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Lead global product strategy, marketing, and branding for key Cetaphil ranges. Brand/Product roles within skincare, beauty, pharma. Proven experience in product innovation, brand building, and digital‑first marketing.

In a nutshell Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a broad range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value in both human and animal health. Our activities are organized in three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries. We are committed to innovation and sustainable development to deliver solutions that positively impact global health. Ready to be a #Challenger at INSUD PHARMA? What are we looking for? We are seeking a Regulatory Affairs Manager to lead the regulatory strategy for our innovative and biosimilar products, ensuring compliance and collaborating with global, cross-functional teams. Key Responsibilities: • Monitor changes in the regulatory landscape, identify their impact, and propose solutions to maintain compliance., • Define regulatory strategy for each product in coordination with Management and Business teams., • Build strong collaborative partnerships with internal and external teams to ensure organizational success and patient safety., • Identify and mitigate regulatory risks, adapting strategies to evolving regulations and Health Authority feedback., • Interpret and communicate legislative changes that affect product registration, manufacturing, or development., • Support the review of license and quality agreements for targeted geographies., • Lead engagement with Health Authorities during Scientific Advice procedures and responses to deficiency letters., • Prepare, review, and approve regulatory submission documents (briefing packages, IBs, INDs, CTAs, MAAs, etc.)., • Manage external consultants and vendors for regulatory activities., • Support product launch activities, ensuring regulatory risks are managed with appropriate action plans., • Organize the regulatory submission schedule and coordinate with Regulatory Affairs teams., • Participate in product plan development, regulatory strategy, and CMC documentation., • Drive digitalization and the use of computerized systems within the department. The challenge!

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that is bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth and variety in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We hire the best and trust them from day 1 to deliver global impact, handle teams and be responsible for the outcomes while our leaders support and mentor you. We are a profitable rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of these will lead to a truly differentiated experience for you. If this excites you, then apply below. Content Coordinator – Global Content Operations Location – Spain Remote You will be responsible for: • Act as the primary liaison for content submissions from internal teams and external agencies., • Managing end-to-end content intake, validation, and preparation for submission., • Coordinating across medical, brand, regulatory/legal, and agency teams to ensure timely progression of content., • Monitoring jobs through all workflow stages and resolving blockers or routing issues., • Assist in managing content calendars and supporting campaign execution across channels., • Tracking global content timelines across franchises, identifying potential bottlenecks before SLA breaches, and reporting progress to Commercial Excellence teams., • Acting as a coordination point between content owners, agencies, and DAM librarians to align on quality control expectations and operational workflows., • Supporting onboarding of external agencies on franchise-specific PromoMats processes and ensuring appropriate system access and governance from the start., • Supporting lifecycle management including version control, renewals, expirations, and archival of content assets., • Tracking global-to-local content adaptation across markets and supporting insights that inform content reuse and evolution guidelines., • Maintaining content trackers, dashboards, and SLA-based performance reporting., • Contributing to the continuous improvement of content operations processes, templates, and workflow governance., • Supporting scalable content operations by enabling structured content, reuse, and governance practices that improve global content efficiency across franchises., • Support change management activities related to new processes, templates, or system enhancements., • Identify opportunities to improve operational efficiency and content reuse., • A seasoned content operations professional with 12+ years of strong experience in pharma or life sciences., • Background in managing large volumes of medical/promotional content within structured, regulated environments., • Deep familiarity with Veeva systems (PromoMats, DAM) and end‐to‐end content lifecycle processes., • Proven ability to coordinate multiple stakeholders across global and local teams., • Strong understanding of claims, references, compliance, and medical review processes., • Highly organized, detail‐oriented, and capable of managing simultaneous submissions under strict timelines., • Comfortable working in a complex global ecosystem with multiple agencies and cross‐functional partners., • Demonstrates strong communication, follow‐up, and operational ownership., • Understanding of structured content, modular content, taxonomy, and metadata frameworks., • Strong project coordination and workflow management capabilities., • Ability to maintain accurate trackers, dashboards, and SLA reporting., • Skilled in content lifecycle management (intake → review → approval → publish → archive). Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate's merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

pCognizant Company is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. /ppbr/ppbAbout the role: /b /ppWe are seeking an IT Project Engineer who play a key role in a large-scale Windows Security Patching program for a pharmaceutical client, the project is transitioning from delivery to steady-state operations. We are looking for a M2O Coordinator to own and drive this transition, ensuring all processes, documentation, and governance are in place for a seamless handover. /ppbr/ppbResponsibilities: /b /ppbr/pulliDefine and execute the Move-to-Operation strategic plan (process, people, tools, governance). /li /ulp• Design the target operating model: roles, escalation paths, SLA/KPI framework. /pp• Prepare and present weekly status updates to stakeholders (progress, risks, blockers). /pp• Document all operational processes in compliance with CFR 21 Part 11 and GxP standards. /pp• Coordinate the knowledge transfer and training plan for the operations team. /pp• Define cutover strategy and hypercare period with clear entry/exit criteria. /ppbr/ppRequirements: /ppbr/pp• Strong knowledge of pharmaceutical and manufacturing systems /pp• Bachelor’s degree (preferred) /pp• 3–5 years in IT service transition, project coordination, or IT operations in a regulated environment. /pp• Solid knowledge of ITIL v3/v4 (Service Transition, Continual Improvement). /pp• Familiarity with CFR 21 Part 11: electronic records, audit trails, data integrity (ALCOA+). /pp• Experience with project management tools (MS Project, Jira, ServiceNow or equivalent). /pp• Excellent communication and presentation skills; structured and methodical approach. /pp• English fluent (mandatory); French is a plus. /pp• Strong written communication and process improvement skills /ppPreferred qualification: ITIL v3/v4 Foundation (minimum), PMP, PRINCE2, or equivalent. /ppbAbout Cognizant /b /ppCognizant (Nasdaq-100: CTSH) is one of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant is ranked 185 on the Fortune 500 and is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with or follow us @Cognizant. /p

pTake your career to the next level with Amaris Consulting as a bValidation Specialist (Test QA) /b. Become part of an international team, thrive in a global group with €800M turnover and 1,000+ clients worldwide, and an agile environment by planning the kickoff and follow up on projects. Join Amaris Consulting, where you can develop your potential and make a difference within the company. /ppbr/ppbWHAT WOULD YOU NEED? ✍️ /b /pulli+3 years of senior experience in IT validation within GxP environments /liliProven expertise in bVeeva Conformance and Validation Testing /b and bW3C Validation /b /liliStrong knowledge of pharma industry regulations and GxP compliance /liliExperience with LeVA system life cycle documentation (VP, URS, FS, RA, Testing Reports, AAP) /liliDegree in Business Administration, Computer Science or comparable professional experience /lilibEnglish fluency /b and Spanish as mother tongue is highly valued /li /ulpbr/ppb WHAT WILL YOU DO? /b /pulliLead validation activities for global testing applications (BI-AS-ODIN, BI-IT-INMATION) /liliEnsure compliance with validation planning and applicable BI standards before system operation /liliDevelop and maintain system-specific SOPs and SLC documentation /liliManage validation status throughout system lifecycle and post-operation phases /liliCreate and deliver training on Standard Operating Procedures as defined in Validation Plans /liliCoordinate with IT Operations Laboratories teams on Manufacturing Connectivity projects /li /ulpbr/ppb /p /b

pAt bAstek /b, we are looking for a bSenior IT Project Manager /b to join a high-impact international initiative with one of our key partners in the bpharmaceutical industry /b. /ppYou will be part of a bglobal program /b with teams distributed across bEurope, the US, and China /b, collaborating with multiple IT and business stakeholders in a highly regulated environment (Pharma RD). /ppbr/pp bMain Responsibilities /b /pulliCoordinate project timelines, deliverables, and financial activities across multiple RD IT systems /liliSupport the execution of system changes aligned with program objectives /liliAct as a primary point of contact for global stakeholders (EU/US/Asia) /liliEnsure alignment and communication across distributed teams /liliPrepare program-level reports (status, risks, dependencies, progress) /liliAnticipate risks, propose mitigation strategies, and drive resolution /liliContribute to governance activities and continuous improvement within the program /li /ulpbr/pp bWho You Are /b /pullib5+ years /b of experience managing IT projects in international or multicultural environments /liliExperience in bPharma, Life Sciences, Biotech, or regulated environments (highly valued) /b /liliProject Management certifications (bPMP /b or bPRINCE2 Practitioner /b) /liliSolid understanding of bWaterfall /b and bAgile /b methodologies (Scrum, Kanban) /liliKnowledge of bITIL /b and IT Service Delivery practices /liliHands-on experience with tools such as bServiceNow (SNOW) /b, bHPSM /b, bJira /b /liliExposure to bRelease / Change Management /b processes /liliExcellent communication and stakeholder management skills /lilibEnglish C1/C2 /b (global environment) /liliAvailability to travel if required /li /ulpbr/pp bWhy Join Us? /b /ppbr/pulli /ul /li

At Astek, we are seeking a SAT Tester to collaborate with our partner in the pharmaceutical industry in an international setting Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto. Your mission, should you choose to accept it… • Design and execute System Acceptance Tests (SAT) in GxP environments., • Perform both manual and automated testing., • Ensure traceability between requirements, test cases, and results., • Identify, document, and track defects., • Collaborate with validation teams to ensure compliance with regulatory standards., • Contribute to the testing strategy and the continuous improvement of testing processes. Who are you? We are looking for someone with the following knowledge and experience: • Solid experience in testing and validation within the pharmaceutical industry., • Experience in manual and automated testing., • Knowledge of GxP and the validation lifecycle., • Familiarity with test automation tools (e.g., Selenium, Cypress, or equivalents)., • Experience with CI/CD pipelines., • Knowledge of CSV and validation documentation., • Fluency in English and strong collaboration skills in international teams Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? You will grow professionally in a company in constant development and evolution. You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. You will make a real contribution to the company's development in real time. You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. You will join our team: diverse, multicultural and constantly growing. You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! Shall we meet? xcskxlj If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

Astek is looking for a Senior Scrum Master to work with our partner in the pharmaceutical sector, supporting agile delivery and fostering high-performing teams while driving digital transformation in an international environment. Por favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación. Who are you? We are looking for someone with the following knowledge and experience: • 5–6 years of experience working in Agile environments, with at least 3–4 years as a Scrum Master, • Solid experience applying Scrum principles and facilitating agile ceremonies (Sprint Planning, Daily, Review, Retrospective), • Ex7erience working with multiple Scrum teams simultaneously in complex environments, • Previous experience in large or regulated organizations (pharma, healthcare, finance, etc.), • Experience using agile tools such as Jira and Confluence, • Strong facilitation, coaching, and stakeholder management skills, • Ability to identify and remove impediments and help teams continuously improve, • Experience working with frameworks such as Kanban or scaled environments like SAFe is a plus, • Scrum certifications such as Professional Scrum Master (PSM) or Certified ScrumMaster (CSM) are considered an advantage Who are you? We are looking for someone with the following knowledge and experience: • 5–6 years of experience working in Agile environments, with at least 3–4 years as a Scrum Master, • Solid experience applying Scrum principles and facilitating agile ceremonies (Sprint Planning, Daily, Review, Retrospective), • Experience working with multiple Scrum teams simultaneously in complex environments, • Previous experience in large or regulated organizations (pharma, healthcare, finance, etc.), • Experience using agile tools such as Jira and Confluence, • Strong facilitation, coaching, and stakeholder management skills, • Ability to identify and remove impediments and help teams continuously improve, • Experience working with frameworks such as Kanban or scaled environments like SAFe is a plus, • Scrum certifications such as Professional Scrum Master (PSM) or Certified ScrumMaster (CSM) are considered an advantage Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? You will grow professionally in a company in constant development and evolution. You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. You will make a real contribution to the company's development in real time. You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. You will join our team: diverse, multicultural and constantly growing. You will have days full of good energy and good atmosphere. ...although you still have a lot to discover! Shall we meet? If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more. xcskxlj Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Cyber Security Engineer, Braine (Belgium), Site Based Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. Cognizant Company is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. About the role: We are seeking an OT Engineer who play a key role in supporting OT Security BAU team within a regulated manufacturing environment. The purpose of the role is to ensure accurate and up-to-date documentation, align procedures across sites, and contribute to overall cyber security governance. The successful candidate will help drive continuous improvement of OT security controls and processes while ensuring compliance with internal standards and regulatory requirements. Responsibilities: • Ensure alignment and harmonization of cyber security procedures across global manufacturing sites., • Contribute to the governance and continuous improvement of OT security controls, including risk assessments and control effectiveness reviews. • Utilize tools such as Veeva or other regulated document management systems to manage documentation workflows in a GMP-compliant manner. • Assist in tracking and reporting progress of ongoing cyber security initiatives and ensuring alignment with the company's cyber security framework and regulatory requirements Requirements: • Strong knowledge of pharmaceutical and manufacturing systems, • Bachelor’s degree (preferred), • Automation Engineering, Information Technology, OT Cyber security, or Automation, • A foundational understanding of engineering or IT principles is essential to interpret and apply OT security standards, compliance frameworks, and technical documentation within regulated manufacturing environments. • Minimum 3 years of experience in OT Cyber security or Automation within GMP-regulated manufacturing., • Hands-on experience with governance processes, SOP development, and regulated documentation systems (e.g., Veeva)., • Familiarity with OT security frameworks (e.g., IEC 62443), network segmentation, and enabling services such as patching, antivirus, and asset inventory., • Demonstrated ability to collaborate cross-functionally with Quality, IT, and Engineering stakeholders, • The position requires an experienced professional capable of operating independently in a regulated environment, ensuring alignment of OT cyber security controls with quality and compliance expectations. Proven knowledge reduces onboarding time and enhances the team’s ability to meet global audit and regulatory requirements. • Proficiency in documentation lifecycle management • Experience with GxP and CFR Part 11 compliance, • Strong written communication and process improvement skills About Cognizant Cognizant (Nasdaq-100: CTSH) is one of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant is ranked 185 on the Fortune 500 and is consistently listed among the most admired companies in the world. xcskxlj Learn how Cognizant helps clients lead with or follow us @Cognizant.

Te interesaría seguir desarrollándote como.Especialista de Cualificaciones y Calibraciones.TÉCNICO/A DE CUALIFICACIONES Y CALIBRACIONES.Cuáles serán tus funciones principales?.URS, documentación del proveedor), con el fin de comprobar la correcta ejecución y finalización del trabajo.DQ, IQ,

Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly focus on Innovation is looking for a Salesforce Technical Lead. Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto. Por favor, asegúrese de consultar la descripción a continuación con atención. MAIN TASKS: • Provide support to the sales and functional team in assigned accounts when technical knowledge of the solution is required: Solution design, estimation, and assumptions., • Support the PM/DM in technical leadership on the project, bringing comprehensive technical knowledge of the platform and identifying the best solution to meet the project's functional demands., • Detect and notify risks in the technical management of project/client profitability., • Ensure the smooth progress of the project in terms of Scope, Schedule, and Costs. Alerting and anticipating possible deviations to the Project Manager/Delivery Manager., • Ensure the fulfillment of the project's technical objectives., • Ensure compliance with the agreed software quality standards with Omega's Technical Management., • Supervise the effort estimations of the development and support team during the testing phase of a project., • Collaborate with the PM/DM in project demos for the client., • Ensure the final delivery of technical documentation for a project., • Participate in the development and training of the technical team, advising them to improve their technical skills., • Identify possible technical Up & Cross Selling opportunities., • Identify possible methodological improvements for the technical team., • Collaborate in Omega's community of practice, providing thought leadership, training, and mentoring to other collaborators to develop technical capabilities. REQUIRED EXPERIENCE: • 3+ years participating in the full lifecycle of implementations., • Experience in projects., • Experience in the different modules: Sales Cloud, Service Cloud, Marketing Cloud,, • Experience with agile methodologies., • Permanent contract., • Flexible Schedule. We make it easy. Balance your professional and personal life., • Certifications plan. Improve your skills and get the official certificate from our main partners., • Home Office. You decide and we support you., • Flexible retribution (public transport ticket, Ticket restaurtant, …)., • Health insurance., • OMEGA in action. Our commitment to a better society is not just an intention Omega CRM, a Merkle Company, is a global digital company specialising in accelerating the Business Experience (BX) of our clients through customer-centric solutions, technology, and data – all enhanced by AI. Together with Merkle, we form the largest Customer Experience Management (CXM) agency in Spain, and as part of the dentsu group, we offer end-to-end solutions that integrate media, creativity, content, technology, and strategy to deliver real business impact. With over 23 years of experience, a team of 580+ professionals from 24 nationalities, and 2,500+ certifications, Omega CRM is a recognised leader in the Salesforce ecosystem in Spain. We operate across key industries including Retail, Healthcare, Pharma, Real Estate, Education, and Non-Profit, delivering omnichannel experiences in Customer Service, eCommerce, Marketing, and Analytics. Client satisfaction is at our core (rating: 4.9/5), and we’ve been recognised with awards such as Salesforce Partner of the Year FY23 and Most Innovative Project (Iberia). At Omega CRM, we believe in growth through people – guided by our values: #Talent, #Flexibility, #Commitment, and #Innovation. xcskxlj We grow #Together.

INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama de principios activos farmacéuticos (API), formas farmacéuticas acabadas (FDF) y p

We are seeking a Project Manager with strong functional and operational understanding of Salesforce Marketing Cloud campaign operations, Veeva CRM workflows, and the end-to-end Closed Loop Marketing (CLM) asset lifecycle within a pharma / life sciences environment. Manage cross-functional stakeholde

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and commercialization of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDF), and branded ph

Ejecutivo de Compras Farmacéuticas Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora.Ubicación preferente: Murcia | Madrid | Valencia Misión del Puesto Liderar la negociación estratégica con laborat

Senior Data Engineer – AI Labs at Insud Pharma. AI Labs is Insud Pharma’s transversal team for. The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and wome

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceuti

Estamos contratando: Medical Writer (Pharma Project) /b /ppbr/pp¿Tienes formación científica y experiencia creando o revisando contenido en la industria farmacéutica? ¿Te interesa trabajar en un entorno internacional donde la calidad, el rigor científico y el impacto en comunicación son cla

Como Customer Control / Customer Manager, tu misión será garantizar el control end‐to‐end de los pedidos de cliente, asegurando la calidad del servicio y una gestión analítica y proactiva del forecast, los tiempos de suministro y los hitos clave del ciclo del pedido. Experiencia en gestión

You will act as a trusted legal partner to Commercial, Regulatory, Quality and Operations teams, handling:. Legal support in a regulated pharma environment. We are hiring a Legal Counsel (Commercial & Corporate) to join an international pharmaceutical company based in Madrid.

Posición: Operario/a de Producción Galénica - I+D.Localización: Azuqueca de Henares.Experiencia: Valorable al menos 3 años en el desempeño de las funciones descritas.INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigaci

Posición: Técnico/a Garantía de Calidad.Localización: Azuqueca de Henares.Experiencia: 2 a 4 años en funciones similares.INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, ven

Demonstrated experience supporting pharma or life sciences omnichannel operations. This role is ideal for someone who is comfortable operating in a pharma environment, with strong data governance sensibilities and the ability to translate business objectives into scalable omnichannel journeys.

Position: Launch Specialist – New Product Introduction (NPI) Location: INSUD PHARMA Headquarters, Sanchinarro (Madrid) – On-site Experience: 3-5 years in project management, preferably in the pharmaceutical industry or regulated sectors Want to know more? INSUD PHARMA operates across the e

Due to a constant growth, PQE is looking for a Junior Pharmaceutical Consultant to support one of our clients in Madrid, Spain. 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 i