Brand Manager Digital (m/f/x) Location: Munich Contract: Full-time / Permanent Reporting to: Head of Marketing The Opportunity As a Brand Manager Digital, you will play a pivotal role in shaping the success of our flu and travel vaccine portfolio. You will design and execute data‑driven, multi‑channel marketing strategies that deliver relevant, high‑quality content to healthcare professionals and key stakeholders.
Your Profile Bachelor's degree in Engineering, Physics, Materials Science, or related technical discipline; Master's degree preferred.7+ years of experience in application engineering, product engineering, or technical customer support for medical, optical, or high-reliability components.10+ years of experience supporting medical device OEMs or optical/photonics customers preferred.Strong experience with customer interaction, specification management, and technical communication.Ability to interpret drawings, tolerances, and material/process requirements; hands-on lab and testing experience preferred.Experience with cross-functional collaboration (Sales, Engineering, Product Management, Quality, Operations).Excellent written/verbal communication, presentation skills, and problem-solving capability.Experience supporting verification, validation, and application testing preferred.Some familiarity with medical product standards, regulatory documentation expectations, and design control practices.Experience with DOE, statistical tools, and structured problem-solving (e.g., 8D) preferred.Experience in global, matrixed organizations preferred.Must be able to read, write, and speak EnglishEffective verbal and written communication skills.Self-motivated and results oriented.Due to the nature of work performed at this facility, US Person status may be required.
Work location: Germany (on-site rotation system) The Concrete Towers business unit is dedicated to the design, manufacturing, and installation of concrete towers for wind turbines. As a Quality Technician SITE (m/f/d), you will play a key role in ensuring quality standards during the construction and installation of concrete towers.
Vorbereitung und Erstellung regelmäßiger (monatlicher) Baufortschrittsberichte. Organisation und Protokollierung aller Arten von Projekt-, Design- und Bau-Meetings. Verantwortung für die Projektdokumentation und Übergabe beim Projektabschluss. Du wirst systematisch an mehreren Projekten gleichzeitig unter der Aufsicht eines erfahrenen Projektmanagers und in Zusammenarbeit mit verschiedenen Teammitgliedern - auch aus anderen Geschäftsbereichen - arbeiten.
Work location: Germany (on-site rotation system) The Concrete Towers business unit is dedicated to the design, manufacturing, and installation of concrete towers for wind turbines. As a Quality Technician SITE (m/f/d) , you will play a key role in ensuring quality standards during the construction and installation of concrete towers.
Work location: Germany (on-site rotation system) Concrete Tower's business unit is dedicated to the design, manufacturing, and installation of concrete towers for wind turbines. As a BoP Civil Site Supervisor (m/f/d), you will play a key role in supervising civil works and ensuring compliance with safety and quality standards.
Work location: Germany (on-site rotation system) Concrete Tower's business unit is dedicated to the design, manufacturing, and installation of concrete towers for wind turbines. As a BoP Civil Site Supervisor (m/f/d) , you will play a key role in supervising civil works and ensuring compliance with safety and quality standards.
Key Responsibilities: Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company Represent sponsors at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee Participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication Participate as high level lead biostatistician on major projects, including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or NDA sections Leading studies at an operational level Provide expert review and initiate methodology development work with regards to statistical standards and validation procedures Consult on operational/statistical/therapeutic area topics Knowledge Sharing: Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses Performs as subject matter expert (SME) Risk Management: Identifies risks to project delivery and/or quality, leads in a way to minimize risks Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions Lock and Unblinding Process: Leads the database lock and unblinding process for the statistical team Participate on the biostatistics randomization team (drafts randomization specifications and/or perform quality control (QC) review of randomization schedules) Statistical Expertise: Provide expert statistical input into review of statistical deliverables (i.e. statistical section of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures, and statistical sections for complex and/or integrated reports) Provide expert input into data management deliverables (i.e. database design, CRF design, validation checks and critical data) Provide expert review of ADaM reviewers guide (ADRG) and metadata Perform senior biostatistical review (SBR) Produce or perform quality control review of sample size calculations for complex studies Requirements: Masters or PhD degree in Biostatistics or a related field with relevant experience within the life-science industry Expert in a broad range of complex statistical methods that apply to Phase 2-3 clinical trials Expert in strategically collaborating with clinical and drug development expertsExperience in serving as statistical lead for regulatory submissions, including preparation of submission datasets, eCTD support, meeting with regulatory teams, and responding to regulatory queries In-depth knowledge of applicable clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Strong working knowledge of SAS or RExcellent knowledge of CDISC Data Standards Superb communication and collaboration skills Independent and pro-active problem solving skills IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Key Responsibilities Design and delivery of mechanical designs using 3D CAD. Documentation of designs, their prototyping and validation, facilitating design reviews, and delivery through Operations into customers.
Exceptional problem-solving and algorithmic thinking skills, coupled with a deep understanding of software design patterns and clean code principles. Expert-level knowledge and practical experience in building modern, scalable web applications using React, TypeScript, and advanced CSS/Styling techniques.
Exceptional problem-solving and algorithmic thinking skills, coupled with a deep understanding of software design patterns and clean code principles. Expert-level knowledge and practical experience in building modern, scalable web applications using React, TypeScript, and advanced CSS/Styling techniques.
Company description 💧 Aliaxis is a leading technology company that designs sustainable, easy to install, and innovative fluid management solutions. Over 15,000 people have selected to work for us in more than 40 countries, meeting our customers’ most demanding needs for pipes and fitting systems in building, infrastructure, industrial and agriculture sectors.