375 Ofertas de Qa Qc en España
Qa/Qc Engineer
Hoy
Trabajo visto
Descripción Del Trabajo
At Technip Energies, we believe in a better tomorrow and we believe we can make tomorrow better. With approximately 15,000 talented women and men, we are a global and leading engineering and technology company, with a clear vision to accelerate the energy transition. Designing and delivering added value energy solutions is what we do.
We are currently seeking a QA/QC Engineering Specialist to to join our team based in Madrid.
About the job:
As a QA/QC Engineering Specialist you will set the Quality Control System for the projects and issue the Site Quality Plan in accordance with project Quality Plan and project requirements.
Your main accountabilities will be:
- To be the single point of contact and the accountable person for QA/QC project activities in front of other parties.
- To perform and coordinate all QA/QC activities for the assigned project and/or construction contract.
- To verify the conformity against the contractual requirements during the execution of the Construction, erection and installation activities in terms of execution plan, delivery date and/or manufacturing quality.
- To ensure that all the required information, documentation and QCP's are available at proper time to the Supplier as required by the construction schedule.
- To manage and update the QA/QC MS deliverables in the applicable IT Tools (e.G. EasyPlant, GAIA).
- To analyze the information provided by Construction Contractors and monitors the KPI's evolution.
- To issue QA/QC Project deliverables (Pre‐Inspection Meeting report, Pre‐JSM, PPs, QCPs, CSHs)
- To identify and report any QA/QC deviation or issues impacting deliveries or quality, coordinate the definition of the recovery actions and follow‐up their implementation until their resolution.
- To contribute in the Technical evaluation of offers (related to Construction SOW) and to contribute in the preparation of Construction Contractors and Inspection Agencies performance evaluations.
- To assure the compliance with Local regulations, Project Standards and procedures (in the applicable QC deliverables).
- If required, support to project QC Manager at Site on related QC activities for a limited time.
About you:
We would love to hear from you if your profile meets the following requirements:
- You have a bachelor's degree in industrial, Chemical or Materials Engineering. A master's degree in a Quality-related field will be a plus.
- You have 2-3 years of experience as a QA/QC Specialist.
- Experience in Site working on the setting of the system (elaboration of procedures, elaboration of ITPs (inspection test plan), follow-up of construction contracts from a QC point of view (contractual charts, KPIs follow-up, periodic reporting.), will be highly valued.
- You are fluent in English (at least C1).
- Knowledge or experience in Regulatory Compliance will be highly valued, ideally in Chemicals, Oil & Gas industry and Blue & Green energy generation projects.
- Desirable: familiar with Project Certification Plant and working knowledge of EU Directives (PED, Welding, NDT's and Machine, ATEX,.).
Additional information:
- Flexible schedule and 2 days a week working from home.
- 23 days of vacation.
- Personalized flexible remuneration program.
- Possibility of national and international mobility within the Group offices.
- Applications that have a certificate of disability will be considered.
- Only applications that have permission to work in Spain will be considered.
As an equal opportunity employer Technip Energies considers only qualified applicants without regard to colour, age, race, ethnicity, sexual orientation, gender expression, disability, national origin, veteran or marital status.
Coordinador / A De Calidad Qa / Qc - Ingeniería Y Construcción (H / M / X) 1906
Hoy
Trabajo visto
Descripción Del Trabajo
En Vithas , seguimos creciendo y apostando por la calidad. Por eso, buscamos un/a Coordinador/a de Calidad que quiera marcar la diferencia en nuestro hospital Vithas Madrid Arturo Soria .
¿Qué te ofrecemos?
- Formar parte de un grupo hospitalario en plena expansión, comprometido con la innovación y la mejora continua.
- Un entorno colaborativo donde tu visión y liderazgo tendrán un impacto directo en la seguridad y satisfacción de nuestros pacientes.
- Jornada completa y un paquete retributivo competitivo , adaptado a tu experiencia y perfil.
- Reportarás directamente a la Gerencia Hospitalaria , trabajando de la mano con equipos multidisciplinares.
Tu misión
Serás el motor del sistema de calidad del hospital, liderando iniciativas clave como:
- Diseño y evaluación de procesos asistenciales y de gestión.
- Implantación de indicadores de calidad y planes de mejora.
- Preparación de auditorías internas y externas (ISO, Joint Commission International.).
- Coordinación de comités clínicos y grupos de trabajo.
- Desarrollo de estrategias alineadas con el Programa de Calidad Corporativo.
Quality Management Lead
Hoy
Trabajo visto
Descripción Del Trabajo
Location: Barcelona (Spain), Romania, Bulgaria, other European locations considered
Reporting to: Vice-president of portfolio and IP
Why This Role Rocks:
Be at the heart of innovation in a pharma company blending generics and breakthrough drugs.
Own the European IP strategy. Your work directly shapes market access and portfolio success.
Work with a dynamic, global team bridging IP, Regulatory, and Business Development.
Lead high-stakes patent challenges, oppositions, and new filings. Make your mark!
Guide and support team members, contributing to their development and success.
Who You Are:
European Patent Attorney (or almost there) with 5–10+ years in pharma patents.
Confident navigating complex European IP landscapes, FTO, SPCs, and exclusivities.
Analytical, hands-on, structured. You love solving tough IP puzzles.
Fluent in English, curious about other languages, and thrive in multicultural teams.
Your Mission:
Assess Freedom to Operate and unlock routes to market.
Lead oppositions, appeals, and patent lifecycle management in Europe.
Protect innovation;
spot opportunities, draft new filings, and monitor competitors.
Be the trusted IP advisor for Regulatory, Licensing, and Business Development teams.
Manage trademarks and brand IP with a strategic mindset.
Why You’ll Love It:
High-impact role where your decisions matter globally.
Opportunity to grow in a fast-paced, international company.
Real strategic ownership. Your fingerprints on every key project.
About Lotus
Lotus is an international pharmaceutical company with a global presence, focused on
commercializing both novel and generic pharmaceuticals. Founded in Taiwan and recognized for its robust R&D and manufacturing platform in Asia, Lotus combines focused in-house capabilities with a network of partners to ensure a competitive advantage through enhanced speed and flexibility. The company delivers a diverse portfolio of high-quality, affordable medicines to markets worldwide.
Sap Quality Management Consultant
Hoy
Trabajo visto
Descripción Del Trabajo
En pocas palabras
Posición: Consultor SAP QM Senior
Localización: Madrid, modalidad híbrida
Experiencia: Más de 5 años como consultor SAP
¿Quieres saber más?
INSUD PHARMA es un referente global en el sector farmacéutico, comprometido con la innovación y la excelencia operacional en la cadena de valor farmacéutica. Actualmente lideramos un proyecto global para la implantación y migración de nuestro sistema SAP ECC a SAP S4/HANA. Buscamos un Consultor SAP QM con experiencia para colaborar en esta transformación, asegurando la calidad y la correcta ejecución del proyecto en su área de conocimiento.
¿Qué buscamos?
- Colaborar en la implantación y migración de SAP S4/HANA, trabajando junto con colaboradores externos y usuarios clave.
- Analizar, supervisar y proporcionar soluciones para garantizar la calidad y adherencia al Core Model definido para INSUD PHARMA.
- Gestionar requisitos de usuarios, analizar su viabilidad y configurar soluciones SAP de acuerdo al modelo core.
- Desarrollar, implementar y validar protocolos de prueba para nuevos desarrollos y correcciones.
- Asesorar y formar a usuarios para optimizar el uso del sistema SAP QM.
- Elaborar documentación técnica de análisis, diseño, pruebas y formación según metodología del departamento.
- Monitorizar la calidad de los procesos financieros alineados con las mejores prácticas SAP.
¿Qué necesitas?
Sap Quality Management Consultant
Hoy
Trabajo visto
Descripción Del Trabajo
formación PMP deseable.Fluidez en español e inglés deseable. Más de 5 años de experiencia como consultor SAP, valorándose experiencia en industria farmacéutica. Conocimientos profundos en SAP QM: Quality Planning, Quality Inspection, Quality Control, Certificates, Stability Studies Experiencia en proyectos de implantación SAP S4/HANA y rol de roll-outs internacionales. Valorable conocimiento en módulos SAP MM, EWM y PP. ¿Cómo será el proceso de Selección? ️ Contacto inicial telefónico o vía correo electrónico. 1 o 2 entrevistas, presenciales o virtuales. Información continua sobre el estado del proceso. ¿Crees que esta oferta no es para ti? Síguenos en LinkedIn e Instagram para conocer más oportunidades. InsudPharma Challenger InsudTalent COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En INSUD PHARMA promovemos la igualdad de género y no discriminación por razones de etnia, religión, orientación sexual, discapacidad u otras condiciones personales o sociales. Fomentamos un entorno inclusivo y diverso para todos nuestros colaboradores.
Sap Quality Management Consultant
Hoy
Trabajo visto
Descripción Del Trabajo
En pocas palabras
Posición: Consultor SAP QM Senior
Localización: Madrid, modalidad híbrida
Experiencia: Más de 5 años como consultor SAP
¿Quieres saber más?
INSUD PHARMA es un referente global en el sector farmacéutico, comprometido con la innovación y la excelencia operacional en la cadena de valor farmacéutica. Actualmente lideramos un proyecto global para la implantación y migración de nuestro sistema SAP ECC a SAP S4/HANA. Buscamos un Consultor SAP QM con experiencia para colaborar en esta transformación, asegurando la calidad y la correcta ejecución del proyecto en su área de conocimiento.
¿Qué buscamos?
- Colaborar en la implantación y migración de SAP S4/HANA, trabajando junto con colaboradores externos y usuarios clave.
- Analizar, supervisar y proporcionar soluciones para garantizar la calidad y adherencia al Core Model definido para INSUD PHARMA.
- Gestionar requisitos de usuarios, analizar su viabilidad y configurar soluciones SAP de acuerdo al modelo core.
- Desarrollar, implementar y validar protocolos de prueba para nuevos desarrollos y correcciones.
- Asesorar y formar a usuarios para optimizar el uso del sistema SAP QM.
- Elaborar documentación técnica de análisis, diseño, pruebas y formación según metodología del departamento.
- Monitorizar la calidad de los procesos financieros alineados con las mejores prácticas SAP.
¿Qué necesitas?
Director Quality Management (M/W/D)
Hoy
Trabajo visto
Descripción Del Trabajo
Responsibilities Lead the Global Clinical Team (GCT) and represent Clinical Development on the Global Program Team (GPT).
May serve as the Clinical Development Representative on NIBR clinical/project teams to drive transition of pre-PoC (Proof of Concept) projects to Development Decision Point (DDP).
Develop an endorsed Integrated Development Plan (IDP) aligned with the Target Product Profile (TPP) to support global regulatory approval and market access for one or more indications or programs.
Support registration, market access, commercialization, and maintenance of product licenses.
Collaborate with Patient Safety to ensure continuous evaluation of the drug safety profile and conduct safety monitoring of clinical studies;
serve as a core member of the Safety Management Team (SMT).
Engage with external stakeholders (regulatory authorities, key opinion leaders, data monitoring committees, advisory boards, patient advocacy groups) and internal stakeholders (Research, Translational Medicine, Global Medical Affairs, Marketing, Health Economics & Outcomes Research) and participate in internal decision boards.
PhD (preferred).
5 years) experience in clinical development within the Nephrology therapeutic area.
Advanced knowledge of the assigned therapeutic area with ability to innovate in clinical development study designs and to interpret and present trial or program-level data.
Demonstrated ability to establish strong scientific partnerships with key stakeholders and proven leadership in delivering high-quality projects/submissions/trials in a global/matrix environment (including remote).
This is a hybrid role which can be based in Basel, London, Dublin, Barcelona or Madrid.
Novartis : Our work helps people with disease and their families.
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Quality Control & Quality Assurance Specialist
Publicado hace 10 días
Trabajo visto
Descripción Del Trabajo
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.
We are currently seeking a dedicated and motivated Quality Control & Quality Assurance Specialist to support a major pharmaceutical project focused on quality control and quality assurance activities within a GxP-regulated environment.
The consultant will work onsite in Madrid until February, directly involved in operational and documentation-related tasks, and will then continue in hybrid mode from our headquarters or remotely.
Please note: Full onsite until February 2026 for this project's duration; hybrid mode following that (remote and/or from our main office)
Responsibilities include, but are not limited to:
- Execute, review, and coordinate all quality control activities related to the microbiological qualification of classified areas .
- Support analytical method validation , including drafting and reviewing related protocols and reports.
- Maintain, update, and review GxP documentation to ensure full compliance with applicable regulations and internal standards.
- Provide support for utilities qualification and other system qualification activities.
- Contribute to the implementation and validation of computerized systems within the ongoing project.
- Collaborate with technical and QA teams to ensure full alignment with established quality procedures.
Required Qualifications:
- Degree in Pharmacy, Chemistry, Biotechnology, Engineering , or related scientific disciplines.
- Minimum of 2 years of experience in Quality Control, Quality Assurance, or Validation roles within the pharmaceutical or biotech industry .
- Strong knowledge of GMP/GxP regulations and qualification/validation guidelines.
- Proven ability to manage, review, and write technical documentation in a regulated environment.
- Excellent organizational and communication skills.
- Fluent Spanish and good command of technical English are required.
Next Steps
Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview.
If there's a positive match, a technical interview with the Hiring Manager will be arranged.
In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal.
Alternatively, if the outcome is negative, we will contact you to halt the recruitment process.
Working at PQE Group
As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you.
Apply now and take the first step towards an amazing future with us.
Quality Control & Quality Assurance Specialist
Hoy
Trabajo visto
Descripción Del Trabajo
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.
We are currently seeking a dedicated and motivated Quality Control & Quality Assurance Specialist to support a major pharmaceutical project focused on quality control and quality assurance activities within a GxP-regulated environment.
The consultant will work onsite in Madrid until February, directly involved in operational and documentation-related tasks, and will then continue in hybrid mode from our headquarters or remotely.
Please note: Full onsite until February 2026 for this project's duration; hybrid mode following that (remote and/or from our main office)
Responsibilities include, but are not limited to:
- Execute, review, and coordinate all quality control activities related to the microbiological qualification of classified areas .
- Support analytical method validation , including drafting and reviewing related protocols and reports.
- Maintain, update, and review GxP documentation to ensure full compliance with applicable regulations and internal standards.
- Provide support for utilities qualification and other system qualification activities.
- Contribute to the implementation and validation of computerized systems within the ongoing project.
- Collaborate with technical and QA teams to ensure full alignment with established quality procedures.
Required Qualifications:
- Degree in Pharmacy, Chemistry, Biotechnology, Engineering , or related scientific disciplines.
- Minimum of 2 years of experience in Quality Control, Quality Assurance, or Validation roles within the pharmaceutical or biotech industry .
- Strong knowledge of GMP/GxP regulations and qualification/validation guidelines.
- Proven ability to manage, review, and write technical documentation in a regulated environment.
- Excellent organizational and communication skills.
- Fluent Spanish and good command of technical English are required.
Next Steps
Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview.
If there's a positive match, a technical interview with the Hiring Manager will be arranged.
In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal.
Alternatively, if the outcome is negative, we will contact you to halt the recruitment process.
Working at PQE Group
As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you.
Apply now and take the first step towards an amazing future with us.
Quality Control & Quality Assurance Specialist
Hoy
Trabajo visto
Descripción Del Trabajo
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.
We are currently seeking a dedicated and motivated Quality Control & Quality Assurance Specialist to support a major pharmaceutical project focused on quality control and quality assurance activities within a GxP-regulated environment.
The consultant will work onsite in Madrid until February, directly involved in operational and documentation-related tasks, and will then continue in hybrid mode from our headquarters or remotely.
Please note: Full onsite until February 2026 for this project's duration;
hybrid mode following that (remote and/or from our main office)
Responsibilities include, but are not limited to:
- Execute, review, and coordinate all quality control activities related to the microbiological qualification of classified areas .
- Support analytical method validation , including drafting and reviewing related protocols and reports.
- Maintain, update, and review GxP documentation to ensure full compliance with applicable regulations and internal standards.
- Provide support for utilities qualification and other system qualification activities.
- Contribute to the implementation and validation of computerized systems within the ongoing project.
- Collaborate with technical and QA teams to ensure full alignment with established quality procedures.
Required Qualifications:
- Degree in Pharmacy, Chemistry, Biotechnology, Engineering , or related scientific disciplines.
- Minimum of 2 years of experience in Quality Control, Quality Assurance, or Validation roles within the pharmaceutical or biotech industry .
- Strong knowledge of GMP/GxP regulations and qualification/validation guidelines.
- Proven ability to manage, review, and write technical documentation in a regulated environment.
- Excellent organizational and communication skills.
- Fluent Spanish and good command of technical English are required.
Next Steps
Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview.
If there's a positive match, a technical interview with the Hiring Manager will be arranged.
In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal.
Alternatively, if the outcome is negative, we will contact you to halt the recruitment process.
Working at PQE Group
As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you.
Apply now and take the first step towards an amazing future with us.