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The role will have a major responsibility to mentor junior clinical scientist within Hematology. The role holder may be required to serve as a member of the departmental leadership team, coordinate assets tracking and lead improvement initiatives in service of non\\-drug scorecard objectives.\n\n\nYou will also fulfill the role of a Senior Clinical Scientist assigned to Hematology and in that capacity you are an important part of the project Team, working collaboratively with the program and study level physician or clinical lead as their guide in medical scientific aspects of the compound and its development. The accountabilities are broad however, the core accountabilities are the medical \\& scientific support for the development and implementation of early phase AstraZeneca sponsored clinical program strategy, externally sponsored collaborative research program strategy and studies, including clinical science support for initiating clinical trial(s), protocol/amendment development, IB/DSUR submissions, clinical trial documents, supporting clinical data review, interpretation of the study results and providing/supporting final recommendations to senior management.\n\n\nYou will drive and provide guide input to other non\\-assigned programmes, process improvement initiatives, development of junior clinical scientist within Hematology and provides strategic contributions to the global clinical scientist team. As a key leadership member of the Global Project Team, this position demands strong collaborative communication skills, including the ability to engage with and influence a diverse range of business partners both within and external to AstraZeneca.\n\n\n* Will be required to line lead other Clinical Scientists including project allocations/resource management, recruitment \\& selection, personal development and performance management\n* May be required to serve as the Skills Lead for the Clinical Science group thereby being responsible for ensuring appropriate procedures, training and personal development approaches are in place for the skill group and standard methodology is identified and implemented\n* Contributes to the Departmental Leadership Team to ensure effective ways of working, identification and resolution of issues, departmental objective setting and may extend to prioritization and supervising at the departmental level\n* Will lead or contribute to continuous improvement initiatives\n* May be required to run key alliances (provider and academic) • As required you may be asked to act as Clinical Lead for the program/study or support the clinical lead • Leads or supports clinical input to the clinical development plan at all stages of the programme.\n* Leads or co\\-lead (with Translational and Bioscience Leads) the science\\-to\\-man sub team (TSST) to integrate the biology, translational and clinical science into the programme strategy\n* Leads/supports development of recommendation(s) on further development strategies to internal committees.\n* Leads (or supports, as required) the preparation of clinical and other data for governance and other presentations\n* Provide scientific/medical mentorship to the study team, including the CRO team.\n* Is responsible for the collaboration with the research scientists and translational scientists to provide clinical input to the development and review of data to support development of the pre\\-CDID compounds\n* Follows important developments and trends in the medical \\& scientific literature and disseminates updates to the project team and beyond ensuring all involved parties are aware of key developments and the impact on the strategy\n* Leads the development and review of content and quality of publications and inputs to development of the publication strategy\n* Where required leads project specific reviews of the competitor landscape to advise the program strategy\n* As required, the Group Director Clinical Scientist may be asked to act as Clinical Lead for the AZ sponsored study\n* Guides aspects of the Clinical Development Plan (CDP) and Clinical Study Protocols in keeping with the approved CDP and ensuring linkage of trial data to target product profile\n* Attends (in person or by TC) the Site Initiation Visits, to present the study design and key aspects of the protocol\n* Leads, (or supports as required), clinical data review and interpretation of the study and program level with input from the study or program Physician/Clinical Lead\n* Owns the compilation and interpretation of the data for and from the dose escalation committee/safety review committee, in collaboration with the program physician\n* Leads, approves or provides input for the protocols, amendments, Investigator Brochure, DSURs and other relevant strategic documents. Acts as lead clinical reviewer for Clinical Study Reports\n* Develops and builds investigator and site relationships to support site selection and study start up activities\n* Leads the development and implementation of the externally sponsored collaborative research (ESCR) strategy for a programme. The clinical scientist is the link between the project team and all external clinical research for the programme. For preclinical external research proposals, co\\-leads with the Bioscience Lead.\n* Leads investigator/site relationships for ESCR clinical proposal reviews, protocol review and approval, scientific oversight and discussions for academic basket/umbrella and ESCR studies • Represents the project internally and supports oncology drug development externally as a medical scientific guide with key external collaborators. Supports development of alliances as appropriate.\n* Support due diligence activities for potential in\\-licensing or collaborative opportunities and provides recommendations to senior management\n* Represents AstraZeneca as a support for external meetings such as advisory boards and • Identifies and handles risks within the ESCR portfolio, raises quality issues through the appropriate channels, maintains communications with key AstraZeneca partners as required.\n* Drives key critical initiatives within and beyond the Early Clinical Oncology group • Develops, coaches, mentors, motivates and encourages individuals within the organisation\n* Operates in compliance with GCP and relevant regulatory guidelines.\n\n**Essential Requirements:**\n\n* PhD or Pharm D with at least 10 years experience in the industry\n* Strong Experience working on clinical trials in Hematology \\-Oncology clinical trials experience required.\n* Experience handling and interpreting the results of clinical trials as well as exposure to writing protocols\n* Strong analytical skills\n* Experience of authoring scientific documents\n* Well\\-developed communication skills\n* Sufficient technical and disease area knowledge to be able to interact with confidence with internal and external partner\n* Proven track record of line management","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1758744135000","seoName":"senior-group-director-scientist","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-igualada/cate-product-mgmt-dev1/senior-group-director-scientist-6383924939097712/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"bd4ef360-de7c-4af1-9db9-77d6077997d5","sid":"1e2c8566-95c6-403c-af98-958ac92f1e3d"},"attrParams":{"summary":null,"highLight":["Lead clinical science team in Hematology","Develop and implement clinical strategies","Mentor junior scientists"],"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Barcelona,Catalunya","unit":null}]},"addDate":1758744135866,"categoryName":"Product Management & Development","postCode":null,"secondCateCode":"info-comm-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"isFavorite":false}],"localIds":"10,400","pageTitle":"Product Management & Development in Igualada","topCateCode":"jobs","catePath":"4000,4241,4254","cateName":"Jobs,Information & Communication Technology,Product Management & Development","breadCrumbSeo":{"type":"BreadcrumbList","itemListElement":[{"position":1,"name":"Home","item":"https://es.ok.com/en/city-igualada/","@type":"ListItem"},{"position":2,"name":"Jobs","item":"https://es.ok.com/en/city-igualada/cate-jobs/","@type":"ListItem"},{"position":3,"name":"Information & Communication Technology","item":"https://es.ok.com/en/city-igualada/cate-info-comm-technology/","@type":"ListItem"},{"position":4,"name":"Product Management & Development","item":"http://es.ok.com/en/city-igualada/cate-product-mgmt-dev1/","@type":"ListItem"}],"@type":"BreadcrumbList","@context":"https://schema.org"},"cateCode":"product-mgmt-dev1","total":4,"sortList":[{"sortName":"Best Match","sortId":0},{"sortName":"Newest First","sortId":1}],"hotSearches":["GCC","SUV","Toyota","Petrol","Dubai","AWD","Auto"],"breadCrumb":[{"name":"Home","link":"https://es.ok.com/en/city-igualada/"},{"name":"Jobs","link":"https://es.ok.com/en/city-igualada/cate-jobs/"},{"name":"Information & Communication Technology","link":"https://es.ok.com/en/city-igualada/cate-info-comm-technology/"},{"name":"Product Management & Development","link":null}],"tdk":{"type":"tdk","title":"Igualada Product Management & Development Job Listings - 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Aerospace Structures Engineer Specialist - Additive Manufacturing & UAV Platforms64841267810689120
Indeed
Aerospace Structures Engineer Specialist - Additive Manufacturing & UAV Platforms
**Company Overview:** HPinc is the leader in Additive Manufacturing (3D Printing) next\-generation aerospace drones as a manufacturing solution for high\-performance, mass\-produced Unmanned Aerial Systems (UAS/Drones). We are dedicated to rapid innovation, customer\-focused development, and pushing the boundaries of lightweight, robust aerospace structures. Join our dynamic team and help shape the future of flight. **Job Summary:** We are seeking a highly experienced and motivated Aerospace Structures Engineer with a minimum of 5 years of experience to lead and manage customer\-driven structural development programs for our drone platforms. This critical role focuses on translating customer requirements into scalable, mass\-producible designs optimized using HP leading additive manufacturing (3D printing) technology. The ideal candidate will be the primary technical interface with key customers, guiding projects from concept through final delivery and mass production. **Key Responsibilities:****Customer \& Program Management:*** Serve as the primary technical point of contact for external customers, managing expectations and ensuring clear communication throughout the development lifecycle. * Translate complex customer programs into Statements of Work (SOWs) and operational requirements into detailed, actionable engineering specifications and structural design solutions for drone platforms. * Manage multiple customer development projects, ensuring on\-time delivery, budget adherence, and alignment with certification standards. * Conduct and present detailed technical reviews and progress updates to both internal stakeholders and external customers. **Structures Design \& Analysis:*** Lead detailed design, analysis (FEA), and optimization of primary and secondary drone airframe structures with Ho FEA specialist (e.g., wings, fuselage, rotor components). * Specialization in Design for Additive Manufacturing (DfAM) for light\-weighting and part consolidation. * Validate designs through stress, strain, fatigue, and flutter analysis to ensure compliance with relevant aerospace standards. * Oversee and define requirements for structural testing (coupon, component, and full\-scale) to validate analytical models and designs. **Production \& Quality:*** Collaborate closely with the manufacturing team to industrialize additively manufactured components for repeatable, high\-volume production. * Develop and manage material selection and process specifications unique to aerospace\-grade 3D printed components. * Ensure all structural designs meet strict Mass Production, Cost, and Quality targets while maintaining performance and airworthiness. **Required Qualifications:*** Education: Bachelor's or Master's degree in Aerospace Engineering, Mechanical Engineering, or a closely related field. * Experience: Minimum of 5 years of professional experience i**n aerospace or defense structures design and analysis**. * Additive Manufacturing: Proven, hands\-on experience and expertise in **Design for Additive Manufacturing (DfAM), specifically for structural components**. * Analysis Tools: previos experience in Finite Element Analysis (FEA) software (e.g., ANSYS, NASTRAN/PATRAN) and CAD software (e.g., SolidWorks, CATIA) to lead designers and stress activities. * Aerospace Knowledge: Strong understanding of aerospace materials, failure criteria, and aircraft systems. * Customer Facing: Demonstrated ability to manage complex external customer relationships and technical programs in a fast\-paced environment. **Preferred Qualifications:*** Master degree in aeronautics * Experience with UAS/Drone platform development. * Familiarity with the challenges and solutions for mass production of 3D printed parts. * Knowledge of composite materials design and manufacturing. Impact \& Scope * Impacts multiple teams and may act as a team or project leader providing direction to team activities and facilitates information validation and team decision making process. **Benefits:*** Opportunity to work in an international organization with colleagues coming from all over the world. * Our Women Network organizes activities such as; Networking, the promotion of STEM vocations, talks on: improving business acumen, work life balance and skills of the future etc. * Diverse, continued internal growth and career opportunities. Including HP’s own learning platform and LinkedIn Learning. * An attractive benefit package: + Health \& Life insurance + Lunch at reduced prices at our canteen/ ticket restaurant vouchers + HP product discount + Flex optimization program: Kindergarten tickets, transport discount * Work life balance /flexible working hours * Women, Pride, Young employees, Sustainability and DisAbility! Just a few of our fantastic global business networks you can get involved with locally. * We also dedicate time and resources to contribute with our community through Corporate Volunteering activities, including our onsite HP Charity day * Do you like to give back to the community? Then join one of our many volunteering teams or be a part of the incredible HP charity day held on site annually. * Love sports? Then take advantage of our sports center (indoor and outdoor); gym, squash courts, tennis courts, basketball courts and with 25\+ regular coordinated activities / sports by employees , such as HIIT training, squash, basketball and yoga * We have an onsite Doctor and medical team for our employees, including services such as: nutrition, physiotherapy and general health * Free daily printing Happy hour – from photographs, to large posters. And Hands\-on workshops to print with the latest technology – from wall covers to 3D printed models * Gaming area with HP OMEN’s and Pavilion’s complete gaming line up including Omen gaming chairs and several games both for playing alone, online or multiplayer * A Young employee Network (YEN) which host fun events on a regular basis; such as “beer bust” Fridays at different venues including the beach in the summer time. *ES11*
Carrer d'Elisenda Ribatallada, 11, 08172 Sant Cugat del Vallès, Barcelona, Spain
Senior Unity Core Developer64522510313474121
Indeed
Senior Unity Core Developer
**Team Name:** Unannounced Project**Job Title:** -------------- Senior Unity Core Developer**Requisition ID:** ------------------- R026395**Job Description:** -------------------- At Blizzard, we craft genre\-defining games and legendary worlds for all to share. Through unparalleled creativity and storytelling, we create immersive universes and iconic characters that are beloved across platforms, borders, backgrounds, and generations \- only made possible by building a work environment that nurtures the artistry of game development and unleashes the aspirations of our people. We are currently looking for an enthusiastic and collaboration\-oriented Senior Unity Core Developer to help craft a new, unannounced game. If you are passionate about meaningfully contributing to crafting immersive, intuitive user experiences and delighting players, then this is the ideal role for you. Sound like your next challenge? We can't wait to meet you! **Responsibilities:** ===================== * Work closely, not only with your team and other departments, but also with shared teams, to deliver core technology and tools that enable our teams to produce the best games possible. * Innovate on the tool pipelines. * Act as a service\-oriented ambassador of engineering to the rest of the team, while delivering high\-quality and well\-structured code. * Build, maintain, and improve our systems in existing and new tech stacks (such as Unity ECS/DOTS). * Be a role model with confirmed coding skills, an innovative attitude, and the ability to encourage those around you. * Be proactive and drive your own initiatives. * Be part of the creative journey, actively contribute to the creative process, and then complete it. * Own the code that you create. **Skills to Create Thrills:** ============================= * Extensive software development experience. * Experience in Unity and C\#, in particular at extending the Unity Editor. * Experience crafting and supporting tools used in game development. * Experience with mobile development and the accompanying standard methodologies. * Ability to communicate efficiently with designers and client engineers. * Excellent verbal and written communication skills. * Excellent teamwork skills, flexibility, and ability to balance multiple tasks. * Eagerness to grow and develop yourself. * A passion for games. **Bonus Points:** ----------------- * Experience working with client/server game systems. * Professional experience of runtime performance optimization, ideally on mobile titles. * Experience building a live service and maintaining a live multiplayer game. * Experience with Unity DOTS/ECS or other ECS.
Carrer del Rosselló, 64, Eixample, 08029 Barcelona, Spain
JUNIOR PRODUCT MANAGER - FRENCH (MAN)63839249556481122
Indeed
JUNIOR PRODUCT MANAGER - FRENCH (MAN)
At Mango, we dress everything we do with passion. With roots in Barcelona and presence in over 120 countries, we inspire the world with creativity, innovation, and authenticity. Our multicultural team is the engine behind our success. We take pride in taking fashion further, connecting our unique style with people around the globe. YOUR NEW ROLE: Your goal will be to define and make available to sales points a consistent product offering that meets the needs of each market. YOUR MAIN RESPONSIBILITIES:* You will monitor qualitative and quantitative information. * You will attend buying meetings to provide market feedback. * You will analyze market evolution and short-term forecasts. * You will assign products weekly to your region. * You will optimize country stock levels. * You will set prices during discount periods. * You will manage promotions: proposing models and discounts. * You will conduct competitor analysis. * You will visit various sales points. * You will maintain continuous contact with stores. * You will participate in meetings with different departments. ABOUT YOU:* Degree in Business, ADE, Marketing or similar. * At least 2 years of experience in product management within the retail sector. * Advanced level of French is essential. * Analytical skills and product sensitivity. * Passion for fashion and results-oriented. * Strong communication skills and ability to work in a team. YOUR BENEFITS:* Enjoy a flexible schedule and hybrid work model adapted to your needs. At Mango, we support work-life balance. * At Mango, the weekend starts on Friday at noon. We offer reduced working hours on Fridays and eve of public holidays. * Plan your vacations according to your preferences. At Mango, we value your time and want you to enjoy every moment. * As part of the Mango team, you will receive a 35% discount on all our collections, so you can always stay up to date! * Flexible compensation package with tax advantages: medical insurance, training, catering, and childcare program. * Free company transportation from Barcelona and El Vallés. * At Mango, we invest in your personal and professional growth. Access a wide range of training opportunities, personalized mentorships, continuous development programs, and internal promotion opportunities that will drive you toward success. Technically, you will have the chance to train on various technological platforms, as well as participate in workshops, meetups, practice communities, team buildings, and company meetings. * Think big! Mango offers international opportunities in over 120 markets to expand your horizons and grow with us globally. At Mango, we believe in an inclusive culture where creativity and innovation inspire us to take fashion further. Therefore, we are committed to providing equal opportunities for everyone, valuing the authenticity of each individual. Taking Fashion Further
Carrer del Camí Reial, 49, 08184 Palau-solità i Plegamans, Barcelona, Spain
Senior Group Director Scientist63839249390977123
Indeed
Senior Group Director Scientist
The Senior Group Director Scientist fulfills the role of line manager to a number of clinical scientists within Hematology Research and Development. The role will have a major responsibility to mentor junior clinical scientist within Hematology. The role holder may be required to serve as a member of the departmental leadership team, coordinate assets tracking and lead improvement initiatives in service of non\-drug scorecard objectives. You will also fulfill the role of a Senior Clinical Scientist assigned to Hematology and in that capacity you are an important part of the project Team, working collaboratively with the program and study level physician or clinical lead as their guide in medical scientific aspects of the compound and its development. The accountabilities are broad however, the core accountabilities are the medical \& scientific support for the development and implementation of early phase AstraZeneca sponsored clinical program strategy, externally sponsored collaborative research program strategy and studies, including clinical science support for initiating clinical trial(s), protocol/amendment development, IB/DSUR submissions, clinical trial documents, supporting clinical data review, interpretation of the study results and providing/supporting final recommendations to senior management. You will drive and provide guide input to other non\-assigned programmes, process improvement initiatives, development of junior clinical scientist within Hematology and provides strategic contributions to the global clinical scientist team. As a key leadership member of the Global Project Team, this position demands strong collaborative communication skills, including the ability to engage with and influence a diverse range of business partners both within and external to AstraZeneca. * Will be required to line lead other Clinical Scientists including project allocations/resource management, recruitment \& selection, personal development and performance management * May be required to serve as the Skills Lead for the Clinical Science group thereby being responsible for ensuring appropriate procedures, training and personal development approaches are in place for the skill group and standard methodology is identified and implemented * Contributes to the Departmental Leadership Team to ensure effective ways of working, identification and resolution of issues, departmental objective setting and may extend to prioritization and supervising at the departmental level * Will lead or contribute to continuous improvement initiatives * May be required to run key alliances (provider and academic) • As required you may be asked to act as Clinical Lead for the program/study or support the clinical lead • Leads or supports clinical input to the clinical development plan at all stages of the programme. * Leads or co\-lead (with Translational and Bioscience Leads) the science\-to\-man sub team (TSST) to integrate the biology, translational and clinical science into the programme strategy * Leads/supports development of recommendation(s) on further development strategies to internal committees. * Leads (or supports, as required) the preparation of clinical and other data for governance and other presentations * Provide scientific/medical mentorship to the study team, including the CRO team. * Is responsible for the collaboration with the research scientists and translational scientists to provide clinical input to the development and review of data to support development of the pre\-CDID compounds * Follows important developments and trends in the medical \& scientific literature and disseminates updates to the project team and beyond ensuring all involved parties are aware of key developments and the impact on the strategy * Leads the development and review of content and quality of publications and inputs to development of the publication strategy * Where required leads project specific reviews of the competitor landscape to advise the program strategy * As required, the Group Director Clinical Scientist may be asked to act as Clinical Lead for the AZ sponsored study * Guides aspects of the Clinical Development Plan (CDP) and Clinical Study Protocols in keeping with the approved CDP and ensuring linkage of trial data to target product profile * Attends (in person or by TC) the Site Initiation Visits, to present the study design and key aspects of the protocol * Leads, (or supports as required), clinical data review and interpretation of the study and program level with input from the study or program Physician/Clinical Lead * Owns the compilation and interpretation of the data for and from the dose escalation committee/safety review committee, in collaboration with the program physician * Leads, approves or provides input for the protocols, amendments, Investigator Brochure, DSURs and other relevant strategic documents. Acts as lead clinical reviewer for Clinical Study Reports * Develops and builds investigator and site relationships to support site selection and study start up activities * Leads the development and implementation of the externally sponsored collaborative research (ESCR) strategy for a programme. The clinical scientist is the link between the project team and all external clinical research for the programme. For preclinical external research proposals, co\-leads with the Bioscience Lead. * Leads investigator/site relationships for ESCR clinical proposal reviews, protocol review and approval, scientific oversight and discussions for academic basket/umbrella and ESCR studies • Represents the project internally and supports oncology drug development externally as a medical scientific guide with key external collaborators. Supports development of alliances as appropriate. * Support due diligence activities for potential in\-licensing or collaborative opportunities and provides recommendations to senior management * Represents AstraZeneca as a support for external meetings such as advisory boards and • Identifies and handles risks within the ESCR portfolio, raises quality issues through the appropriate channels, maintains communications with key AstraZeneca partners as required. * Drives key critical initiatives within and beyond the Early Clinical Oncology group • Develops, coaches, mentors, motivates and encourages individuals within the organisation * Operates in compliance with GCP and relevant regulatory guidelines. **Essential Requirements:** * PhD or Pharm D with at least 10 years experience in the industry * Strong Experience working on clinical trials in Hematology \-Oncology clinical trials experience required. * Experience handling and interpreting the results of clinical trials as well as exposure to writing protocols * Strong analytical skills * Experience of authoring scientific documents * Well\-developed communication skills * Sufficient technical and disease area knowledge to be able to interact with confidence with internal and external partner * Proven track record of line management
Carrer de Joan Güell, 114, Les Corts, 08028 Barcelona, Spain
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