Ofertas de empleo de Jefe/a de Proyectos en València

• Flexibilidad horariaSí
• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada13 abr.

Teletrabajo . Javascript PHP Python ERP Office

About usLegit.Health deploys computer vision and artificial intelligence technology to enable lifesaving diagnosis and therapies for visible diseases.

Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone everywhere.

Things you should know before following and signing up for the position:

We are a startup, it is important that you are knowledgeable about how startups operate and know that at this stage there are more unknowns than certainties.

There are many things to discover and define yet, so you will be part of that definition, therefore you will have many functions helping the management.

At Legit.Health we have a friendly open collaborative culture and a united team vision.

We love entrepreneurial/risk taking/high ambition mindsets.

Our work is rewarding and we help each other win by creating a supportive and collaborative environment for one another.

Take a look at our opening below and send us your application - we look forward to hearing from you!

Job description We are on the lookout for a passionateLife Science Project Managerwith a focus onclinical trialsand healthcare innovationand a specialization insoftware medical devices, eager to drive innovation in the evolving landscape of digital health.

This pivotal role involvesleading the development and implementation of transformative projectsin healthcare technologyfrom conception to delivery.

The ideal candidate willbridge the gap between commercial, clinical and technical teams,translating customer needs into actionable specifications, and ensuring our solutions not only meet the high standards required by our health sector partners and their patients but also stay within budget and time constraints while adhering to regulatory requirements.

A key part of your role will beworking with partners (hospitals, CROs, and research institutions), ensuring proper study design, execution, and integration of our technology into customer workflows.

Note On Collaboration And Roles

You'll work alongside aDeal Owner, who leads thecommercial relationship, and aCustomer Success Manager, responsible for post-sale client engagement and support.

This setup allows you to focus onimplementation, delivery, execution, and providing clinical, technical and regulatory advisory to the customer—without managing the client relationship end-to-end.

Your responsibilities will center ontranslating clinical and business needs into clear project plans and specifications, ensuring successful execution across all phases.

While deep technical expertise is not required, asolid foundational understanding of data and technical concepts—such as database structures, data transfer specifications, integrations, and system requirements—is essential to effectively coordinate with technical teams and support seamless projects from definition to the delivery.

You will also provide clinical, technical, and regulatory guidance to customers —without being responsible for managing the full client relationship lifecycle.

What you need to achieveProject planning and execution:Develop and track detailed project plans, manage changes to project scope, schedule, ensuring successful project execution within time, and scope constraints.

Daily customer interaction:Collaborate with customers, investigators, CROs, and Sponsors to ensure project success

Team liaison:Act as the crucial link between the commercial team and the product team, facilitating effective communication and ensuring customer needs translate into clear and achievable technical specifications.

Technical and regulatory customer advisory:Provide expert support to help customers generate and understand the best use case for our software medical device, including explaining technical aspects related to product, as well as regulatory feasibility and data protection issues.

Functional and Technical requirements analysis:Thoroughly assess project needs and specifications to ensure alignment with product objectives and customer expectations.

Holistic view of healthcare processes:Offer a comprehensive perspective of healthcare processes to help and support the team in developing effective solutions.

Development specifications and Product documentation Definition:Clearly establish development requirements and ensure the creation of accurate and complete product documentation.

Product strategy participation:Actively contribute to the definition and adjustment of product strategy, ensuring its relevance and success in the market.

Must haveStrong knowledge ofGood Clinical Practice (GCP)and clinical research regulations

Proven experience in project management, especially in the development of software medical devices within the health, biotechnology, or digital health sectors (hospitals, CROs, Sponsors, research institutions).

Specific knowledge of AI technologies applied to health and previous experience in dermatology or related fields.

Understanding of medical device regulation, including familiarity with software medical device regulatory frameworks and compliance.

Basic knowledge of data protection laws, such as GDPR and HIPAA compliance, to ensure our products meet the necessary data privacy and security standards.

Deep understanding of the health industry, including B2B dynamics and specific regulations for software medical devices.

Exceptional communication skills, capable of effectively interacting with technical teams, healthcare professionals, and business stakeholders, explaining complex concepts in a clear and accessible manner.

Effective leadership, with experience leading multifunctional teams in dynamic and demanding environments.

Degree in Business Administration, Health Management, Biotechnology or a related field.

Project management certification (e.g., PMP, PRINCE2) is highly valued.

Nice to haveExperience withdata transfer specifications, database structures, and system integrationsin the context of clinical or research studies.

Familiarity withclinical data management systems (CDMS), electronic data capture (EDC) platforms, and clinical trial software (e.g., Medidata, REDCap, OpenClinica).

Knowledge of healthcare processes and management systems, such as HIS/EHR/EMR, RIS, LIS, PACS, or ERP, as well as standards like FHIR and HL7v2.

Foundational programming knowledge in programming languages such as PHP, JavaScript, or Python.

ImportantAble to work autonomously, with discipline and with high motivation and energy

Proactive, willing to learn, have an impact and grow in the company

Team player capable of adapting to changes in a fast-paced environment

What do we offer ?Full-remote position.

We are a team of committed professionals, so you choose where you work from and also means that all processes need to be thought of as if we had no office and everyone is working remotely.

No one will feel like an outsider, since all conversation will need to happen on slack or hangouts.

Working in a fast growing Start-up environment within an international context

Flexible compensation: daycare and restaurant

Flexible vacation policy: 23 working days per year + 2 additional days granted by the company (your birthday and December 7th) + 2 days for company closure per labor agreement (December 24th and 31st)

Flexible working hours

Full time contract

Starting day: as soon as possible.

Competitive salary according to your experience

LanguagesHigh Spanish and English proficiency (writing and speaking).

Additional languages are a plus

In compliance with the provisions of the data protection regulations, we inform you that the personal data you have provided with your resume will be processed in a mixed manner (automated or not) by AI Labs Group, S.L., with NIF B******** and address in Gran Vía, 1, BAT Tower, Bilbao (Bizkaia), ***** (hereinafter, Legit.Health).

The purpose of this data processing is the management of Legit.Health's personnel selection processes and is based on your prior consent.

Your data will be kept for one year, after which we will proceed to cancel it.

You are also informed that no automated decisions will be made.

Your data will not be transferred to third parties.

At any time you can exercise your rights of access, rectification, deletion, portability, limitation, or opposition, by writing to the email ******.

We also inform you that you can go to the Control Authority to assert your data protection rights.

• Please note that this is not an email to submit job applications.
  
  

• Flexibilidad horariaSí
• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada13 abr.

Teletrabajo . Javascript PHP Python ERP Office

About us Legit.Health deploys computer vision and artificial intelligence technology to enable lifesaving diagnosis and therapies for visible diseases.

Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone everywhere.

Things you should know before following and signing up for the position: We are a startup, it is important that you are knowledgeable about how startups operate and know that at this stage there are more unknowns than certainties.

There are many things to discover and define yet, so you will be part of that definition, therefore you will have many functions helping the management.

At Legit.Health we have a friendly open collaborative culture and a united team vision.

We love entrepreneurial/risk taking/high ambition mindsets.

Our work is rewarding and we help each other win by creating a supportive and collaborative environment for one another.

Take a look at our opening below and send us your application - we look forward to hearing from you!

Job description We are on the lookout for a passionate Life Science Project Manager with a focus on clinical trials and healthcare innovation and a specialization in software medical devices , eager to drive innovation in the evolving landscape of digital health.

This pivotal role involves leading the development and implementation of transformative projects in healthcare technology from conception to delivery .

The ideal candidate will bridge the gap between commercial, clinical and technical teams , translating customer needs into actionable specifications , and ensuring our solutions not only meet the high standards required by our health sector partners and their patients but also stay within budget and time constraints while adhering to regulatory requirements.

A key part of your role will be working with partners (hospitals, CROs, and research institutions), ensuring proper study design, execution, and integration of our technology into customer workflows .

Note on collaboration and roles: You'll work alongside a Deal Owner , who leads the commercial relationship , and a Customer Success Manager , responsible for post-sale client engagement and support.

This setup allows you to focus on implementation, delivery, execution, and providing clinical, technical and regulatory advisory to the customer — without managing the client relationship end-to-end.

Your responsibilities will center on translating clinical and business needs into clear project plans and specifications , ensuring successful execution across all phases.

While deep technical expertise is not required, a solid foundational understanding of data and technical concepts —such as database structures, data transfer specifications, integrations, and system requirements—is essential to effectively coordinate with technical teams and support seamless projects from definition to the delivery.

You will also provide clinical, technical, and regulatory guidance to customers —without being responsible for managing the full client relationship lifecycle.

What you need to achieve Project planning and execution: Develop and track detailed project plans, manage changes to project scope, schedule, ensuring successful project execution within time, and scope constraints.

Daily customer interaction: Collaborate with customers, investigators, CROs, and Sponsors to ensure project success Team liaison: Act as the crucial link between the commercial team and the product team, facilitating effective communication and ensuring customer needs translate into clear and achievable technical specifications.

Technical and regulatory customer advisory: Provide expert support to help customers generate and understand the best use case for our software medical device, including explaining technical aspects related to product, as well as regulatory feasibility and data protection issues.

Functional and Technical requirements analysis: Thoroughly assess project needs and specifications to ensure alignment with product objectives and customer expectations.

Holistic view of healthcare processes: Offer a comprehensive perspective of healthcare processes to help and support the team in developing effective solutions.

Development specifications and Product documentation Definition: Clearly establish development requirements and ensure the creation of accurate and complete product documentation.

Product strategy participation: Actively contribute to the definition and adjustment of product strategy, ensuring its relevance and success in the market.

Must have Strong knowledge of Good Clinical Practice (GCP) and clinical research regulations Proven experience in project management, especially in the development of software medical devices within the health, biotechnology, or digital health sectors ( hospitals, CROs, Sponsors, research institutions) .

Specific knowledge of AI technologies applied to health and previous experience in dermatology or related fields.

Understanding of medical device regulation, including familiarity with software medical device regulatory frameworks and compliance.

Basic knowledge of data protection laws, such as GDPR and HIPAA compliance, to ensure our products meet the necessary data privacy and security standards.

Deep understanding of the health industry, including B2B dynamics and specific regulations for software medical devices.

Exceptional communication skills, capable of effectively interacting with technical teams, healthcare professionals, and business stakeholders, explaining complex concepts in a clear and accessible manner.

Effective leadership, with experience leading multifunctional teams in dynamic and demanding environments.

Degree in Business Administration, Health Management, Biotechnology or a related field.

Project management certification (e.g., PMP, PRINCE2) is highly valued.

Nice to have Experience with data transfer specifications, database structures, and system integrations in the context of clinical or research studies.

Familiarity with clinical data management systems (CDMS) , electronic data capture (EDC) platforms, and clinical trial software (e.g., Medidata, REDCap, OpenClinica).

Knowledge of healthcare processes and management systems, such as HIS/EHR/EMR, RIS, LIS, PACS, or ERP, as well as standards like FHIR and HL7v2.

Foundational programming knowledge in programming languages such as PHP, JavaScript, or Python.

Important Able to work autonomously, with discipline and with high motivation and energy Proactive, willing to learn, have an impact and grow in the company Team player capable of adapting to changes in a fast-paced environment What do we offer ? Full-remote position.

We are a team of committed professionals, so you choose where you work from and also means that all processes need to be thought of as if we had no office and everyone is working remotely.

No one will feel like an outsider, since all conversation will need to happen on slack or hangouts.

Working in a fast growing Start-up environment within an international context Flexible compensation: daycare and restaurant Flexible vacation policy: 23 working days per year + 2 additional days granted by the company (your birthday and December 7th) + 2 days for company closure per labor agreement (December 24th and 31st) Flexible working hours Full time contract Starting day: as soon as possible.

Competitive salary according to your experience Languages High Spanish and English proficiency (writing and speaking).

Additional languages are a plus In compliance with the provisions of the data protection regulations, we inform you that the personal data you have provided with your resume will be processed in a mixed manner (automated or not) by AI Labs Group, S.L., with NIF B******** and address in Gran Vía, 1, BAT Tower, Bilbao (Bizkaia), ***** (hereinafter, Legit.Health).

The purpose of this data processing is the management of Legit.Health's personnel selection processes and is based on your prior consent.

Your data will be kept for one year, after which we will proceed to cancel it.

You are also informed that no automated decisions will be made.

Your data will not be transferred to third parties.

At any time you can exercise your rights of access, rectification, deletion, portability, limitation, or opposition, by writing to the email ******.

We also inform you that you can go to the Control Authority to assert your data protection rights.

• Please note that this is not an email to submit job applications.
  
  

• Nivel de experiencia---
• Tipo de contratoTemporal
• Publicada10 abr.

. Cloud Coumputing

Company: Celestica Valencia S.A.

Celestica is a Canadian company, world leader in the electronic manufacturing sector. The plant in Valencia focuses its activities in the Aerospace, Industrial and Healthcare areas, producing and assembling high complexity products.

The main differentiator in Valencia facilities are its design capabilities and the various engineering services that it can provide to its customers, creating a differential value beyond the regular electronic manufacturing services.

Area/Department: Design and Engineering Services (D&ES)

The Design and Engineering Services department in Celestica Valencia is specialized in the development of new products and electronic systems for both its customers (mostly international) and the production line within the factory.

The D&ES team is composed by more than 50 specialist engineers: electronics, software, mechanics…that, in the end, build a multiskilled team able to carry on (almost) any kind of development projects.

The areas in which these projects are developed are mainly related with healthcare and in-vitro diagnosis, industrial, aerospace and test development.

Detailed Description

The student will collaborate in different design, administration & project/program management activities related with the on-going projects, always under the guidance and supervision of the responsible engineers and project managers. This will allow the student to acquire and consolidate an extensive set of abilities in electronics product and test system design at various levels.

The student will also participate in the administration of the electronic lab and will collaborate with the management of the group to optimize reporting and management processes. In addition to that, she/he will be involved in activities which will require information exchange with other teams within the organization, but also external parties. This will support her/his soft skills (such as communication or problem solving) development process

She/He will be encouraged to propose new organization, administration or automation ideas in order to optimize existing processes within the group.

She/He will participate as one of the components of the development team, contributing with her/his point of view and proposing solutions and alternatives aimed to overcome the different challenges that a development group presents on a daily basis.

Notes

The work atmosphere is excellent and totally open, a positive attitude constitutes a warranty for the integration in the team, not only at a professional level but also personally.

Personal skills such as teamwork, initiative, accountability and meticulousness on every assigned task will be extremely valued as well as, obviously, the motivation to learn and continuously improve.

Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).

At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

COMPANY OVERVIEW:

Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.

Celestica would like to thank all applicants, however, only qualified applicants will be contacted.

• Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada3 abr.

.

En Liados buscamos a esa persona que sepa leer entre líneas lo que el cliente necesita, que defienda la creatividad frente al presupuesto y sepa gestionar equipos. Si te mueves como pez en el agua entre briefings, timings ajustados y gestión de equipo, queremos conocerte.

¿Qué harás con nosotros?

Gestión De Cuentas

Serás la cara visible ante el cliente, liderando reuniones de seguimiento y detectando nuevas oportunidades de negocio.

Project Management

Planificación de recursos, control de hitos, gestión de entregas y feedbacks.

Interlocución Interna

Coordinación directa con los departamentos de Creatividad, Estrategia y Producción.

¿Qué buscamos en ti?

Experiencia demostrable (mínimo 2-4 años) en agencias de publicidad o productoras.

Capacidad analítica para gestionar presupuestos y KPIs de proyecto.

Excelentes dotes de comunicación.

Dominio de herramientas de gestión.

¿Qué ofrecemos?

Contrato Indefinido

Jornada de 37,5 horas semanales

Oficina en Poblenou

Presencialidad Total

Creemos en la energía del equipo en directo. Trabajarás codo con codo con el equipo en un ambiente de colaboración real.

Explícanos tu experiencia y envíanos tu CV: ******

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada15 ene.

• ¿Quieres trabajar en una ingeniería con grandes proyectos industriales?
• ¿Tienes formación técnica y experiencia como Project Manager?

¿Dónde vas a trabajar?

Nuestro cliente es una ingeniería del sector industrial, con un enfoque en proyectos de construcción innovadores y sostenibles.

Descripción

• Gestionar y coordinar proyectos desde su inicio hasta su finalización en Valencia.
• Gestionar proyectos de estructura metálica, especialmente tanques de almacenamiento.
• Controlar presupuestos, compras y plazos de entrega, asegurando rentabilidad del proyecto.
• Establecer y mantener relaciones con proveedores, contratistas y otros socios clave del sector industrial y de fabricación.
• Elaborar informes de progreso y presentar resultados a las partes interesadas del proyecto.
• Garantizar el cumplimiento de las normativas legales y medioambientales aplicables al sector de la construcción.
• Identificar y gestionar riesgos asociados a los proyectos.
• Optimizar los recursos disponibles para maximizar la eficiencia y la rentabilidad de los proyectos.
• Colaborar con equipos multidisciplinares para garantizar la integración de todos los aspectos técnicos y operativos.

¿A quién buscamos (H/M/D)?

El/la candidato/a seleccionado deberá cumplir los siguientes requisitos:

• Formación universitaria en ingeniería, arquitectura o áreas relacionadas con la construcción.
• Experiencia previa de al menos 4 años como project manager en el sector de la construcción, concretamente haber trabajado estructura metálica.
• Conocimientos sólidos en gestión de proyectos, muy valorable la experiencia en el área de biogás.
• Capacidad para trabajar en equipo y coordinar equipos multidisciplinares. Capacidad de liderazgo.
• Conocimientos en normativas legales y medioambientales aplicables al sector.
• Habilidades para la resolución de problemas y toma de decisiones.
• Comunicar eficazmente en inglés y español, tanto verbalmente como por escrito.
• Disponibilidad para trabajar en Valencia. Y viajar un 30% del tiempo.

¿Cuáles son tus beneficios?

• Contrato indefinido en una empresa consolidada del sector industrial y de fabricación.
• Salario competitivo entre 38.000 EUR y 40.000 EUR brutos anuales. Con plan de carrera.
• Coche de empresa incluido como beneficio adicional.
• Ambiente laboral profesional y orientado a la excelencia.
• Oportunidad de desarrollo profesional en el sector de la construcción y biogás.