Salario: Program Mánager en España

Joining Ecolab as part of our new Supply Chain Graduate Scheme is a great opportunity to join a company that makes a difference.We make the world a cleaner, safer and healthier place.Our products and technologies prevent disease and infection, keep food supplies safe and protect the places where people eat, sleep, work, play and heal.Ecolab has recently been named to Forbes’ list of Best Employers for New Grads! So, not only do you get to work in a team that will give you the opportunity to work with people from all cultures and backgrounds to deliver a single goal, you will also get to work for one of the best employers around! What to expect? We're offering the opportunity to join our rotation program.From day one you will be exposed to making a difference in real life situations, projects and jobs.We'll give you an experience of working across the whole range of disciplines within our Supply Chain, including manufacturing, logistics, planning, lean and engineering.Our Supply Chain helps keep us meeting our customer expectations, with over customer locations and a turnover of $15bn per year, this is no small task.We will support you as you embark on your journey with Ecolab whilst giving you space to grow and learn at your own pace.What you’ll need? We are interested in meeting individuals with diverse backgrounds.Engineering (Industrial, Chemical, Mechanical), Chemistry, Health, Safety & Environment and Business Degrees & Supply Chain at an Undergraduate or Master’s level.Desire to grow and develop your expertise across a wide range of disciplines within a cross-border supply chain team Fluency in English and Spanish Knowledge of another European language beneficial Being self-driven and motivated to grow and develop Proven ability to adapt to new challenges and excel in an every changing environment Demonstrated problem solving skills and creative thinking Excellent communication and presentation skills and cultural sensitivity Experience working with.Microsoft Excel, PowerBI, PowerApps and other data visualization/automation tools Located in the Barcelona area with flexibility to relocate to Celrá (1 year of rotation will be in Girona) What you’ll get? Working at Ecolab is more rewarding than just helping to make a difference in the world.It's about being part of a team that gets results, has fun and makes huge positive contributions to the lives of others.What's more you'll be rewarded with an exciting chance to grow and develop your career in a world leading organisation.We offer a competitive salary and attractive benefits package and the chance to be part of a world leading Supply Chain.The Supply Chain Graduate Scheme begins in September .Who are we? At Ecolab we find solutions for the world's biggest problems.Around the globe, our customers trust us to keep their environments clean and safe, help them to operate efficiently and to achieve their sustainability goals.Partnering to help solve global challenges is what we do best, and our new roles in the Supply Chain Program are critical to this success.You are empowered to make an impact right away.Success in this team is about cooperating and partnering effectively with others and working ethically to deliver results.Working in the team gives an opportunity to work with people from all cultures and backgrounds to deliver a single goal.Own your future.Impact what matters.#li-eu Ecolab (NYSE.CL), socio confiable alrededor de tres millones de clientes en diferentes partes del mundo, es líder mundial en sustentabilidad y ofrece soluciones y servicios de agua, higiene y prevención de infecciones, que protegen a las personas y los recursos vitales.Con un siglo de historia e innovación, Ecolab cuenta con ventas anuales de $14 mil millones y más de asociados.Ecolab ofrece soluciones integrales basadas en evidencia científica, información basada en datos y un servicio de primer nivel para avanzar en la seguridad alimentaria, mantener los entornos limpios y seguros y optimizar el uso del agua y la energía.Además de mejorar la eficiencia operativa y la sustentabilidad para los clientes en los mercados de alimentación, atención médica, ciencias biológicas, alojamiento e industria en más de 170 países en el mundo.Cuando comience a trabajar en Ecolab, se enfrentará con algunos de los desafíos más significativos del mundo y tendrá la oportunidad de aprender y crecer, dar forma a su carrera, crear impacto y ver rápidamente la importancia de su trabajo.Para obtener más información y novedades de Ecolab, visite www.colab.om.

Formación en.Ciencias Ambientales, Biología, Ingeniería (Ambiental, Industrial, Forestal, Química) o titulación similar -Conocimiento profundo y experiencia sustancial en la aplicación de estándares críticos de contabilidad, informes y establecimiento de objetivos, especialmente GHG Protocol, SBTi, TCFD, y CDP -Idiomas.Castellano (C1), Inglés (C1) -Informática.Nivel avanzado en el uso de herramientas de modelado y manipulación de datos -Gestión de proyectos de gestión de carbono, ya sea en la empresa o en un entorno de consultoría -Gestión de equipos de trabajo -Trato con clientes y relaciones comerciales Ocupación.TÉCNICOS EN MEDIO AMBIENTE Requisitos Conocimientos Formación reglada - Certificados de profesionalidad Se debe estar en posesión de alguno de los siguientes títulos o certificados.LICENCIATURA en Ciencias Ambientales GRADO en Ciencias Ambientales LICENCIATURA en biología

Empresa sector Cárnico |AragónImportante empresa del sector cárnico en Aragón.Reportando al Responsable Comercial, la persona seleccionada se encargará de:Prospectar clientes en la zona asignada (Asia y México).Conservar y recuperar clientes. Soporte continuo a los clientes. Gestión de pedidos.Resolución de incidencias. Elaboración de estrategia junto con el equipo comercial. Oportunidades de carrera en el sector cárnico.Proyecto estable.

At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world’s the most significant healthcare challenges.Our Corporate, Consumer Health, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives.With a reach of more than a billion people every day, there’s no limit to the impact you can make here.Are you ready to re-imagine healthcare?   Here, your career breakthroughs will change the future of health, in all the best ways.And you’ll change, too.You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love.Amplify your impact.Join us!   Johnson & Johnson is recruiting for a Summer Intern, located in Jacksonville, FL (hybrid).  Regulatory Affairs Opportunities.  Regulatory affairs is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, medical devices and consumer products among others, and by the companies responsible for the discovery, testing, manufacture and marketing of these products wanting to ensure that they supply products that are safe and make a worthwhile contribution to public health and welfare.  Key Responsibilities.  Experiences Include.  Assist in the compilation of requirements for global regulatory submissions of our products.  Support the acquisition and management of files to meet applicable regulations   Attend project team meetings with RA lead to assist in strategic discussions to hone team collaboration skillset   Learn regulatory affairs competencies to ensure product registration lifecycle processes compliance   Evaluate current processes and propose opportunities for efficiencies/improvements   Data analytics from regulatory information management systems (RIM) and reports / dashboards /presentations development.  US and Global Regulatory Policies Understanding and Shaping activities.  Qualifications Education.  Currently enrolled full-time and have completed at least 2 years in an undergraduate program, or enrolled full-time in a graduate program (M.., M.., Ph..or M..), pursuing a degree majoring in a scientific, technology, engineering, business or law related field.Examples include, biomedical, biochemical, civil, mechanical, or electrical engineering, data analytics/applied statistics, quantitative modeling in biology, pharmacy, pharmaceutical sciences, life sciences, medical / scientific writing or public health administration.  Candidate must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.., H1-B status) now or in the future.  Experience and Skills.  Required.  Available to work full-time (40 hours per week) during Summer .  Candidates need to be proficient with Microsoft Office, Word, Excel (including a high proficiency with generating pivot tables and graphs), and Power Point, and have strong oral and written communication skills.  Additional technical competencies in SharePoint, Teams and other information technology systems are highly desirable.  Able to work individually, as well as, part of a group, with curiosity and flexibility.  Possess a “can do” approach, and courage to speak your voice and suggest innovative ideas.  Assignment location will be hybrid on-site in Jacksonville, Fl.  Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. 

Join our global team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.Job Description SummaryJob DescriptionTHE DIRECTOR ROLE, REGULATORY AFFAIRSThe Director, Regulatory Affairs Medtech is a critical member of the Alira Health project team. The Director will work closely with Managers and VP and work with clients to guide, write and streamline regulatory projects. The Director will help to set direction for clients in the coordination, execution, guidance and implementation of regulatory programs, requirements and compliance activities. The individual will be a key resource for all regulatory activities.The main focus of the Director will be to work on EU and FDA-related projects. Expertise in both markets is not a must, but it is preferred if the Director is willing to continue learning in case of lower expertise in one of both markets before mentioned.ESSENTIAL JOB FUNCTIONSBe hands-on on planning, organizing, executing, writing and delivering projects.Monitor and analyze the impact of emerging or revised laws, regulations, enforcement actions and other changes that impact the manner by which the clients' products are regulated around the world.Plan, manage, prepare and submit EU/NB-related submissions: Roadmaps, Gap Analysis, Product categorization, Technical Documentation compilation, Response to non-conformities, etc.Plan, manage, prepare and submit FDA-related submissions: RFD, Pre-Submissions, 510(k), De Novo, PMA, IDE, BDD, etc.Provide, as needed, regulatory strategic support and direction to client programs and initiatives.Design and implement regulatory strategies to obtain, maintain and extend product registrations for new device/combination product/companion diagnostic portfolios.Oversee the development and submission of regulatory filings to FDA and EUServe as liaison with regulatory agencies.Lead core regulatory activities to ensure effective agency interactions that are consistent with clients regulatory strategies.Provide regulatory guidance and input to clients.Provide regulatory operations and electronic submissions support.Performs additional duties as assigned.PREPARATION, KNOWLEDGE, SKILLS ABILITIESBS/BA from a top undergraduate program in a scientific discipline.10+ years experience in a regulatory role within medical device sector.Knowledge of appropriate regulations within the specific sector.Previous experience in consulting will be favorably valued.Knowledge of FDA procedures.Knowledge of MDR and IVDR.Strong analytical skills and ability to problem-solve unstructured or ambiguous challenges.Demonstrated ability to communicate complex information and analyses to a variety of audiences.The role for Director requires ability to work hands-on on the execution and delivery of the projects.Strong command of English, both written and verbal.Excellent communication and interpersonal skills with client service orientation.Advanced skills in MS Office Suite, particularly Word.Thrives in collaborative, yet less structured team environment.We will not sponsor work visas.WORKING CONDITIONS/PHYSICAL DEMANDSNormal office working conditions including frequent sitting, standing, bending, twisting and computer monitor use.LanguagesEnglishEducationContract TypeRegularSummaryLocation: Barcelona; Barcelona-RemoteType: Full time