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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: 2025-06-21 08:20:35
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ERM is seeking a motivated Consulting Associate, Air Quality to join our consulting team in our Indianapolis, Indiana office.
The successful candidate will work on a variety of interesting technical projects for clients in the technology, energy, and manufacturing sectors throughout the Midwest.
This is an excellent career opportunity to work with an expert consulting team on challenging environmental management projects for large industrial and global clients.
Access to ERM's national Air Quality & Climate Change experts provide knowledge sharing of best practices across the industry and ongoing learning opportunities for our team.
ERM’s Air Quality & Climate Change technical community pursues and wins highly innovative engagements for the most interesting clients, providing the full breadth of air quality and climate change services.
With annual global sales in excess of $50 million, ERM’s Air Quality & Climate Change service area is one of the largest among its peers in our industry and is steadily growing at a double-digit pace.
In North America alone, ERM has more than 300 dedicated air quality and climate change professionals assisting clients with projects as diverse as facility and process permitting, developing responses and approaches to support emerging Low Carbon Economy Transition issues, to leading complex capital projects through the many hurdles associated with the New Source Review (NSR) permitting program.
RESPONSIBILITIES:
* Conduct air quality analyses, assess regulatory compliance, and perform regulatory applicability evaluations.
* Develop complete and accurate air quality permit applications/documentation for Title V, PSD, and NSR compliance.
Interact with local regulators to steward permit application review and issuance.
* Prepare emission inventory reports (criteria and GHG); quantify air pollutant emissions and impacts, and complete toxic release inventory (TRI) reporting.
* Evaluate air pollution control technologies, including technical and economic feasibility of air pollution control equipment.
* Implement climate change projects, such as greenhouse gas inventories, emission reductions, energy efficiency, public disclosure and verification.
* Assist clients with MACT compliance programs.
* Implement environmental compliance management systems and processes.
* Prepare recommendations and reporting of results.
* Perform environmental compliance audits and implement follow-up corrective actions to ensure compliance with federal, state, and local regulations.
* Perform multiple tasks within scope/budget/schedule expectations and ensure quality standards on project deliverables.
* Interact and maintain successful relationships with clients, ERM employees, and subcontractors.
REQUIREMENTS:
* BS in chemical, environmental, or mechanical engineering or related degree; MS preferred.
Non-engineering degrees will be considered with relevant experience.
Or eq...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-06-21 08:17:26
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
At Elanco (NYCE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Elanco Animal Health ist eines der weltweit führenden Tiergesundheitsunternehmen.
Wir entwickeln und vertreiben innovative Produkte und Dienstleistungen, um Krankheiten bei Haus- und Nutztieren vorzubeugen und zu behandeln.
So schaffen wir einen Mehrwert für Landwirte, Haustierbesitzer, Tierärzte, Stakeholder und die gesamte Gesellschaft.
Mit unserer langjährigen Tradition im Bereich Tiergesundheit helfen wir unseren Kunden dabei, die Gesundheit ihrer Tiere zu erhalten und zu verbessern.
Die Lohmann Animal Health GmbH ist als Teil des Elanco Animal Health Unternehmens seit mehr als 50 Jahren ein weltweit führender Spezialist für die Herstellung von Geflügelimpfstoffen.
Unsere Impfstoffe werden dabei weltweit in über 70 Ländern exportiert.
Join our team!
Wir suchen Sie, zum nächstmöglichen Termin als neue/n Produktionsmitarbeiter (m/w/d) für unsere Teams!
IHRE AUFGABEN UND VERANTWORTLICHKEITEN
· Mitarbeit bei der Herstellung von unseren viralen/bakteriellen Impfstoffen
· Selbständiges Bedienen, Einrichten und Überwachen von Produktionsanlagen
· Gewährleistung eines reibungslosen Produktionsablaufs sowie Dokumentati...
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Type: Permanent Location: Cuxhaven, DE-NI
Salary / Rate: 3659
Posted: 2025-06-20 08:46:56
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Sr.
Analytical Scientist, Biologics
As an Sr.
Analytical Scientist, Biologics you will be part of Elanco’s R&D team, driving the development of chromatographic, electrophoretic, and LC/MS analytical methods for biopharmaceutical products.
In this role, you’ll be responsible for advancing analytical techniques for therapeutic proteins and vaccines, supporting bioprocesses, and leading method development, validation, and transfer efforts across global sites.
If you are passionate about advancing analytical methodologies and playing a key role in biopharmaceutical development, we invite you to apply and join our innovative team!
Your Responsibilities:
* Develop and optimize chromatographic, electrophoretic, and LC/MS analytical methods for vaccine and therapeutic protein products.
* Innovate and implement analytical solutions for diverse drug formulations and bioprocess support.
* Lead method validation, verification, and transfer activities across global sites and CROs.
* Train and mentor associates and scientists globally to ensure consistency in analytical practices.
* Author technical reports, review scientific documents, and maintain laboratory safety standards.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s Degree with 12+ years or Master’s Degree with 10+ years of experience in Analytical Chemistry, Biochemistry, Biophysics, or a related scientific field.
* Experience: Extensive hands-on experience developing HPLC/UPLC-based, electrophoretic, and LC/MS analytical methods for large molecule characterization.
* Top 2 skills: Strong expertise in analytical method development and validation, with excellent problem-solving and communication skills.
What will give you a competitive edge (preferred qualifications):
* Expertise in recombinant proteins, monoclonal antibodies, oligonucleotides, and peptides.
* Experience with method validation, transfer, and qualification under GMP conditions.
* Strong statistical knowledge and proficiency with statistica...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 123500
Posted: 2025-06-20 08:46:49
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Harris Computer, the largest operating group of Constellation Software Inc.
(TSX:CSU), is looking for a Corporate Development Specialist based in the USA or Canada to join our expanding team of talented corporate development professionals on the mergers and acquisitions (M&A) team.
This team works closely with Harris’s senior management in continuing the company’s success in acquiring software businesses.
What your impact will be:
* Directly engage the decision makers at software businesses to identify, maintain and nurture acquisition opportunities for Harris, using a suite of communication and customer relationship management tools.
* Continue relationships with our existing network of acquisition targets.
* Become the senior account manager of Harris’ M&A relationships in your area of coverage.
* Effectively communicate Harris’ investment strategy, while ensuring that the investment process is handled with care and professionalism.
* Support the M&A team in qualifying potential company targets.
* Track activities and maintain relevant information in Salesforce.
* Generate and report on leads, set up qualified investment opportunities and move opportunities through the M&A pipeline to our M&A transactions team.
What we are looking for:
* 5+ years of related business experience.
Sales, corporate development, consulting, banking, investing, M&A sourcing, technology/software, investor relations, or entrepreneurship/start-up experience are all considered valuable experience and will be highly considered
* Aptitude and passion for corporate development and relationship management
* Exceptional people skills, organizational, written, and verbal communication skills
* Self-starter with excellent prioritization and multi-tasking abilities who thrives on new challenges and takes initiative
* Experimentation is part of what we do at Harris.
All candidates will be considered, if you think you may be a good fit for the role, we want to hear from you
What we can offer:
* Attractive compensation package consisting of base salary, quarterly and annual variable bonus incentives.
* Comprehensive Medical, Dental and Vision coverage from your first day of employment.
* Flexible, remote work.
*Only successful candidates will be contacted
*.
Harris is an Equal Opportunity Employer and members of the following targeted groups are encouraged to apply women, persons with disabilities, aboriginal peoples and visible minorities.
If you are a person with a disability, assistance with the screening and selection process is available on request.
The Harris Talent Acquisition team does not use text messages to contact candidates or solicit confidential information.
We encourage all candidates to apply for advertised positions.
They will be contacted either by a Harris manager or by a member of the Talent Acquisition team for an interview, once the required ...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-20 08:46:08
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Résumé du poste :
Nous recherchons un(e) Gestionnaire de Comptes Clients axé(e) sur la croissance commerciale pour développer et fidéliser un portefeuille de clients existants sur la plateforme Acumatica Cloud ERP.
Vous jouerez un rôle clé dans la réalisation des objectifs de vente en identifiant de nouvelles opportunités chez nos clients actuels, en gérant les renouvellements contractuels et en assurant un haut niveau de satisfaction client.
Votre capacité à créer de la valeur, à établir des relations de confiance et à faire évoluer les comptes stratégiques sera déterminante pour le succès de ce poste.
Responsabilités principales:
Développement des revenus
* Identifier de nouvelles opportunités commerciales (ex : upsell, cross-sell) au sein d’un portefeuille de clients existants.
* Négocier les contrats, les renouvellements et les extensions de services en vous appuyant sur la valeur business de nos solutions.
* Atteindre les objectifs de revenus mensuels et trimestriels tout en assurant la satisfaction client.
Fidélisation et relation client:
* Être le point de contact stratégique post-vente pour vos clients afin de maintenir une relation proactive et durable.
* Comprendre les enjeux technologiques, fonctionnels et opérationnels de chaque client afin de proposer des solutions pertinentes.
* Proposer des offres de services professionnels permettant de répondre aux besoins des clients.
Travailler en étroite collaboration avec les équipes opérationnelles afin de coordonner la réalisation des travaux dans le respect du cadre budgétaire en assurant la satisfaction client.
* Organiser des revues de compte régulières (QBR) pour assurer la continuité et maximiser l’adoption de nos solutions.
* Identifier les signaux d’alerte (ex : insatisfaction, sous-utilisation) et les adresser rapidement avec les équipes concernées.
Profil recherché:
* Expérience confirmée (3 à 5 ans) dans la gestion de comptes clients avec un volet commercial fort (B2B, solutions complexes, SaaS ou services).
* Solide capacité de vente, de négociation et d’identification d’opportunités de croissance chez les clients existants.
* Excellentes compétences relationnelles, sens de l’écoute, capacité à influencer et à convaincre.
* Esprit stratégique, orienté résultats, avec une forte autonomie.
Atouts supplémentaires:
* Expérience en vente consultative ou gestion de comptes stratégiques, particulièrement dans le secteur des services professionnels.
* Connaissance des cycles de vente long et/ou multi-interlocuteurs.
* Familiarité avec des solutions technologiques ou logicielles.
* Expérience CRM reporting, facilitant l’optimisation des processus de vente et de gestion de la relation client
Ce que nous offrons:
* Rémunération compétitive (base + commissions) alignée sur vos performances.
* Télétravail et ...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-06-20 08:46:05
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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.
Manpower est le chef de file mondial en matière de solutions d’emploi innovante.
Nous offrons des solutions qui ont un impact positif permettant à ces clients d’atteindre leurs objectifs d’affaires et être plus compétitif sur le marché.
En affaire depuis plus de 70 ans nos solutions englobent un ensemble de besoins qui ont comme dénominateur commun le TALENT, le RECRUTEMENT, GESTION DE CARRIÈRE , FORMATION.
Manpower saura contribuer à votre réussite dans cette ère ou le capital humain et les talents sont en constantes mutations.
Sous la supervision et en soutien du Gestionnaire de l’approvisionnement en Capital, le mandat principal de l'Assistant Achat est de participer à l'acquisition de biens et de services en optimisant la valeur du processus pour Alcoa (prix, qualité, coût total de propriété, etc.).
L’Assistant Achat sera également appelé à effectuer des recherches, des analyses, des négociations, le suivi et la mise en œuvre de contrats d'approvisionnement avec les fournisseurs.
En outre, il doit répondre efficacement aux différentes demandes de l'organisation et de ses clients internes.
Les principales responsabilités du poste comprennent :
Préparation des projets d’achat
* Participer au recueil des besoins, à la création des spécifications destinées aux fournisseurs
* Rédiger les comptes rendus des réunions de son équipe, et des réunions de clarifications.
* Préparer la phase de négociation de l’équipe : documenter des dossiers fournisseurs, relever des éléments d’argumentaire ou de vigilance.
* Gérer la gestion documentaire via Sharepoint de l’ensemble des documents achat.
Participation aux relations commerciales avec les fournisseurs
* Participer au sourcing : lancer des consultations d’offres via notre outil de sourcing (Ariba).
* Suivre et communiquer les évolutions des spécifications, demander des devis détaillés et chiffrés (RFQ request for quotation).
* Coordonner les visites fournisseurs sur site.
* Renseigner et documenter les matrices de comparaison.
Gestion administrative des commandes
* Suivre l’émission et la réception des bons de commande.
* Suivre les délais et la confirmation des livraison.
Reporting et saisie des dossiers fournisseurs
* Actualiser la base interne de données dédiées aux fournisseurs.
* Produire et mettre à jour les reporting et les tableaux de bord des activités avec les données des projets.
Ce que vous pouvez apporter au rôle :
* BAC dans une discipline connexe (administration, logistique, etc.).
Une formation collégiale DEC pourra être considérée si combinée à une expérience significative en lien avec le poste
* 2-3 ans d’expérience d...
....Read more...
Type: Permanent Location: Deschambault, CA-QC
Salary / Rate: Not Specified
Posted: 2025-06-20 08:44:21
-
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.
Manpower est le chef de file mondial en matière de solutions d’emploi innovante.
Nous offrons des solutions qui ont un impact positif permettant à ces clients d’atteindre leurs objectifs d’affaires et être plus compétitif sur le marché.
En affaire depuis plus de 70 ans nos solutions englobent un ensemble de besoins qui ont comme dénominateur commun le TALENT, le RECRUTEMENT, GESTION DE CARRIÈRE , FORMATION.
Manpower saura contribuer à votre réussite dans cette ère ou le capital humain et les talents sont en constantes mutations.
Sous la supervision et en soutien du Gestionnaire de l’approvisionnement en Capital, le mandat principal de l'Assistant Achat est de participer à l'acquisition de biens et de services en optimisant la valeur du processus pour Alcoa (prix, qualité, coût total de propriété, etc.).
L’Assistant Achat sera également appelé à effectuer des recherches, des analyses, des négociations, le suivi et la mise en œuvre de contrats d'approvisionnement avec les fournisseurs.
En outre, il doit répondre efficacement aux différentes demandes de l'organisation et de ses clients internes.
Les principales responsabilités du poste comprennent :
Préparation des projets d’achat
* Participer au recueil des besoins, à la création des spécifications destinées aux fournisseurs
* Rédiger les comptes rendus des réunions de son équipe, et des réunions de clarifications.
* Préparer la phase de négociation de l’équipe : documenter des dossiers fournisseurs, relever des éléments d’argumentaire ou de vigilance.
* Gérer la gestion documentaire via Sharepoint de l’ensemble des documents achat.
Participation aux relations commerciales avec les fournisseurs
* Participer au sourcing : lancer des consultations d’offres via notre outil de sourcing (Ariba).
* Suivre et communiquer les évolutions des spécifications, demander des devis détaillés et chiffrés (RFQ request for quotation).
* Coordonner les visites fournisseurs sur site.
* Renseigner et documenter les matrices de comparaison.
Gestion administrative des commandes
* Suivre l’émission et la réception des bons de commande.
* Suivre les délais et la confirmation des livraison.
Reporting et saisie des dossiers fournisseurs
* Actualiser la base interne de données dédiées aux fournisseurs.
* Produire et mettre à jour les reporting et les tableaux de bord des activités avec les données des projets.
Ce que vous pouvez apporter au rôle :
* BAC dans une discipline connexe (administration, logistique, etc.).
Une formation collégiale DEC pourra être considérée si combinée à une expérience significative en lien avec le poste
* 2-3 ans d’expérience d...
....Read more...
Type: Permanent Location: Bécancour, CA-QC
Salary / Rate: Not Specified
Posted: 2025-06-20 08:44:20
-
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.
Manpower est le chef de file mondial en matière de solutions d’emploi innovante.
Nous offrons des solutions qui ont un impact positif permettant à ces clients d’atteindre leurs objectifs d’affaires et être plus compétitif sur le marché.
En affaire depuis plus de 70 ans nos solutions englobent un ensemble de besoins qui ont comme dénominateur commun le TALENT, le RECRUTEMENT, GESTION DE CARRIÈRE , FORMATION.
Manpower saura contribuer à votre réussite dans cette ère ou le capital humain et les talents sont en constantes mutations.
Durée de 18 mois à temps plein.
Relevant du Superviseur d’exploitation SST, le titulaire du poste devra concevoir et actualiser les programmes d’hygiène industrielle en fonction des différents risques pouvant affecter les travailleurs.
Il proposera également des recommandations afin d’identifier, d’évaluer et de contrôler les risques pour la santé des travailleurs dans un environnement de production d’aluminium.
Il agit à titre d’expert technique en matière d’hygiène industriel et collabore étroitement avec les équipes de santé-sécurité, d’ingénierie, de production et les représentants syndicaux pour s’assurer du maintien d’un milieu de travail sain et sécuritaire.
Il est en charge de participer à la mise à jour du programme de santé de l’usine en collaboration avec divers partenaires internes (techniciens en hygiène, conseillers SST, équipe de santé et équipes de sureté industrielle de production et d’entretien).
Responsabilités Spécifique:
* Réaliser des évaluations des expositions professionnelles (poussières, fumées métalliques, gaz, bruits, rayonnement, vibrations, chaleur, solvants, ergonomie, etc.).
Proposer des mesures et des moyens permettant d'éliminer ou, à défaut, de réduire les risques et les dangers potentiels;
* Rédige des rapports techniques et formule des recommandations pratiques pour la réduction ou l’élimination des risques.
* Développer et mettre en œuvre des programmes de surveillance de l’environnement de travail.
Élabore les plans et stratégie d’échantillonnage annuel
* Assurer l’échantillonnage des travailleurs aux divers contaminants en veillant de suivre le plan d’échantillonnage établi;
* Assurer la conformité aux lois, règlements et aux normes applicables.
Demeure à l’affut des meilleures pratiques de l’industrie.
* Développer et diffuser les formations nécessaires auprès des employés;
* Effectuer les suivis d’avancement des mesures correctives et/ou plans d’actions;
* Maintenir la gestion des produits dangereux (suivi SIMDUT/SGH, Paratox);
* Effectuer des audits plancher (SIMDUT/SGH, protection respiratoire, protection aud...
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Type: Permanent Location: Becancour, CA-QC
Salary / Rate: Not Specified
Posted: 2025-06-20 08:44:19
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Plant Environment and Sustainability Leader (Paris, TX.)
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.
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, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business.
SUMMARY OF POSITION:
As a key contributor to the Environment & Sustainability (E&S) team, this role assumes a leadership position in driving Kimberly-Clark’s (K-C) commitment to Better Care for a Better World.
Serving as the Site Environmental Coordinator, the role provide leadership specifically for the environmental aspects of OH&S and E&S programs and systems, particularly at the company’s non-manufacturing locations.
The position ensures that the facility is strategically aligned and operating in conformance with K-C OH&S and E&S Standards and in compliance with local legal requirements.
Key Responsibilities:
* Legal Compliance Management: Monitor and manage the implications of relevant legal requirements applicable to site activities and operations.
* Risk Management: Effectively handle identified environmental risks.
* Subject Matter Expertise: Demonstrate competence in relevant environmental and sustainability topics, especially about topics addressed by K-C OH&S and E&S Perf.
Stds.
and associated operation-specific risks.
* Incident Support:...
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Type: Permanent Location: Paris, US-TX
Salary / Rate: Not Specified
Posted: 2025-06-20 08:43:41
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Plant Health & Safety Manager (Paris, TX.)
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.
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, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business.
SUMMARY OF POSITION:
As an integral part of the Occupational Health & Safety (OH&S) team, the Site Occupational Health & Safety Lead assumes a leadership position, spearheading Kimberly-Clark’s (K-C) commitment to Better Care for a Better World.
This role provides strategic leadership specifically for the occupational health and safety aspects of OH&S and E&S programs and systems, focusing on the company’s moderately complex locations.
The primary objective is to ensure strategic alignment with K-C OH&S and E&S Standards and compliance with local legal requirements.
Through influence without authority and/or direct reporting relationships, the position works collaboratively to identify and direct appropriate process and systems that elevate site program maturity, effectively manage risks, and deliver continuous improvement in occupational health and safety results. Site Health & Safety Lead may have local staff to assist in delivering on accountabilities and typically report to Mill/Site Managers.
Key Responsibilities:
* Legal Compliance Management: Interpret, understand, an...
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Type: Permanent Location: Paris, US-TX
Salary / Rate: Not Specified
Posted: 2025-06-20 08:43:41
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Georgia-Pacific is actively seeking an Product Compliance Manager-International for our Building Products Gypsum products.
This is an exciting opportunity for an individual who is passionate about product compliance and wants to make a significant impact in a leading company.
As the International Product Compliance Manager, you will be instrumental in building international product compliance administrative programs, managing product testing, and supporting product standard and industry initiatives.
Join us as we transform the compliance capabilities of our building products division!
About the Role:
In this high-level compliance support role, you will focus on ensuring our building products meet the necessary compliance standards in European markets.
By leveraging resources, tools, and a commitment to excellence, you will create value and drive compliance efforts that keep Georgia-Pacific at the forefront of the industry.
Your unique contributions will be key to our success.
This is a remote role with travel to European markets.
Responsibilities:
* Provide expert compliance support, focusing primarily on European market requirements.
* Assess building codes and certification program applicability to our products.
* Determine country-specific requirements and ensure they align with our products.
* Seek, obtain, and maintain necessary certifications.
* Develop and maintain ongoing compliance programs.
* Design and implement test plans for building products in the European market.
* Engage with trade and test standard organizations that influence the European market.
* Collaborate with the broader compliance team to leverage learnings from the North American market
(Basic Qualifications):
* Understanding of building and technical standards relevant to the European market.
* Proficiency in Microsoft Office Suite (Teams, Word, PowerPoint, Outlook, Excel).
* Ability to travel approximately 20% to Europe and North America.
What Will Put You Ahead:
* Knowledge of European test standards and certifications, as well as Oceania (AUS/NZ) standards.
* Experience in fire or roof assembly testing.
* Proficiency in English and Spanish, French, or German.
* Familiarity with gypsum products
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...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-06-20 08:38:37
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Sevilla, Spain
Job Description:
MSL IMMUNOLOGY – GASTROENTEROLOGY (SUR - TEMPORAL)
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
About Immunology
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 Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases.
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
MEDICAL SCIENTIFIC LIASON, SOUTH
The role is a field-based role available in multiple cities accross the South region of Spain, including regional travelling (involves extensive Leading Specialists interactions).
We are searching for the best talent for MEDICAL SCIENTIFIC LIASON in SOUTH SPAIN
Purpose: To maximize company product value through high scientific quality communication with Leading Specialists on a peer-to-peer basis.
Accordingly, to strategic lines of Medical Affairs Plan, the MSL is jointly responsible for achieving short-term and long-term company goals at local level.
To be a therapeutic area scientific expert, responsible for discussing our products, patients’ treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) and to be considered an internal and external trusted scientific counterpart.
You will be responsible for:
MSLs should have their own Activity Plan and personal ...
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Type: Permanent Location: Sevilla, ES-SE
Salary / Rate: Not Specified
Posted: 2025-06-20 08:28:29
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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:
Capital Sales -- MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Albany, New York, United States of America, Buffalo, New York, United States, Cincinnati, Ohio, United States of America, Cleveland, Ohio, United States, Columbus, Ohio, United States, Fort Wayne, Indiana, United States, Indianapolis, Indiana, United States, Rochester, New York, United States, Syracuse, New York, United States, Warsaw, Indiana, United States of America
Job Description:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for a Capital Equipment Sales Manager – Spine for the Ohio, Indiana and Upstate New York region.
Ideal candidate will reside in this region with access to a major airport due to travel needs of the role.
Purpose:
Reporting to the Spine Enabling Technologies Leader, the Capital Equipment Sales Manager will serve as the point person for end-to-end commercialization. This will include sales and capital program management for all DePuy Synthes capital platforms in Spine, including technologies accessed through internal and external, current and future partnerships.
The Capital Equipment Sales Manager will be primarily responsible for developing and executing business plans for assigned territories, strategizing and delivering technology demonstrations, presenting customers with various capital equipment acquisition options, and driving the capital sales process to completion.
This position will coordinate efforts with local implant clinical selling teams and Strategic Customer Group account leaders to ensure the customer achieves the desired performance goals for implant performance-based programs.
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-06-20 08:28:13
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Jacksonville, Florida, United States of America
Job Description:
We are searching for the best talent to join our Vision team as a Clinical Operations Manager located in Jacksonville, FL.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Purpose:
The Clinical Operations Manager develops strategies to address complex clinical issues.
He/she manages the strategic elements of study conduct, ensuring that operating procedures and company policies are followed.
Develops and manages timelines, resourcing and budget for all JJV clinical trials.
As spokesperson and technical expert for clinical operations, provides compelling rationale for decisions and presents complex strategies in a clear message.
Using the Clinical Operations Manager’s conceptual knowledge of all R&D functions, drives innovation within functional area.
Establishes key operating practices for department/project while ensuring cross-functional synergy.
Builds cross-functional and cross-departmental support for innovative solutions and mentors/facilitates successful team behavior.
Partners with Platform Managers and Research Optometrists/Ophthalmologist/Clinicians to ensure that project deliverables are met.
Manages relationships externally with Strategic Partners, including universities, research institutions, and CROs.
You will be responsible for:
* Own processes and information required to execute and support the clinical trial including clinical trial project plan, project timelines, resourcing, budget plans, and statements of work
* Accountable for the preparation and fin...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2025-06-20 08:28:06
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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:
R&D Product Development
Job Sub Function:
Biomedical Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
We are searching for the best talent for a Staff R&D Engineer, Life Cycle Management located in Raritan, NJ.
Purpose: The R&D Staff Engineer will lead the R&D work-stream on life cycle management (LCM)/base-business projects, representing Ethicon Biosurgery R&D on a portfolio of design and process change projects in the field of Hemostats, Sealants and Adhesion Prevention. This individual will work with other R&D scientists, engineers and cross functional partners in creating files to support existing product improvement, and other life cycle management activities, own Design History Files for LCM project Design and Process Changes, own Design Requirements Matrices for LCM project Design and Process Changes to ensure quality and regulatory compliance.
Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position will:
* Lead the R&D work-stream on life cycle management (LCM)/base-business projects, representing Ethicon Biosurgery R&D on a portfolio of design and process change projects in the field of Hemostats and Sealants
* Own Design History Files for LCM project Design and Process Changes
* Own Design Requirements Matrices for LCM project Design and Process Changes
* Lead testing on competitive products, and develop strategies on competitive testing, prepare technical reports for use in marketing assets by commercial teams
* Lead activities for complaint handling for marketed products
* Participate in cross-functional project teams in a technical leadership role to drive the development of product requirements, concept generation, process identification, process scale-up and design control for hemostasis, tissue sealant, and adhesion prevention products
* Contribute inventions, new designs, or techniques to solve technical problems or improve existing products or processes.
* Work with in-house teams, cross J&J teams, and external collaborators including companies, universities and consultants to align project strategies with the regulatory, preclinical, and clinical strategies for innovative products to meet business objectives.
* Responsi...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-20 08:28:05
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science Portfolio Management
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
We are searching for the best talent for Associate Director, Global Data, Platforms & Partnerships - GCSO to be in Raritan, NJ.
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Purpose:
The Associate Director, Global Data, Platforms & Partnerships is a hands-on, hybrid role of data steward & data feasibility analyst.
The Associate Director will have data stewardship responsibilities that include governance and support for several datasets, to ensure data quality, integrity, security and compliance.
He / She will partner with the technology team to maintain and update metadata repositories, ensuring that data definitions, data dictionaries, lineage, and relationships are well documented and accessible to users.
He / She will develop deep familiarity with the various real-world datasets such as Optum, IBM Merative MarketScan, Flatiron, etc, that exist within the global data lake.
The Associate Director will partner with data users across the company, to understand data requirements, evaluate real world data sources, and conduct analyses to determine the feasibility of the various data sets and recommend the best data source to answer a key business question or a key research question.
You will be responsible for:
Major responsibilities of this role are data stewardship, data intelligence and data feasibility.
This position entails a significant amount of hands-on analytics responsibility.
Key partnership will be with the internal global commercial data science and real-world evidence teams for key commercial and research activities.
In addition, there will be close partnership with J&J Technology (JJT) data sciences.
This position will report to the Senior Director, Global Data, Platforms & Partnerships.
This includes the following:
Data Feasibility
* Collaboration: Work with data users across the company to underst...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-20 08:28:01
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Albany, New York, United States of America, Athens, Georgia, United States of America, Cincinnati, Ohio, United States of America, Dallas, Texas, United States, Irvine, California, United States of America, Jacksonville, Florida, United States of America, Las Vegas, Nevada, United States, Memphis, Tennessee, United States of America, Piscataway, New Jersey, United States of America, Raynham, Massachusetts, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Experienced Data Engineer! This role can be performed remotely anywhere within the United States.
Remote work may be considered on a case by case basis and if approved by the business.
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/.
Position Summary:
As a Data Engineering for J&J MedTech Quality, you will play a pivotal role in building the modern cloud data platform by demonstrating your in-depth technical expertise and interpersonal skills.
In this role, you will be required to focus on accelerating data products development as part of the fast-paced data platform team.
We are a diverse and growing team, that nurture creativity, deep understanding of data processing techniques, and the use of sophisticated analytics technologies to deliver results.
Data Engineering Responsibilities (70%)
* Develop, optimize, and maintain complex SQL queries, and scripts for data transformation, validation, and reporting!.
* Build and handle data pipelines in Azure, maximising services such as Azure Data Factory, Azure Synapse Analytics, and Databricks.
* Design and implement ETL/ELT processes to integrate data from different sources into a centralized data lake or warehouse!.
* Ensure data integrity, security, and compliance with regulatory standards such as GxP and data governance policie...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-06-20 08:27:53
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Primary Care Physicians (Commission)
Job Category:
Professional
All Job Posting Locations:
Montréal, Quebec, Canada
Job Description:
Spécialiste des comptes cliniques
Johnson & Johnson MedTech Électrophysiologie est présentement à la recherche d’un ou d’une spécialiste des comptes cliniques à Montréal et les environs.
Il s'agit d'un poste permanent à temps plein.
Johnson & Johnson Medtech (JJMT), une division de Johnson & Johnson Inc., commercialise et distribue des solutions d'appareils médicaux destinés à être utilisés dans des établissements de soins de santé primaires et institutionnels partout au Canada.
JJMT se concentre sur la fourniture d'options de traitement minimalement invasives couvrant diverses procédures médicales et états pathologiques.
Parmi les produits représentés par ses différentes unités commerciales, citons : les instruments chirurgicaux, les implants orthopédiques, les dispositifs pour la santé des femmes, y compris les soins du sein, la prévention des infections et les stérilisateurs à usage général, les solutions pour hernies, les produits hémostatiques, les diagnostics et les traitements cardiovasculaires et neurovasculaires.
Biosense Webster Inc.
(BWI), membre de la famille d'entreprises de Johnson & Johnson Medtech , allie un esprit d'entreprise, une technologie de pointe et l'impact mondial de Johnson & Johnson.
Will Webster a mis au point le premier cathéter cardiaque pratique à pointe dirigeable il y a une trentaine d'années et s'est ensuite associé aux innovations de pointe de Biosense Webster International (BW) dans le domaine de la visualisation des signaux intracardiaques.
Aujourd'hui, BW est reconnu dans le monde entier comme un leader de l'industrie dans le développement de solutions innovantes pour les arythmies cardiaques.
Guidés par les besoins des électrophysiologistes et de leurs patients, nous avons été à l'origine d'avancées technologiques allant du premier cathéter dirigeable au cathéter de cartographie avec technologie TRUErefTM OptrellTM , en passant par le système de cartographie et de navigation cardiaque tridimensionnelle le plus sophistiqué d'aujourd'hui (système de cartographie CARTO 3), avec une technologie de cathéter d'ablation par force de contact intégrée.
Une vaste expérience, une attention constante et une technologie de pointe c...
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Type: Permanent Location: Montréal, CA-QC
Salary / Rate: Not Specified
Posted: 2025-06-20 08:27:39
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
People Leader
All Job Posting Locations:
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; Cultivate an environment that...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-06-20 08:27:31
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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: 2025-06-20 08:27:26
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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:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
People Leader
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
Basic purpose of the role
* Leading the EH&S organization for Janssen Biologics (JBV) site in the Netherlands (NL).
This consists in deploying, leading, and implementing EH&S strategies, policies, plans, procedures for JBV.
Key outcome is ensuring the EH&S team has taken all needed EH&S precautions to assure continuous, EH&S reliable & compliant supply chain, research & development activities, and is continuously improving in the field of EHS.
* Familiar with the annual company /division goals and aware of how he/she can influence these through his/her performance.
* Results achieved through effective leadership of the JBV EH&S team and through effective collaboration / influencing key leadership teams on the JBV EHS team as well as with J&J global EH&S.
All their needs/ improvements to be balanced with global/ local context.
The EH&S lead decides how to convert these in a lean, results oriented, compliant EHS approach.
* Responsible for developing and coordinating site EHS&S infrastructure to help GM & Site Management to ensure compliance with legislative and J&J requirements.
* Partner with Site LT to establish and implement site EHS&S strategy and Management Action Plan (MAP) in alignment with the J&J requirements.
* Responsible for site EHS&S department including budget (OPEX &CAPEX)
* Coach and mentor line management to take ownership of EHS&S.
* Ability is to reach outside J&J and represent the JBV EH&S team when meeting with governmental inspectors for the site.
Key Responsibilities
* Shared responsibility with site General Manager for EHS&S performance at the site.
Responsibility to provide advice to Site Manager for EHS&S performance at the site.
* Partner with local Management to develop and implement a site MAP to address EHS&S program deficiencies and ensure EHS&S regulatory compliance.
* Build effective working relationships with staff and key stakeholders including corporate EHS&S function and regulatory authorities.
* Develop EHS&S objectives for the site - auditing, analyzing, documenting, reporting on their implementation / effectiveness to management via dashboards, reports & management re...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-20 08:26:58
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ERM is seeking highly motivated Consultant, Archaeologist to join our global consulting firm as part of our Cultural Resources Services team.
This is a hybrid full-time position based out of our Irvine ERM office.
Applicants are to be familiar with the relevant California and regional regulatory processes (i.e., federal, state, and municipal).
California archaeological field experience is highly desired.
Successful candidates must be flexible and responsive to a challenging and changing work environment where schedules and tasks fluctuate according to the needs of the projects and clients.
The successful candidate will also provide technical assistance for archaeological desk and field studies for clients within the United States.
RESPONSIBILITIES:
* Conduct research and writing for cultural resource heritage components of state laws, NHPA Section 106, and NEPA documents for projects for private and government sector clients.
* Perform literature review, field reconnaissance, field surveys, and excavation for archaeological studies.
* Access online cultural resource databases.
* Perform research and write technical reports.
* Provide technical consulting skills to support the growth of ERM’s business and client base in the area of archaeology and cultural heritage.
* Interact with other ERM practice areas to share multi-disciplinary resources and best practices across the country.
REQUIREMENTS:
* Bachelor’s degree in Anthropology, Archaeology, or closely related field of study.
Or equivalent experience.
* 2+ years of related professional experience of west coast regional cultural areas.
* Located in Southern California and willing to perform field work.
* Ability and willingness to frequently travel to field sites that will be located in and out of state.
* Must be able to walk long distances (up to ten miles per day) in varying terrain under adverse conditions, including inclement weather, wildlife encounters, and able to lift and carry up to 50 lbs., and able to excavate shovel tests.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* Previous experience with mapping equipment and other special application equipment (e.g., total station, GPS, tablets etc.).
* Demonstrated experience completing inventory, survey, testing, and/or data recovery.
* Familiarity with online databases, including AGOL.
* Experience as contributor to technical reports.
* Must have strong attention to detail in documentation of work.
* Strong oral and written communication and computer skills.
* Ability to work within a team as well as independently.
* Strong proficiency in Microsoft Office Suite.
PREFERRED QUALIFICATIONS:
* Ability to be listed on BLM cul...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-20 08:24:52
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Your Job
Georgia-Pacific, LLC (GP) is now hiring a R&D Process Engineer for its Tolleson, Arizona Mailers facility.
The R&D Process Engineer supports manufacturing on site including equipment installation, training, acceptance testing, performance testing, and process and equipment upgrades.
The R&D Process Engineer must be able to present data in a concise way to both technical and non-technical audiences.
We believe in the challenge process and this person must be open to the ideas and recommendations of others to create the best outcome for both the site, R&D and i2.
Typical work schedule would be weekdays from 8am-5pm.
Our Team
The GP Tolleson facility employs about 115 people and serves converting customers throughout the Southwest with sustainable packaging products.
This position provides opportunities for promotion within GP Tolleson, as well as many other Georgia-Pacific and Koch facilities across the country.
Come join our team!
You know us already! Georgia-Pacific is one of the nation's leading corrugated sheet and box manufacturers.
Check out these videos/links to learn more about the Corrugated Business at Georgia-Pacific:
www.gppackaging.com
What You Will Do
* Actively engage with Operations, Maintenance, and R&D to identify opportunities for evolutionary changes to the process and equipment
* Update process control and troubleshooting procedures and train plant personnel on current and updated process procedures
* Identify and lead process improvement projects to improve OEE (Overall Equipment Effectiveness)
* Translate learnings and technology upgrades from other sites and work with EHS and site operations to deploy on site
* Support new customer and product trials and production campaigns
* Employ process control best practices and strategies to centerline the process
Who You Are (Basic Qualifications)
* Bachelor's degree in engineering or science
* Previous experience using Microsoft Office programs and other software programs to present data (Word, Excel, Outlook, Teams, Power Bi, etc.)
* Previous experience in a manufacturing facility
* Previous experience moderating meetings and training sessions
* Must be willing and able to travel up to 25%
* 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 in Mechanical, Chemical or Electrical Engineering
* 2+ years of hands-on experience in a manufacturing facility interfacing with quality, operations leadership, maintenance and hourly employees
* Previous experience within a corrugated and/or converting manufacturing facility
* Previous experience developing and executing experiments and monitoring process data
* Previous experience leading process improvement initiatives
* Previous experience in data analysis and/or statistical software (JM...
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Type: Permanent Location: TOLLESON, US-AZ
Salary / Rate: Not Specified
Posted: 2025-06-19 09:09:28
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Classification:
Non-Exempt
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The Soil Counter/Sorter handles, counts, sorts and records incoming soiled textiles from the customer.
Identifies damaged or abused textiles.
Prepares and transfers textiles to other departments.
Performs other tasks as needed.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Open bag of soiled textiles, then sort them by type, size and color.
- Count textiles manually or electronically, and transfer them into sorting systems.
- Identify damaged or abused textiles and record into sorting systems.
- Meet efficiency and safety standards for the position.
- Follow instructions as directed by supervision.
Additional Functions:
- Work in other production positions as needed.
Qualifications:
- Recognize colors and sizes, count accurately.
- Comprehend and follow direction.
Typical Physical Activity:
- Physical Demands consist of standing, walking, reaching overhead, pushing, pulling, grasping, lifting up to 50 lbs.
and stooping.
- Physical Requirements consist of being able to meet the physical demands for the entire shift.
Typical Environmental Conditions:
- Production areas of a typical industrial laundry facility, which includes variations in temperature, odors, humidity, lint and dust.
Soiled linens come from a variety of customers such as restaurants, hotels, medical facilities and shops.
Travel Requirements:
- none.
Education:
- none.
For a general description of benefits that are being offered for this position, please visit alsco.com/benefits.
Alsco is an Affirmative Action/Equal Employment Opportunity Employer.
Revised: 04/29/2022
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment...
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Type: Permanent Location: Reno, US-NV
Salary / Rate: Not Specified
Posted: 2025-06-19 09:08:37
