In addition to the responsibilities listed above, the Therapeutic Strategy VP will be expected to: Lead and support clinical trial design and all associated aspects for various clients. Provide strategic and therapeutic area guidance for clinical development plans in compliance with applicable regulatory, medical, and ethics guidelines.
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.
Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. Design and implement a SQL-based landing zone for regulatory data Develop stored procedures for transformation, enrichment, and aggregation Build and operate high-volume batch processing chains for monthly/quarterly cycles Implement SSIS-based ingestion flows and job orchestration Ensure data quality, technical lineage, and full traceability across layers Define and document integration patterns and mapping logic between landing-zone datasets and Tagetik-based reporting templates Perform operational monitoring, troubleshooting, and performance optimization Strong expertise in Microsoft SQL Server and T-SQL Hands-on experience with stored-procedure-driven ETL and complex data models Solid SSIS skills for orchestration and control of processing chains Experience with batch processing, logging, restartability, and performance tuning Knowledge of data lineage, reconciliation, and regulatory processing needs Experience with reporting platforms such as Tagetik is a plus Familiarity with Oracle source systems is advantageous Renowned Client Remote Option Ihr Kontakt Ansprechpartner Eliška Stejskalová Referenznummer 862801/1 Kontakt aufnehmen E-Mail: eliska.stejskalova@hays.at Anstellungsart Freiberuflich für ein Projekt
Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. Design and implement a SQL-based landing zone for regulatory dataDevelop stored procedures for transformation, enrichment, and aggregationBuild and operate high-volume batch processing chains for monthly/quarterly cyclesImplement SSIS-based ingestion flows and job orchestrationEnsure data quality, technical lineage, and full traceability across layersDefine and document integration patterns and mapping logic between landing-zone datasets and Tagetik-based reporting templatesPerform operational monitoring, troubleshooting, and performance optimization Strong expertise in Microsoft SQL Server and T-SQLHands-on experience with stored-procedure-driven ETL and complex data modelsSolid SSIS skills for orchestration and control of processing chainsExperience with batch processing, logging, restartability, and performance tuningKnowledge of data lineage, reconciliation, and regulatory processing needsExperience with reporting platforms such as Tagetik is a plusFamiliarity with Oracle source systems is advantageous Renowned ClientRemote Option Ihr Kontakt Ansprechpartner Eliška Stejskalová Referenznummer 862801/1 Kontakt aufnehmen E-Mail: eliska.stejskalova@hays.at Anstellungsart Freiberuflich für ein Projekt
This role requires a highly experienced biostatistician capable of working independently, representing the Biostatistics function within cross‑functional teams, and delivering high‑quality statistical input throughout study design, execution, and analysis. Key Responsibilities Statistical Leadership & Study Support Serve as the primary statistical lead and main point of contact on the Clinical Trial Team (CTT), representing Biostatistics with confidence and professionalism.Work independently to support clinical teams, providing proactive statistical guidance throughout the study lifecycle.Lead statistical strategy discussions, including endpoint definitions, analysis methods, risk mitigation, and regulatory expectations.
We bring together sector expertise, global scale and local knowledge to design and manage supply chains from raw materials and manufacturing through to the delivery of finished goods and return services. And by seamlessly connecting local operations across the world we are able to deliver the future of global trade.
Deine Aufgaben: Technische Betreuung und kontinuierliche Weiterentwicklung unseres bestehenden ProduktportfoliosEntwicklung und konstruktive Umsetzung von Produktoptimierungen mit Fokus auf Qualität, Funktionalität und HerstellbarkeitKonstruktion von Bauteilen und Baugruppen mittels 3D-CAD-SystemenErstellung und Pflege technischer Zeichnungen sowie KonstruktionsunterlagenPlanung, Definition und Begleitung von Verifikations- und ValidierungstestsTechnische Bewertung und Umsetzung von Design- und Änderungsanträgen im Rahmen des Change-Management-ProzessesAnalyse technischer Fragestellungen und Reklamationen in Zusammenarbeit mit Testing & AnalysisSicherstellung konsistenter Produktdaten durch Pflege von Stücklisten, Änderungsständen und technischen Stammdaten im ERP-System (SAP)Enge bereichsübergreifende Abstimmung mit Qualitätsmanagement, Regulatory Affairs, Produktion, Supply Chain sowie externen Partnern Dein Profil: Abgeschlossenes Studium im Bereich Maschinenbau oder vergleichbare technische QualifikationMehrjährige Erfahrung in Konstruktion, Produktpflege oder Entwicklung, idealerweise im regulierten Umfeld (z.
Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
Design Verification & Entwicklung Planung, Durchführung und Koordinierung von Design-Verifizierungen für Produkte in der EntwicklungErstellung von Verifizierungsplänen, Prüfstrategien und einreichungsrelevanten BerichtenEigenständige Durchführung von Design-Verifizierungsstudien????
Responsible for the inclusion of Cardiovascular elements into proposals.Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy.
Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
Your assignments Producing designs, both initial outlines and full plans, of sewerage, water treatment and flood defence structures such as pump systems and pipe networksPresenting project details and technical information to colleagues and clientsWriting reportsManaging project budgetsKeeping up to date with changes in regulatory legislation and guidelinesWriting and advertising tender documents and managing contractsLiaising with clients, contractors, government agencies, local authorities and suppliersSupervising local staff and site workersUsing a variety of specialist computer applications/simulation softwareMaintain effective relationships with members of all divisions and departments responsible for performing services related to the projectPrepare construction cost estimates, perform construction monitoring and coordinate field activities Your profile University degree (M.Sc.) in civil engineer, mechanical engineer, process or environmental engineer or other suitable qualification Experience in the preparation of master plans, feasibility studies, tender documents and construction planning, and/or experience with construction supervision, project management and/or commissioning of water supply and/or wastewater treatment facilities.Preferably 5 years of professional experience in international consulting/engineering in the field of urban water management, preferably in projects financed by bilateral and multilateral donor organisations and development banksStructured approach to work a high degree of flexibility, initiative, persuasiveness and negotiation skills as well as the ability to work in a team Willingness to travel extensively Good knowledge of written and spoken English and preferably an additional business language (French, Spanish, etc.)
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.
You develop concepts and participate in feasibility studies to meet technical requirements You perform and take ownership of specific software development tasks, ensuring reviews using checklists and templates You lead work package definition, estimation, and planning, and enhance or document SW unit specifications and designs You review designs and contribute to the SW architecture, defining quality attributes and staying updated with technology trends You conduct root-cause analysis of complex issues and provide bug fixes for post-market software releases You ensure compliance with processes, propose improvements, and stay informed about regulatory and market standards Education in a software related field such as software or electrical engineering Industry experience Proven experience as a Software Engineer with a strong focus on Rust development Solid understanding of Rust's core concepts, including ownership, borrowing, and lifetimes Experience with asynchronous programming in Rust (e.g., using async/await) Familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx) Experience with Linux and Dockers Internal career opportunities World renowned pharmaceutical company International and diverse environment Ihr Kontakt Referenznummer 865359/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Du erarbeitest mit uns einen Entwicklungsplan und übernimmst dessen Management, um mit uns einen Innovationsvorsprung aufzubauen.Du baust mit uns ein Team aus talenterten Ingenieuren auf, die bei Design und Entwicklung der Elektroden und Chips unterstützen.Du unterstützt anschließend den weiteren Aufbau des Unternehmens: du etablierst und leistest Quality-, Regulatory- oder Clinical‑Trial‑Funktionen oder entwickelst Market‑Access‑ und Vertriebsstrukturen und sicherst die erfolgreiche Markteinführung unseres BCIs.Du koordinierst die Schnittstellen zu unseren Entwicklungspartnern und internen FUTRUE-Teams und steuerst Timeline und Budget der Entwicklung.
You develop concepts and participate in feasibility studies to meet technical requirementsYou perform and take ownership of specific software development tasks, ensuring reviews using checklists and templatesYou lead work package definition, estimation, and planning, and enhance or document SW unit specifications and designsYou review designs and contribute to the SW architecture, defining quality attributes and staying updated with technology trendsYou conduct root-cause analysis of complex issues and provide bug fixes for post-market software releasesYou ensure compliance with processes, propose improvements, and stay informed about regulatory and market standards Education in a software related field such as software or electrical engineering Industry experienceProven experience as a Software Engineer with a strong focus on Rust developmentSolid understanding of Rust's core concepts, including ownership, borrowing, and lifetimesExperience with asynchronous programming in Rust (e.g., using async/await)Familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx) Experience with Linux and Dockers Internal career opportunities World renowned pharmaceutical companyInternational and diverse environment Ihr Kontakt Referenznummer 865359/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Dein Fokus liegt dabei auf drei wesentlichen Aufgabenbereichen: Technologieentwicklung: Designe mit uns die neue Generation an Brain-Computer-Interfaces. Leiste einen entscheidenden Beitrag in der Entwicklung von Probe & Electrode, sowie Chip & Connectivity.
</li> </ul> Cross-Functional Collaboration <ul> <li>Work closely with Electrical Design Engineers, Systems Engineers, Manufacturing, Installation, and Quality teams.</li> <li>Support production, installation, and maintenance troubleshooting related to wiring documentation.
You will collaborate closely with the commercial department and other departments e.g. global sales, product design and scientific affairs. International travel to visit customers and colleagues is expected in the amount of 20-30 days per year. The position is based at Chr.
You will collaborate closely with the commercial department and other departments e.g. global sales, product design and scientific affairs. International travel to visit customers and colleagues is expected in the amount of 20-30 days per year. The position is based at Chr.
Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. Design, build and optimize enterprise Tableau dashboards Develop reporting-friendly data models on Cloudera Data Platform (Hadoop) and Azure Databricks (Delta Lake, SQL Warehouses) Implement and tune SQL queries (Hive, Impala, Spark SQL, Databricks SQL) for performance, cost efficiency and concurrency Apply Tableau performance optimization strategies (extract vs live, push-down optimization, query tuning) Design and implement secure enterprise Tableau configurations, including row-level security aligned with role concepts Ensure compliance with IT security, data governance and regulatory requirements Collaborate with data platform teams, DataOps, IT security/compliance and controlling solutions Produce professional documentation: data models, dashboard specifications, data-source definitions, security concepts, test cases Conduct testing for accuracy, performance, access control and stability of dashboards and data models Provide knowledge transfer, coaching and structured handover to internal teams Strong hands-on experience with Tableau Desktop and Tableau Server/Cloud in enterprise environments Proven ability to build management-ready dashboards for finance/controlling or other regulated industries Practical experience with Cloudera Data Platform, Hadoop ecosystems, and Azure Databricks integrations Advanced SQL skills across Hive, Impala, Spark SQL, Databricks SQL Solid understanding of Delta Lake, parquet/ORC formats, and BI-oriented data modeling principles Experience implementing row-level security and with enterprise BI solutions Strong knowledge of performance optimization in Tableau, Hadoop and Databricks environments Ability to operate in regulated financial environments with security, compliance and data governance constraints Excellent communication and documentation skills in English International client Remote option Ihr Kontakt Ansprechpartner Eliška Stejskalová Referenznummer 864486/1 Kontakt aufnehmen E-Mail: eliska.stejskalova@hays.at Anstellungsart Freiberuflich für ein Projekt
Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. Design, build and optimize enterprise Tableau dashboardsDevelop reporting-friendly data models on Cloudera Data Platform (Hadoop) and Azure Databricks (Delta Lake, SQL Warehouses)Implement and tune SQL queries (Hive, Impala, Spark SQL, Databricks SQL) for performance, cost efficiency and concurrencyApply Tableau performance optimization strategies (extract vs live, push-down optimization, query tuning)Design and implement secure enterprise Tableau configurations, including row-level security aligned with role conceptsEnsure compliance with IT security, data governance and regulatory requirementsCollaborate with data platform teams, DataOps, IT security/compliance and controlling solutionsProduce professional documentation: data models, dashboard specifications, data-source definitions, security concepts, test casesConduct testing for accuracy, performance, access control and stability of dashboards and data modelsProvide knowledge transfer, coaching and structured handover to internal teams Strong hands-on experience with Tableau Desktop and Tableau Server/Cloud in enterprise environmentsProven ability to build management-ready dashboards for finance/controlling or other regulated industriesPractical experience with Cloudera Data Platform, Hadoop ecosystems, and Azure Databricks integrationsAdvanced SQL skills across Hive, Impala, Spark SQL, Databricks SQLSolid understanding of Delta Lake, parquet/ORC formats, and BI-oriented data modeling principlesExperience implementing row-level security and with enterprise BI solutionsStrong knowledge of performance optimization in Tableau, Hadoop and Databricks environmentsAbility to operate in regulated financial environments with security, compliance and data governance constraintsExcellent communication and documentation skills in English International clientRemote option Ihr Kontakt Ansprechpartner Eliška Stejskalová Referenznummer 864486/1 Kontakt aufnehmen E-Mail: eliska.stejskalova@hays.at Anstellungsart Freiberuflich für ein Projekt
Skills and Abilities: Ability to identify additional service/system requirements or shortfalls and co-ordinate and/or design the delivery of innovative solutions to maximise service quality, efficiency and continuity. Ability to ensure professional and quality service standards are maintained and applied within own area of activity.
Clinical and market insight: Collect product performance and user feedback for R&D, MACA, and commercial teams to inform life cycle management, next-generation innovations, clinical study designs, and commercial strategies. Share insights, best practice, and data with national and regional MSL networks. Cross-functional collaboration and influence: Partner with internal cross-functional teams, including MACA, R&D, Regulatory, Marketing and national Market Access, to ensure integration of insights into our strategies.
As part of our team, you will take on the following responsibilities: You are responsible for the implementation, administration, monitoring, and maintenance of IT systems and services in a Windows Server environment, in compliance with defined security policies.You analyze and resolve incidents in 2nd- and 3rd-level support within the Windows Server infrastructure.You implement hardening measures to reliably meet regulatory, compliance, and security requirements.In addition, you ensure the continuous development of the systems, with a focus on security, efficiency, and stability, and guarantee stable operations as well as correct and efficient licensing within lifecycle management.You manage and monitor external service providers and ensure a high level of service quality.You conduct market analyses for the selection and evaluation of hardware and software products.You design and implement concepts for server and application operations in compliance with defined security policies.You plan, coordinate, and support IT projects and business sub-projects from realization through testing to rollout.You advise business departments on projects, changes, and adjustments to IT services, systems, and applications.You analyze and evaluate functional, technical, and business requirements and ensure their secure integration.You identify potential for process optimization, automation, and interface improvements and implement them sustainably.
As a Compliance Engineer, you will be responsible for providing the Design, Production, Test, and Service departments with up-to-date guidance and support to ensure that our products comply with the latest relevant legislation.
The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to the Clinical Trial Report (CTR) and serves as a core member of both the Trial Team and the Evidence Network Team.
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectives Design and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regions Build and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutions Conduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiatives Contribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical data Oversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL Director Act as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentation Plan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical Officer Represent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencers Serve as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic community Collaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groups Full professional proficiency in English, both spoken and written Strong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflows Experience with product launches, advisory boards, and post-approval studies is highly advantageous Relevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned company Other Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Your Role In this position, you will: • Support the implementation and regional rollout of global compliance and internal control strategies in close collaboration with the Head of ICS • Monitor and review internal control systems, identifying risks, gaps, and opportunities for improvement • Document, analyze, and report compliance activities, findings, and follow-up actions to relevant stakeholders • Provide guidance and hands-on support to regional teams on compliance policies and internal control requirements • Design and deliver training initiatives to increase awareness and understanding of internal controls and compliance topics • Contribute to regional risk assessments by identifying, prioritizing, and helping mitigate key risks • Collaborate with other regional managers to share best practices and ensure consistency across regions • Monitor regulatory developments at local level and assess their impact on internal control and compliance practices • Work closely with internal audit teams and contribute to broader internal initiatives as needed Your Profile Must-haves • Bachelor’s degree in Business Administration, Finance, Law, or a related field • Several years of professional experience (typically 5+ years) in internal controls, compliance, risk management, controlling, or a comparable function • Solid knowledge of internal control systems and compliance frameworks • Strong analytical skills with high attention to detail • Knowledge of SAP FICO and/or other ERP systems • Clear and confident communication skills, with the ability to engage effectively across different organizational levels • Fluency in English (written and spoken) • Willingness to travel internationally (approximately 40%) Nice-to-haves • Experience working in an international environment, ideally within a listed company • Experience with compliance, audit management, or data analytics tools • Additional language skills such as German or another European language What Makes You a Great Fit You bring a strong sense of integrity and accountability to everything you do and are motivated by delivering high-quality, reliable outcomes.
Experience in set-up and conduct of Phase II clinical trials including in depth knowledge of early phase study designs, protocol writing and clinical pharmacology. Additional experience in conduct of Phase I and Phase III trials would be an advantage.
You would also: Act as a key member of the Legal & Compliance function, supporting in the development, implementation and ongoing oversight of the Group’s compliance programs including anti-corruption, anti-trust and export control/trade sanctions and help identify, manage and solve compliance risks, and advise on compliance topics. Design, develop, and continuously improve the EMEIA Division’s compliance programs and keep abreast of relevant regulatory developments across the EMEIA Division, raise awareness and adoption of compliance programs through regular compliance training.
Your Contribution Identify high-value market segments; analyze MedTech trends (FDA, CE, emerging technologies); develop multi-year account strategies aligned with the SBF's commercial roadmap.Own full lifecycle of opportunities; maintain 3× pipeline coverage; provide CRM-based forecasting with ±10% accuracy; ensure pursuit discipline and qualification rigor.Lead complex, cross-functional projects across Engineering, Operations, Quality, Regulatory, and Finance to advance design, feasibility studies, new business development initiatives, and portfolio optimization.Establish and strengthen relationships with executive-level decision makers (CTO, CIO, Program Directors, Supply Chain); Serve as the primary commercial interface for strategic accounts.Shape value propositions, pricing strategies, and competitive positioning; build ROI-based business cases; support margin expansion and commercial improvement initiatives.Build territory and account plans; deliver accurate monthly and quarterly forecasts; track performance KPIs and implement corrective actions.Drive CRM discipline, BD process standardization, and continuous improvement; enhance tools, governance, and business development workflows.Foster strong internal alignment across Sales, Marketing, Engineering, Operations, and Quality.Represent SCHOTT at key industry conferences; Contribute to thought-leadership, marketing collateral, and campaign strategy.
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.
As part of our team, you will take on the following responsibilities: You are responsible for the operation, continuous development, and hardening of our enterprise‑wide PKI landscape (on‑premises and cloud).You design, implement, and operate Azure‑based PKI services, in particular Microsoft Cloud PKI and Microsoft Intune Certificate Lifecycle Management.You integrate certificate services into modern zero‑trust architectures.You develop and implement secure certificate and key management processes.You support the modernization of our identity and security infrastructure, especially in hybrid Azure environments.You work closely with security and infrastructure teams to establish secure and automated certificate workflows.You actively contribute to IT security projects and create security and architecture concepts.In close collaboration with the Group Information Security Office, you ensure compliance with regulatory and internal security requirements.You drive continuous process optimization, automation, and documentation.
What makes you stand out You hold a master’s degree in Computer Science, Software Engineering, Mathematics, Statistics, or a related quantitative field.You have at least 3 years of professional experience in ML Engineering or MLOps, with a proven track record of building, deploying, and operating tailored AI/ML solutions in production.You bring deep expertise in Python and SQL, hands‑on experience with cloud platforms (ideally Azure), and familiarity with data warehouses such as Snowflake; foundational knowledge of Infrastructure‑as‑Code tools like Terraform is a plus.You are proficient with CI/CD tools (e.g., Azure DevOps), containerization technologies (Docker/Kubernetes), and apply modern software design patterns confidently.You thrive in a dynamic, agile, and innovative environment, working effectively both independently and as part of a team.You possess excellent English communication skills, both written and spoken; German language skills are considered a plus.
As part of our team, you will take on the following responsibilities: As an Infrastructure Architect (gn), you analyze the existing system and infrastructure landscape and, based on this, develop technical design changes for new software and hardware solutions. You design, plan, and implement infrastructure technology solutions and ensure their sustainable integration into the existing architecture.You are responsible for managing and continuously developing the existing IT services and contribute your expertise in an advisory capacity to other internal IT units.