚ, que actualmente estén cursando carreras técnicas y tecnológicas, que busquen aprender durante su etapa productiva y tengan la mejor actitud para asumir grandes desafios.
El aprendiz del SENA que se incorpore al área de marketing desempeñará funciones esenciales para el buen manejo administrativo del área.
A continuación, se detallan los requerimientos necesarios para cumplir con estas funciones de manera efectiva.
Principales Responsabilidades:
* Creación, adaptación y aprobación de materiales promocionales.
* Creación de órdenes de compra para las diferentes actividades de la unidad de negocio.
* Creación de proveedores y contratos con HCPs.
* Creación de códigos en sistema para gestión del portafolio de productos.
* Apoyo en la gestión y segumiento de eventos de la unidad de negocio.
* Apoyo en los procesos administrativos y de reporte de la unidad de negocio (transferencias de valor, legalizaciones, entre otros).
Cualificaciones / Requisitos:
* Formación académica: Estudiante de carreras técnicas o tecnológicas en áreas administrativas (mercadeo, gestión administrativa, contabilidad, ingeniería industrial o afines).
* Manejo intermedio de herramientas de Office ...
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Type: Permanent Location: Bogotá Distrito Capital, CO-DC
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:08
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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:
Supply Chain Planning
Job Sub Function:
Production Planning & Scheduling
Job Category:
Professional
All Job Posting Locations:
Leiden, Netherlands
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 a Senior Detailed Scheduler to be in Leiden.
Purpose:
The Snr detailed scheduler is responsible for updating and maintaining the actual production schedule within the appropriate scheduling horizon (segment dependent) in local scheduling tools and handling process orders as per schedule.
Ensuring an optimized production schedule for the products, lines and site run in accordance with the latest customer demands and available capacity as well as downstream replenishment requirement.
You will be responsible for:
* Conversion of the Master Production Schedule (MPS) to the detailed day-to-day production schedule
* Optimize production schedules according to MPS, Operational Demands and available capacity.
* Assist in the development of medium-term plans to support scenario analysis, conflict analysis and production schedule business decisions.
* Provide planning support to the operations team for all Operations planning related aspects.
* Assist the Operations Team Lead in the coordination of Operations activities & respond to changes in demand.
* Act as the key point of contact for all functional areas to acquire critical planning information required to update and progress operations plans e.g.
Validation, maintenance, engineering, etc.
* Promote an environment to implement planning improvements in line with site strategies, get alignment on the MPS and incorporate the feedback on projects into production plans.
* Facilitate daily operations team meetings & weekly supply review meetings.
* Perform monthly resource forecasting, in conjunction with Operations Team Leads.
* Communicate the production plan across the operations areas, identifying any production and/or material constraint that can impact production progress.
Work with ...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:06
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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:
Customer Management
Job Sub Function:
Non-Technical Customer Service
Job Category:
Professional
All Job Posting Locations:
North Ryde, New South Wales, Australia
Job Description:
* Great Place to Work® Certified - 2024
* Competitive salary package, flexible work practices, award winning benefits
* Continuous training and development
ABOUT THE COMPANY
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
THE OPPORTUNITY
We are seeking a Supply Chain Enablement Lead to join Johnson & Johnson MedTech.
This is a unique opportunity to leverage your expertise in supply chain management to drive business growth and improvement.
As a Supply Chain Enablement Lead, you will be responsible for developing and implementing strategic supply chain initiatives that enhance customer experience, reduce costs, and improve operational efficiency.
If you are a motivated and results-driven professional looking to make a meaningful impact in the healthcare industry, we encourage you to apply for this exciting opportunity.
RESPONSIBILITIES
* Conduct ongoing gap assessment of critical metrics that matter for performance against capabilities through data reporting like Delivery Service Excellence (DSE) for customer experience contributed by broader functions within Supply Chain.
* The Supply Chain Enablement lead will coordinate the ongoing management and related activities for current EDI enabled customers as well as new onboarding activities.
* Identify root cause analysis and process improvement opportunities and work with key individuals/teams to implement actions to drive required changes
* Manage external client relationships, including contracts, statements of work (SOW), and purchase order processing for all activities related to EDI
* Provide and monitor key metrics, including Delivery Service Excellence, and coo...
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Type: Permanent Location: North Ryde, AU-NSW
Salary / Rate: Not Specified
Posted: 2025-04-02 08:16:03
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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:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
US004 PA Malvern - 200 Great Valley Pkwy
Job Description:
Johnson & Johnson Innovative Medicine, a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance Associate III to support Quality Operations.
This position will be located in Malvern, PA.
At Johnson & Johnson Innovative Medicine, we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We are Johnson & Johnson.
We collaborate with the world for the health of everyone in it.
Position Summary:
In this role, you will be responsible for providing quality oversight of the GMP Cell Banking Center of Excellence and affiliated laboratories including the cryofreezer storage room located at the Great Valley Parkway in Malvern, PA. Additionally, you will be responsible for quality support of the QC Cell Banking laboratories at the Phoenixville Pike location in Malvern, PA.
Primary responsibilities will include but are not limited to the Quality oversight of the production, testing, inventory, and supply of Master, Working, and Development Cell Banks for clinical, and commercial production as well as analytical testing for J&J biopharmaceutical and cell therapy products. The candidate will act as a liaison with other internal and external quality organizations to standardize policies, practices, and procedures to increase quality and compliance and champion increased awareness of quality related concerns.
This position will also help guide the quality strategy to support the pipeline of cell banking testing and release requirements.
Main responsibilities will include, but are not limited to:
* Partner with Cell Banking GMP Operations team to provide Quality oversight to successfully manufacture cell line products and support processes in the cGMP facility.
* Perform on the floor or desktop review of executed batch records and production documentation in support of batch release activities. Provide guidance with real time manufacturing and/or documentation discrepancies.
* Review and approve controlled documents including standard operating procedures, master batch records, test reports, COAs, work instructions, cell bank ...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:39
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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:
Legal & Compliance
Job Sub Function:
Enterprise Compliance
Job Category:
Professional
All Job Posting Locations:
New Brunswick, New Jersey, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for a Senior Manager, Privacy –MedTech Americas to be located in New Brunswick, NJ. Remote work options may be considered on a case-by-case basis and if approved by the Company.
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.
Purpose: The Senior Manager, Privacy, reporting directly into the Director, US MedTech Americas, will support the Privacy Compliance Program for designated Johnson & Johnson MedTech operating companies in the Americas.
The position is located in the United States but will participate in regional and global projects on a regular basis.
They will serve as strategic business partners for multiple operating companies in the United States and coordinate some cross-departmental activities, as advised by Global Privacy leadership, from time to time.
You will be responsible for:
* Establish and maintain key business, legal and IT relationships representing the Global Privacy function to the business for the sector and business operations assigned to the Sr.
Manager.
* Address new and evolving external legal and regulatory requirements.
* Ensure privacy risks are effectively identified and addressed by applying privacy by design principles, addressing training needs and providing compliance guidance.
* Preparation for internal and external Privacy compliance audits and supporting the organization with the implementation of corrective action solutions.
* Present and actively participate in compliance committees; support the Director MedTech Americas with preparing for presenting to leadership teams or similar governance councils.
* Collaborate with global/regional Privacy compliance community to share approaches to Privacy compliance and serve on teams to harmonize and optimize company approaches to Privacy.
* Participate in testing and monitoring program opportunities to demonstrate the Privacy compliance program is effective.
* Support other ...
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Type: Permanent Location: West Chester, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:39
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Als Senior Resolutions Generalist:in bist du verantwortlich für ein hervorragenden Remote-Kundenerlebnisses; Maximierung der Kundenzufriedenheit durch Bereitstellung der bestmöglichen Lösungen für komplexe Resolutions-Fälle (z.
B.
in Zusammenhang mit einem komplexen Sortiment oder komplexen Eskalationsverfahren), stets mit Empathie, Verständnis für die Kundenbedürfnisse und mit der Entschlossenheit, den Kund:innen einen besseren Alltag zu bereiten.
- Bereitstellung von qualitativ hochwertigem Kundensupport in allen Remote-Kanälen, um ein erstklassiges Kundenerlebnis zu schaffen und Vertrauen in die IKEA Marke aufzubauen
- Bereitstellung von Fachwissen zu bestimmten Sortiments- oder Servicebereichen, um die besten Lösungen für die Kund:innen zu finden
- Bereitstellung von Remote-Kundensupport bei komplexen und/oder eskalierten Resolutions-Fällen, wobei stets rechtliche Aspekte, die IKEA Policies und die Kundenzufriedenheit berücksichtigt werden, um eine angemessene Lösung zu finden
- Anwendung geeigneter Konfliktmanagementtechniken im Kundenkontakt, um zu reibungslosen und positiven Interaktionen beizutragen, die die Kundenbindung fördern
- Abgabe von Feedback über erforderliche Datenoptimierungen; Übernahme von Mitverantwortung dafür, dass alle Mitarbeitenden über das erforderliche Wissen verfügen, um die Bedürfnisse der Kund:innen zu erfüllen
Unser Ziel ist es unseren Kund:innen zu begegnen, wo und wann sie wollen! Egal ob über Telefon, Mail, Chat oder soziale Medien, wir finden immer die besten Lösungen für alle Anliegen von Informations- und Serviceanfragen, Reklamationen bis hin zum aktiven Verkauf.
Durch den tollen Support bei allen Interaktionen können wir langfristig Vertrauen und Treue zu unseren Kunden aufbauen und verbessern.
Deshalb suchen wir Allroundtalente! Bist du eines?
• Du hast Freude daran Probleme (Küchenreklamationen) in Luft aufzulösen und behältst so gut wie immer einen kühlen Kopf.
• Du bist neuen Medien gegenüber aufgeschlossen und arbeitest gern mit verschiedenen Tools.
• Du kommunizierst gern und gut: egal ob Telefon, Mail, Chat oder Soziale Medien.
• Du hast sehr gute Deutsch- und Englischkenntnisse.
• Du interessierst dich für Einrichtung, Trends und das Leben der Menschen zu Hause.
• Du bist flexibel, freust dich über Abwechslung bei den Arbeitszeiten und bist offen für Neues.
SMÅRT für dein Konto:
Unser monatliches Brutto-Mindestgehalt beträgt 2.380.- EUR auf Vollzeitbasis.
Dein tatsächliches Gehalt legen wir gemeinsam entsprechend deiner Qualifikation und Erfahrung fest.
Deine Benefits:
• Ein sicherer Arbeitsplatz mit einem Einstiegsgehalt über dem Kollektivvertrag in einem inklusiven und werteorientierten Unternehmen
• ONE IKEA Bonus - jährlich bei Zielerreichung für alle Mitarbeiter:innen
• Ein Dienstplan, abgestimmt auf deine Bedürfnisse, 4 Wochen im Vorhinein
• Weiterbildungs- und Aufstiegsmöglichkeiten im In- und Ausland
• Lebens- und private Unfallversicherung
• 15% Einkaufsrabatt und vergünstigtes Essen
Arbeitszeiten: Planbare Anwesenheiten innerhalb unserer Öffnungszeiten - Du bekommst deinen Dienstplan mind.
einen Monat im Voraus und hast die Möglichkeit zum Teil auch im Home Office zu arbeiten.
Wir freuen uns ausdrücklich über Bewerbungen von Menschen mit Behinderungen als auch mit verschiedenen ethnischen Hintergründen.
Gut zu wissen: Unser Auswahlprozess startet schon vor Ablauf der Bewerbungsfrist.
Sobald wir geeignete Personen gefunden haben, schließen wir den Auswahlprozess ab.
...
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Type: Permanent Location: Vösendorf, AT-3
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:37
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• Du berätst und betreust unsere Kund:innen in der Abteilung Schlafzimmer oder Wohnzimmer.
• Du gehst aktiv auf Kund:innen zu und zeigst ihnen kreative und funktionale Einrichtungslösungen für ihr Zuhause.
• Du hilfst unseren Kund:innen auch bei passenden Serviceleistungen – von der Lieferung bis zur Montage.
• Du sorgst dafür, dass dein Verantwortungsbereich sauber, aufgeräumt und mit Preisen versehen ist.
• Du hast Freude im Umgang mit Menschen.
• Du hast bereits Verkaufserfahrung gesammelt – ideal.
Genauso freuen wir uns über motivierte Quereinsteiger:innen, die gerne Neues lernen und ausprobieren möchten.
• Gemeinsames Arbeiten in einem Team ist genau dein Ding.
• Du bist an Einrichtung und am alltäglichen Leben der Menschen zu Hause interessiert.
• Du packst gerne mit an und bist körperlich belastbar.
SMÅRT für dein Konto:
Das Mindestentgelt für diese Position beträgt auf Basis einer Vollzeitbeschäftigung (38,5 Wochenstunden) € 2.380,- brutto pro Monat.
Diese Stelle wird geringfügig mit 8 Wochenstunden samstags besetzt, das entspricht einem monatlichen Bruttoentgelt von € 494,55.
Deine Arbeitszeiten: jeden Samstag laut Dienstplan.
Deine Benefits:
• Ein sicherer Arbeitsplatz mit einem Einstiegsgehalt über dem Kollektivvertrag in einem inklusiven und werteorientierten Unternehmen
• ONE IKEA Bonus (jährlich bei Zielerreichung für alle Mitarbeiter:innen)
• Ein Dienstplan, abgestimmt auf deine Bedürfnisse, 4 Wochen im Vorhinein
• Weiterbildungs- und Aufstiegsmöglichkeiten im In- und Ausland
• Lebens- und private Unfallversicherung
• 15% Einkaufsrabatt und vergünstigtes Essen
weitere Vorteile findest du auf IKEA.at/Jobs
SEI SMÅRT GANZ DU SELBST: WIR GLAUBEN AN KARRIERE OHNE BARRIERE
In Schubladen denken wir nur, wenn es um Kommoden geht.
Deshalb setzen wir auf die Förderung von Geschlechtergerechtigkeit, einen bunten Mix aus Generationen, die Inklusion von Personen mit Behinderungen und einen offenen Umgang mit Religion, Glaube und Weltanschauung.
Mehr zu Inklusion, Vielfalt und Gleichheit bei IKEA findest du unter:Inklusion, Vielfalt & Gleichheit am Arbeitsplatz - IKEA Österreich
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Type: Permanent Location: Salzburg, AT-5
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:32
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description:
We are searching for the best talent for a Manager, Global Regulatory Affairs, Established Products to be in Warsaw, Poland.
This position follows a hybrid working model
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
Key Responsibilities:
The Regulatory Scientist provides support to the Global Regulatory Leader (GRL) for regulatory activities in the assigned portfolio, including assuring that content of regulatory filings support our global regulatory strategy and product strategy position.
Input in development, post-approval and life cycle management
* Participate in global regulatory team meetings as appropriate
* Advise the regulatory team on applicable regulatory requirements, project specific regulatory issues as assigned
* Supporting late life cycle compliance activities, divestment and delisting
* Develop an understanding of the global regulatory environment, competitor intelligence and Established Products portfolio
Liaison with Regulatory Agencies and Local Operating Companies
* Act as back-up for contact with Regulatory Agencies as needed
* Draft cover letters for Regulatory Agency communication
* Assist in the preparation of meetings with Regulatory Agencies
* Liaise with LOCs, and ensure responses to queries are made in timely manner, and that content is consistent with the regulatory strategy.
Input in process development
* Assist in development and improvement of processes related to regulatory submissions;
Clinical Trials
* Review clinical trial plans and protocols and ensure alignment with regulatory requirements;
Health Authority Submissions (e.g.
Briefing Books, Scientific advice packages, Marketing Authorization Applications (MAAs), New Drug Applications (NDAs) or equivalent regional or national documents)
* Provide regulatory support throughout registration process an...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:30
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
US121 NJ Raritan - 1000 Highway 202 S
Job Description:
Ethicon, part of the Johnson & Johnson Family of Companies, is recruiting a Global Supply Chain Planning Co-Op to join the External Manufacturing Planning team.
At Ethicon, our measure of success is the people we impact around the world - the patients who are now enjoying longer, healthier and more fulfilling lives.
We’re committed to addressing the world’s most pressing healthcare issues by advancing technologies, research and training, and working with healthcare providers globally to create solutions that improve health outcomes and expand access to quality surgical care.
From creating the first sutures to revolutionizing surgery with minimally invasive procedures to finding innovative solutions today, Ethicon has been shaping the future of surgery for more than 100 years.
As an integral member of Ethicon’s Supply Chain Planning Team, you will have the opportunity to play a key role in ensuring that our patients and doctors are getting the surgical devices they need when they need them.
DUTIES & RESPONSIBILITIES
Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Conduct all planning activities for one of Ethicon’s external manufacturers
* Develop detailed supply plans that will be used to coordinate production at the external manufacturer
* Own the end-to-end Order Management process, including placing new purchase orders, developing purchase forecasts, and performing virtual receipts
* Identify and escalate product vulnerabilities to cross-functional business partners and stakeholders
* Improve capabilities and effectiveness of the Sales & Operations Planning process
* Monitor and report on key performance metrics, while offering insights and suggestions on how to improve the business
* Be empowered to design and implement improvements to new and existing processes that will benefit the Planning team and broader organization
* Become a team Subject Matter Expert for multiple ERP systems, including SAP and JD Edwards
* Utilize various Data Visualization and Analytics tools such as Tableau and SQL to own and execute critical reports and dashboards f...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:27
-
• Du befüllst gemeinsam mit deinen Kollegen:innen die Regale in der Markthalle oder Selbstbedienungshalle und bei den Zusatzverkaufsplätzen.
• Du entsorgst Verpackungsmaterial und kümmerst dich um die Mülltrennung.
• Du verschlichtest die Retourware, befüllst die Verkaufsfächer und sorgst für Ordnung und Sauberkeit.
• Du bist körperlich belastbar und hast Lust darauf, kräftig mit anzupacken.
• Schnelles und genaues Arbeiten ist für dich selbstverständlich.
• Du nutzt den Tag schon gerne in den Morgenstunden.
• Arbeiten Hand in Hand mit deinem Team ist genau dein Ding.
SMÅRT für dein Konto:
Das Mindestentgelt für diese Position beträgt auf Basis einer Vollzeitbeschäftigung (38,5 Wochenstunden) € 2.380,- brutto pro Monat.
Diese Stelle wird in Teilzeit mit 25 Wochenstunden besetzt, das entspricht einem monatlichen Bruttoentgelt von € 1.545.
Deine Arbeitszeiten: 4-9 Uhr morgens von Montag bis Samstag an 5 Tagen pro Woche - jeden Samstag (ein Tag zw.
Mo-Fr frei).
Deine Benefits:
• Ein sicherer Arbeitsplatz mit einem Einstiegsgehalt über dem Kollektivvertrag in einem inklusiven und werteorientierten Unternehmen
• ONE IKEA Bonus (jährlich bei Zielerreichung für alle Mitarbeiter:innen)
• Ein Dienstplan, abgestimmt auf deine Bedürfnisse, 4 Wochen im Vorhinein
• Weiterbildungs- und Aufstiegsmöglichkeiten im In- und Ausland
• Lebens- und private Unfallversicherung
• 15% Einkaufsrabatt und vergünstigtes Essen
weitere Vorteile findest du auf IKEA.at/Jobs
SEI SMÅRT GANZ DU SELBST: WIR GLAUBEN AN KARRIERE OHNE BARRIERE
In Schubladen denken wir nur, wenn es um Kommoden geht.
Deshalb setzen wir auf die Förderung von Geschlechtergerechtigkeit, einen bunten Mix aus Generationen, die Inklusion von Personen mit Behinderungen und einen offenen Umgang mit Religion, Glaube und Weltanschauung.
Mehr zu Inklusion, Vielfalt und Gleichheit bei IKEA findest du unter:
....Read more...
Type: Permanent Location: Vösendorf, AT-3
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:23
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
CO015 One JNJ Bogota Building
Job Description:
En Johnson & Johnson, la compañía del cuidado de la salud más grande del mundo, nos unimos con un propósito: transformar la historia de la salud humana.
La diversidad y la inclusión son esenciales para continuar construyendo sobre nuestra historia de liderazgo e innovación, que ha tenido un impacto en la salud de más de mil millones de pacientes y consumidores todos los días durante más de 130 años.
Independientemente de su raza, credo, orientación sexual, religión o cualquier otro rasgo, TU eres bienvenido para todos los puestos
vacantes en la compañía de atención médica más grande del mundo.
Cuando se una a Johnson & Johnson, su adición a la compañia podría significar nuestro próximo gran avance.
Por eso abrimos nuestras puertas para recibirte y juntos escribamos el siguiente paso de nuestra historia en el Programa de Aprendices.
Nuestro programa tiene como objetivo atraer y contratar talentos como TÚ, que actualmente estén cursando carreras técnicas y tecnológicas, que busquen aprender durante su etapa productiva y tengan la mejor actitud para asumir grandes desafios.
Propósito:
El aprendiz del SENA que se incorpore al área de recursos humanos desempeñará funciones esenciales para el buen manejo administrativo de los recursos humanos.
A continuación, se detallan los requerimientos necesarios para cumplir con estas funciones de manera efectiva.
Principales Responsabilidades:
* Generar reportes y hacer seguimiento a la ejecución de los procesos del área asignada.
* Brindar soporte al proceso de comunicaciones del área.
* Digitalizar y administrar los archivos del área (digital y físico).
* Manejar el software, las herramientas del área, y las bases de datos.
* Realización de impresiones y archivo de documentos relevantes para el departamento.
* Apoyo en la gestión de pagos de empleados del SENA, asegurando la correcta presentación y tramitación de la información.
Qualifications - External
Requisitos:
* Formación académica: Estudiante de carreras técnicas o tecnológicas en áreas administrativas (mercadeo, gestión administrativa, contabilidad, ingeniería industrial o afines).
El estudiante debe tener disponibilidad para realizar su etap...
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Type: Permanent Location: Bogotá Distrito Capital, CO-DC
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:22
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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. Every role within Adare offers you a unique, customized experience with a chance to make a real impact that 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 as per internal agreement
* Career growth and internal opportunities
* Performance/production bonus
* Employee Recognition Programs.
We are seeking to hire a Manager, Quality Assurance Operations & QP to join our Italian QUALITY TEAM at Pessano con Bornago.
If any of the below describes you, we would love to meet you!
Job Summary
The Manager, Quality Assurance Ops acts as lead for the QA Operation group and carries out and covers the following responsibilities:
* Manages the QA Specialist/Sr Specialist group of the site for the deviation/ investigation , Batch Record reviews and release functions and ensures their correct training and professional growth
* Manages the QA Specialist/Sr Specialist quality on the floor of the site for the oversight of production activities
* Is the first point of contact with customer relating deviation, CAPA and complaints
* Acts as a Qualified Person at Pessano site
* Supervise and verify that each batch of medicine is produced and controlled by preparing all the necessary operations and measures to allow the aforementioned controls to be carried out
* Is responsible for managing the documentation relating to the production and controls of the products and its availability
* Ensure the management of narcotic and psychotropic substances and drug precursors
* Identifies areas and activities for improvement from a procedural point of view, promotes the drafting of the Standard Operating Procedures and their approval and application
* Manages the personnel who deal with the deviations and non-conformities found, ensuring the quality of the outgoing product and verifying the effectiveness of the corrective actions taken
* Manages the personnel who deal with customer complaints with related investigation, corrective activities, response and closure of complaints
* Works cooperatively with managers, supervisors, collaborators, customers and the public
* Complies with the policies, procedures and regulations in force in the company.
Required Skills and Qualifications
* Master's Degree in Scientific Disciplines: Chemistry and Pharmaceutical Technology (CTF ), Biological Sciences , Pharmacy or similar
...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:15
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At ERM we are committed to supporting our private markets investor clients as they look to decarbonize their portfolio companies and drive growth via sustainability value creation levers.
Our private markets value creation team is currently going through a period of significant growth in the market while also servicing an existing large base private equity and infrastructure investor clients. Consultants in the Private Markets value creation team work on a wide range of interesting strategic and operational projects at portfolio company level for private markets investor clients.
This person will partner across ERM’s industry teams and lines of business to develop innovative sutainability & decarbonization solutions that meet the needs of both portfolio companies and General Partner goals, investment outcomes and programs.
The incoming consultant will be expected to deliver projects and build relationships with current and new clients in the private markets investor space.
As a consultant, you will manage projects, motivate staff at all levels and contribute to the achievement of ERM’s delivery of sustainability & decarbonization strategy development and implementation projects.
ERM has enduring values, which are fundamental to our business conduct.
We are passionate about our people, their safety, well-being and development.
ERMers take accountability, are client-focused, and collaborate with colleagues across geographies.
If you share our values, believe in sustainability and are motivated by opportunities to shape, build and run a sustainability service team that makes a real impact to our private markets investor client’s businesses, ERM is the right place for you.
As a project manager in your industry you have developed an in-depth knowledge of private equity and infrastructure investors and portfolio operations teams.
You have experience supporting and leading strategic engagements at the C-suite level and partnering, guiding & educating senior management teams on interpreting and creating action plans around the development of strategy & quantified implementation roadmaps and setting credible financial targets from sustainability & decarbonization projects.
You will have a deep understanding of commercial and operational value creation levers, corporate strategy, market sizing, operational efficiency measures, low carbon solutions, industrial decarbonization, and sustainable value chain initiatives.
You have prior experience managing and successfully delivering corporate strategy programs for mid-market companies and have an understanding of how those operational projects fit within private equity and infrastructure clients’ sustainability & decarbonization programs, targets, and broader investment processes as well as energy transition & impact fund investor needs.
You enjoy building, coaching, and mentoring collaborative teams as part of a large global business.
This role will work across ERM and the firm’s sustainabili...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-02 08:15:07
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Your Job
Georgia-Pacific is now hiring for Relief Equipment Operators for our lumber mill in Gurdon, Arkansas.
This is a production position responsible for operating various machinery such as edgers, trimmers, and other related equipment to process logs into lumber.
A strong commitment to safety is critical for success in this role.
If you thrive in a fast-paced environment and have a strong commitment to safety standards with lumber processing experience, this may be the role for you!
Pay rate is $23.00 per hour.
Must be open to day shift or night shift schedule.
Night shift differential is an additional $1.50 per hour.
Our Team
Georgia-Pacific employees strive for safety and health excellence while achieving an injury free workplace.
To learn more about our Building Products division, visit http://www.buildgp.com .
What You Will Do
* Operate equipment to defined standards and product specification targets
* Adhere to all plant safety and environmental guidelines, policies, and procedures
* Work collaboratively with other team members
* Conduct required quality checks on products to ensure customer satisfaction
* Complete appropriate reporting at the end of each day
* Work at elevated heights and in close cab quarters
* Must be able to work any shift, holidays, weekends, and overtime as needed
* Be willing to work in a hot, humid, cold, and noisy industrial environment
Who You Are (Basic Qualifications)
* At least six (6) months of experience operating log processing equipment
What Will Put You Ahead
* High School Diploma or GED
* At least one (1) year of experience operating log processing equipment
* Knowledge of lumber length and dimensions
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, specialty fibers, building products and much more, Georgia-Pacific works to meet evolving needs of customers worldwide with quality products.
In addition to the products we make, we operate one of the largest recycling businesses.
Our more than 30,000 employees in over 150 locations are empowered to innovate every day - to make everyday products even better.
At Koch, employees...
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Type: Permanent Location: Gurdon, US-AR
Salary / Rate: Not Specified
Posted: 2025-04-02 08:12:11
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Georgia-Pacific is now hiring a Production Supervisor at our Sheboygan, WI Facility.
The Supervisor will utilize leadership, operations experience, and communication to identify and drive improvement opportunities related to people, process, and systems.
The ideal candidate will demonstrate safety as a value and lead a crew of employees to exceed production expectations for the shift.
The candidate must be self-driven and demonstrate a commitment to safety, manufacturing excellence and quality.
Will also possess strong interpersonal communication and technical skills as well as being capable of leading transformation initiatives.
Opening currently available:
Converting - 2 nd shift - 3:00pm - 11:00pm
Our Team
Georgia-Pacific is one of the nation's leading corrugated box manufacturers.
Understanding customer needs and providing creative and custom solutions makes Georgia-Pacific much more than a typical corrugated packaging supplier and partner.
The team at Sheboygan specializes in the Bulk Box Making Process with both converting and corrugator assets, where they support the self-actualization of their employees.
This position provides opportunities for promotion both in Sheboygan as well as many other Georgia-Pacific and Koch facilities across the country.
Come join our team!
To learn more about this facility and our Packaging division, please visit:
Georgia-Pacific: How Corrugated Boxes are Made
Georgia-Pacific: Corrugated
www.gppackaging.com
What You Will Do
* Lead an operating team in compliance in safety, health, environmental, and quality
* Drive safety excellence through promoting employee involvement, ownership, and accountability to proactively identify hazards and implement appropriate mitigating strategies; investigate incidents and participate in resolution of causes
* Coach, train, and develop operations personnel in safety, quality, and production
* Ensure best practices are followed for minimization of waste at machine centers
* Address key issues and concerns and interact with employees from other departments to ensure quality, on-time production
* Plan, assign and direct work for all hourly production employees; appraise performance and provide feedback as needed; assist in resolving complaints; hold employees accountable as needed; communicate issues and results on a daily basis
Who You Are (Basic Qualifications)
* Experience working in the corrugated packaging/containerboard industry on a corrugator OR in a converting operation
* Previous experience supervising employees within a manufacturing, production, industrial OR military environment
* Must have legal authorization to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship
What Will Put You Ahead
* Bachelor's degree or higher
* Experience working with KIWI application
At Koch companies, we are entrepreneurs.
This means we openly challenge the status qu...
....Read more...
Type: Permanent Location: Sheboygan, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-02 08:12:11
