Responsable de obrador - Esferic Group - Sant Cugat del Vallès

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. At Global Regulatory Affairs our aspiration is to be the world's best Regulatory organization, championing patient access to the world's best diagnostics. Focus of our work is the global approval of in-vitro-diagnostics of the Elecsys Core reagent immunoassay product portfolio. Our dynamic team manages regulatory projects as well as overarching regulatory topics. Join an open-minded work environment where close collaboration with colleagues across various departments and countries is not just encouraged, but essential. • Shape Strategic Direction: You will steer the strategic direction and represent the Regulatory Affairs department in international, interdisciplinary teams to foster an effective and successful working environment, • Manage Global Product Registrations: You will manage product registrations across Europe, the United States, and China, while supporting broader worldwide registration efforts, • Act as a Key Interface: You will prepare and submit pre-market applications to the FDA or Notified Bodies, serving as the primary liaison to global health authorities, • Drive Authority Interaction: You will actively interact with regulatory bodies to accelerate approvals or clearances for upcoming registrations and professionally address inquiries of all kinds, • Ensure Portfolio Excellence: You will support product maintenance activities and continuously keep the technical documentation of our product portfolio up to date, • Leverage International Synergies: To achieve efficient global approvals, you will collaborate closely with colleagues in Germany, Switzerland, and the US—both intra-departmentally and with global Regulatory Affairs teams You bring a sophisticated blend of scientific insights and regulatory acumen, coupled with a passion for collaborating across borders to overcome complex healthcare challenges. • Education: A Bachelor's or Master's degree in Life Sciences, Data Science, or a related field, • Professional Experience: A minimum of 5 years of experience within Regulatory, R&D, Quality, Operations, or Clinical environments, • Expertise: Strong technical understanding of IVDs, combined with knowledge of international regulations governing IVD development, manufacturing, and registration (specifically EU, US, and China), • Mindset & Skills: Proven track record in agile project management, exceptional self-organization, and the ability to effectively balance and prioritize multiple overlapping projects, • Language Skills: Excellent command of English (written and spoken) for daily global collaboration; fluency in any additional language is an advantage Locations: Penzberg (Germany), Mannheim (Germany) or Sant Cugat (Spain) At the Company's discretion, an exception to the location requirement could be made. Employment Type: Full-Time; Temporary for 18 months (parental leave replacement) Bei Global Regulatory Affairs ist es unser Anspruch, die weltweit beste Regulatory-Organisation zu sein und den Patientenzugang zu den weltweit besten Diagnostika zu fördern. Der Fokus unserer Arbeit liegt auf der globalen Zulassung von In-vitro-Diagnostika des Elecsys Core Reagents Immunoassay-Produktportfolios. Unser dynamisches Team managt sowohl Regulatory-Projekte als auch übergreifende Regulatory-Themen. Werde Teil eines Open-Minded-Arbeitsumfelds, in dem die enge Zusammenarbeit mit Kolleginnen und Kollegen über verschiedene Abteilungen und Länder hinweg nicht nur gefördert wird, sondern essentiell ist. • Strategische Ausrichtung gestalten: Du steuerst die strategische Ausrichtung und vertrittst den Bereich Regulatory Affairs in internationalen sowie interdisziplinären Teams, um ein effektives und erfolgreiches Arbeitsumfeld zu schaffen, • Globale Produktregistrierungen steuern: Du verwaltest Produktregistrierungen in Europa, den Vereinigten Staaten und China und unterstützt weltweite Registrierungen, • Zentrale Schnittstelle sein: Du bereitest Anträge vor der Markteinführung vor, reichst diese bei der FDA oder einer Benannten Stelle ein und agierst als wichtigste Schnittstelle zu den Gesundheitsbehörden, • Behördeninteraktion aktiv führen: Du interagierst direkt mit Aufsichtsbehörden, um die Genehmigung oder Freigabe anstehender Registrierungen zu beschleunigen und Anfragen aller Art kompetent zu beantworten, • Portfolio-Exzellenz sichern: Du unterstützt Produktpflegeaktivitäten und hältst die technischen Dokumentationen unseres Produktportfolios kontinuierlich auf dem neuesten Stand, • Internationale Synergien nutzen: Um weltweit effiziente Zulassungen zu erreichen, arbeitest Du eng mit Kolleginnen und Kollegen in Deutschland, der Schweiz und den USA zusammen – sowohl abteilungsübergreifend als auch mit den globalen Regulatory Affairs Teams, insbesondere in China und Japan, • Ausbildung: Ein erfolgreich abgeschlossenes Bachelor- oder Masterstudium in Biowissenschaften, Data Science oder einer verwandten Fachrichtung, • Berufserfahrung: Mindestens 5 Jahre fundierte Erfahrung in den Bereichen Regulatory, R&D, Quality, Operations oder Clinical, • Fachwissen: Tiefgehendes technisches Verständnis von IVDs sowie solide Kenntnisse der internationalen Zulassungsgesetze (EU, USA, China), • Arbeitsweise: Starke Fähigkeiten im agilen Projektmanagement, ausgeprägte Selbstorganisation und das Talent, mehrere Prioritäten gleichzeitig erfolgreich zu jonglieren, • Sprachkenntnisse: Exzellente Englischkenntnisse in Wort und Schrift für die tägliche Zusammenarbeit in globalen Teams; jede weitere Sprache ist ein Plus Standorte: Penzberg (Deutschland), Mannheim (Deutschland) oder Sant Cugat (Spanien) – Nach Ermessen des Unternehmens kann eine Ausnahme von der Standortanforderung gemacht werden. Anstellungsart: Vollzeit; Befristet für 18 Monate (Elternzeitvertretung) Dort, wo Entgelttransparenz vorgeschrieben ist, geben wir die Informationen basierend auf dem Hauptstandort der Stelle an. Für diese Position ist der Hauptstandort Penzberg. Falls Du dich für einen anderen Standort interessierst, an denen die Stelle möglicherweise ebenfalls verfügbar ist, geben wir Dir die entsprechenden Entgeltinformationen im weiteren Verlauf des Bewerbungsprozesses. Your contact to us! With people. For people. Do you need further support? Please have a look at our FAQs, you will find them via https://careers.roche.com/global/en/faq. A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer. #J-18808-Ljbffr

This role is responsible for independently developing operational and project strategies in PDM, handling x-functional topics and leading large cross-functional project teams while owning complex strategic supply chain projects. The role leads supply chain strategy development, consults with business executives on high-level supply chain issues, and collaborates with key stakeholders to optimize solutions. The role leverages industry expertise for innovative ideas, and contributes to the development of new frameworks and tools in supply chain projects. This role is responsible for independently developing operational and project strategies in PDM, handling x-functional topics and leading large cross-functional project teams while owning complex strategic supply chain projects. The role leads supply chain strategy development, consults with business executives on high-level supply chain issues, and collaborates with key stakeholders to optimize solutions. The role leverages industry expertise for innovative ideas, and contributes to the development of new frameworks and tools in supply chain projects. • Experience in Product Master data management processes and tools in HP. Master data topics like product lifecycle dates, hierarchy, BOM structure & governance, planning attributes, etc., • Program management and communication skills – self-starter, ability to independently manage multiple initiatives working with x-functional teams, structure governance, • Enterprise applications & tools: includes MS4, S4, Pulsar, costing tools, PLC systems, BI solutions used in the PDM environment, CPQ (config and pricing tools), • Works with key stakeholders as required to optimize supply chain solutions and provide input into new process capability requirements, driving an improved implementation experience and high adoption rate., • Leads large, cross-functional project teams, providing mentoring and guidance to achieve project goals., • Interprets benchmarking and statistical data to create new processes, strategies, and tools to be used for supply chain business objectives., • Four-year or Graduate Degree in Supply Chain Management, Manufacturing Engineering, Operations management, Business Administration, or any other related discipline or commensurate work experience or demonstrated competence., • Typically has 10+ years of work experience, preferably in supply chain, operations, or a related field., • Network with relevant PDM stakeholders in PS GBU, marketing, planning, procurement, planning fulfilment, • Knowledge of industry standard PLM tools like Windchill This job description describes the general nature and level of work performed in this role. It is not intended to be an exhaustive list of all duties, skills, responsibilities, knowledge, etc. These may be subject to change and additional functions may be assigned as needed by management. Supply Chain & Operations Full time No shift premium (Spain) HP, Inc. provides equal employment opportunity to all employees and prospective employees, without regard to race, color, religion, sex, national origin, ancestry, citizenship, sexual orientation, age, disability, or status as a protected veteran, marital status, familial status, physical or mental disability, medical condition, pregnancy, genetic predisposition or carrier status, uniformed service status, political affiliation or any other characteristic protected by applicable national, federal, state, and local law(s). Please be assured that you will not be subject to any adverse treatment if you choose to disclose the information requested. This information is provided voluntarily. The information obtained will be kept in strict confidence. For more information, review HP’s EEO Policy or read about your rights as an applicant under the law here: “Know Your Rights: Workplace Discrimination is Illegal" #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position At Roche, we believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives and we are brave in both decision and action. And we believe that good business means a better world. Join Our Team: Make a Difference in International Regulatory Affairs! Roche is seeking a dynamic and highly motivated individual to join our team as an International Regulatory Affairs Professional. We are looking for candidates who bring an innovative and creative mindset to the table, along with a proven track record in the Regulatory Affairs field. If you are passionate about making a positive impact on global healthcare through regulatory excellence, we invite you to be part of our dedicated team. Key Responsibilities As an International Regulatory Affairs Professional at Roche, you will be responsible for: - Leading and supporting regulatory strategies for global IVD/MD instruments and software submissions - Ensuring compliance with international regulatory requirements and standards - Collaborating with cross-functional teams, including R&D, Quality, and Clinical, to drive regulatory initiatives - Providing regulatory guidance to support product development and lifecycle management - Staying abreast of evolving regulatory trends and up‐ dates, and implementing best practices Requirements - Bachelor’s Degree in Life Sciences, Regulatory Affairs, or a related field - 5 to 7 years of experience in Regulatory Affairs ( Regulatory, R&D, Quality and/or Clinical), with some experience in healthcare regulatory affairs - In-depth knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments & software - Strong organizational and communication skills - Ability to multitask and effectively manage multiple projects simultaneously - Self-motivated and capable of working independently in a self-management environment - Experience in IVD instrument and/or software development Why Roche - Collaborative and innovative work environment - Opportunity to make a meaningful impact on patients' lives globally - Competitive compensation and benefits package - Professional development and growth opportunities within a leading global healthcare organization If you are a dedicated professional who thrives in a fast-paced environment and is passionate about contributing to the International Regulatory Affairs landscape, we want to hear from you! Submit your resume and cover letter detailing your relevant experience and qualifications. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

HP is seeking a Data Product Manager to craft personalized customer experiences by leveraging real-time data across HP Smart ecosystems. ¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura hoy mismo. You will drive data products, collaborate with engineering, product and marketing, and apply AI to automate insights and experiences, while upholding privacy policies. xqbhyrx Join a cross-functional team focused on scalable data-driven customer engagement and global rollout, blending analytics with strategic product growth. #J-18808-Ljbffr

HP is seeking an experienced Senior Analytics Consultant to join the Sales Compensation Insights & Analytics organization. ¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad. You will design analytical frameworks, partner with stakeholders, and translate business needs into scalable data solutions. You will lead cross-functional discussions, influence senior leaders, and deliver data-driven insights to shape strategic decisions. The xqbhyrx role emphasizes analytics, forecasting, and performance measurement, with close collaboration across business and #J-18808-Ljbffr

The Position Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. As an Environmental Regulatory Compliance Manager, you will lead the implementation of evolving product environmental and sustainability regulations (such as REACH, Biocides, PFAS, and more). Your mission is to ensure Roche Diagnostics products are globally compliant and managed with excellence. You will define how compliance looks for our portfolio, future‑proofing our products and ensuring the organization is ready for audits and regulatory authorities. Your Main Responsibilities • Detailed Regulatory Assessment: Oversee the technical evaluation of new regulations, providing clear, auditable interpretations and rationales, identifying risks early and designing mitigation strategies., • Strategic Compliance Roadmap: Identify upcoming regulatory trends and define long‑term strategies to protect the Roche portfolio., • Program Management & Prioritization: Manage multiple complex projects, ensuring priorities are set to implement regulations efficiently across the organization., • Stakeholder Engagement: Act as the internal point of contact and expert for senior leaders and cross‑functional teams, translating complex legal text into actionable business insights., • Standardization & Frameworks: Lead harmonization of assessment processes, creating repeatable and adaptable frameworks for the Diagnostics division., • KPIs & Reporting: Maintain a clear overview of compliance status per regulation, reporting progress and milestones to ensure full transparency. Who You Are • Scientist‑turned‑Regulator: solid experience in product stewardship or environmental regulations., • Analytical Mindset: evaluate business impact by applying legal text to technical data; implement complex environmental requirements., • Effective Communicator: explain the "why" behind a regulation to both scientists and executives., • Collaborative Leader: excel in matrixed organizations, building high‑performing project teams and communicating data‑driven decisions., • Technical Skills & Languages: fluent in English. Knowledge of SAP EHS/EHS‑M and experience in project management (Waterfall & Agile) are highly valued. What Is Here for You? • A purpose‑driven role that contributes directly to Roche's sustainability and environmental responsibility., • Strategic influence: shape the future of our product portfolio through your interpretations and decisions., • Dynamic environment: work at the intersection of science, law, and business with professional collaboration., • Growth & Innovation: build frameworks from scratch and standardize global processes, offering a platform for professional excellence. Location Primary location: Sant Cugat del Vallès. Pay transparency applies; specific details will be provided during the hiring process. xqbhyrx Equal Opportunity Employer Roche is an Equal Opportunity Employer. #J-18808-Ljbffr