Education/Certification Required Bachelor’s Degree About the Opportunity Position Summary Reporting to the Vice President of Sales and Marketing, the Business Development Manager is responsible for delivering new customers from their network in Supply Chains, FMCG, Retail, Automotive, 3PL, Pharma and Chemical.
Strong Experience in Monitoring and Observability of the infrastructure (Datadog preferred) and vulnerabilities discovery and tracking with tools such us Falco, Guardduty Strong experience in architectural design for cloud optimized applications Fluent in English both spoken and written Nice to have: AWS or K8s certifications Additional information: **Working model: Due to the upcoming tasks and responsibilities for this position, it is required to work onsite at our headquarters in Hamburg or Berlin on a weekly basis. Therefore we’ve implemented a hybrid working model that allows us to work remotely on Mondays and Fridays and to work onsite from Tuesday to Thursday.
This position will be responsible for setting and achieving sales targets and contributing positive financial results to the overall North American business.
Sollten wir danach gemeinsam zum Ergebnis gelangen, dass diese Position gut zu Ihren beruflichen Zielen passt, werden wir Sie bei unserem Mandanten (nach erneutem Einverständnis ihrerseits) vorstellen.
Work Authorization: DHL Global Forwarding will only employ those who are legally authorized to work in the United States. This is not a position for which visa sponsorship will be provided. Individuals who need sponsorship for work authorization, now or in the future, are not eligible for hire for this role.
JOIN OUR TEAM IN COLOGNE FOR A FULL-TIME POSITION, STARTING AS SOON AS POSSIBLE. Senior Expert “Automation Designer (m/f/x)” in the Center of Digitization DO YOU HAVE PLENTY OF KNOWLEDGE AND WANT TO MAKE A DIFFERENCE?
Severely disabled applicants will be given preference if equally qualified. This position can be full-time or part-time (min. 30h/week). DKV Mobility is looking for the best talents and knows that these are not always available on a full-time basis.
Gemeinsam treiben wir den digitalen Wandel in der Automobilbranche voran. Ihr Ansprechpartner für diese Position ist Herr Jan Hagen (Personalreferent). 0441-21020228 LinkedIn Jan Hagen Ihr Interesse wird von uns selbstverständlich absolut vertraulich behandelt.
To learn more please visit http://www.convatecgroup.com Position Overview The Medical Scientific Liaison is a key position within our Medical Affairs function, primarily supporting Convatec’s nitric oxide next-generation antimicrobial platform (CNAP) business.
Work Authorization: DHL Global Forwarding will only employ those who are legally authorized to work in the United States. This is not a position for which visa sponsorship will be provided. Individuals who need sponsorship for work authorization, now or in the future, are not eligible for hire for this role.
#Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #Compensation: Commitment deserves reward – overtime or multi-day assignments are additionally compensated.
If you are an experienced pharmaceutical product development strategist looking for a challenging and rewarding role, we encourage you to apply for this position. Preference will be given to candidates with recent previous health authority experience (current or EU/EMA medical reviewers, etc.)
Identify and assess new product opportunities, development projects and business fields with a strong emphasis on gynecology/women’s healthLead negotiations for licensing agreements and development partnerships, including coordination of contract draftingManage cross-functional projects, ensuring alignment of commercial and pharmaceutical requirementsConduct and support patent research, including preparation of risk assessments for upcoming market launchesCollaborate closely with international sales affiliates and internal portfolio stakeholdersRepresent the company at national and international conferences, trade fairs and industry events A completed degree in pharmacy, business administration or a related fieldRelevant experience in Business Development within the pharmaceutical industry, with a clear focus on gynecology or women’s health portfolioStrong communication skills, a collaborative mindset and the ability to work with diverse stakeholdersA proactive, solution-oriented approach with strong resilience in negotiation settingsBusiness-fluent in English, additional languages are an advantageWillingness to travel up to approx. 25% A secure and long-term position within a stable and expanding pharmaceutical organisationFlexible hybrid arrangement, allowing remote workA competitive compensation package incl. additional financial benefitsHybrid working options Extensive opportunities for professional and personal development Gehaltsinformationen An attractive remuneration package awaits you Ihr Kontakt Ansprechpartner Kristine Klein Referenznummer 858726/1 Kontakt aufnehmen E-Mail: kristine.klein@hays.de Anstellungsart Festanstellung durch unseren Kunden
Register now and look forward to many interesting and suitable positions and projects. Support of GSR ISA homologation activities focus on Intelligent Speed Limit Assist Development of test processes/procedures including measurement tools Real vehicle tests of Drivers Assistance Systems with appropriate validation toolsPlanning, coordination and preparation of test vehicles ADAS sign-off tests of EU vehicles Support and execution of proving-ground tests Support and drive development work at tier-1 level Analysis of test data, identification of improvement potentialAnalysis of competitor vehicles and definition of future sensor strategies Degree in Electrical, Mechanical, Mechatronic Engineering or similarExperience in similar position at tier-1 or OEM and in specification/development and validation of ADAS Systems Experience with validation tools (DGPS, datalogging, etc.)Ability to develop and set up standard test procedures and processes Experience to support and drive development work at tier-1 level would be a plus Familiar with ADAS system hard- and software architecture Willingness to work in intercultural teams and good command of English language 30 days leave per yearA highly motivated team and an open way of communication A very renowned companyDynamic and innovative market environment Ihr Kontakt Ansprechpartner Annika Chrysant Referenznummer 863151/1 Kontakt aufnehmen E-Mail: annika.chrysant@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Additional experience in BIM and technical software would be desirable We offer Permanent Position Flexible working environment (mobile office/office hours)Friendly and collaborative spirit in multidisciplinary teamsHigh degree of personal responsibilityFinancial benefits (e.g. participation in corporate success)Challenging projects, where you can develop both professionally and personallyMultiple internal and external training opportunitiesCanteen nearby (meal allowance)Office amenities (e.g. company sports, free water, coffee and tea) Please send your application to Christina Müller When applying for a job at GKW Consult, please note our information on data protection for applicants.
You properly manage costs, investments and all factors affecting a profitable performance You report on sales, business performance, market information and finance YOUR PROFILE You have management and commercial experience in the food ingredients industry You demonstrate strong leadership with expertise in building high performing teams You have strong analytical skills and financial knowledge You have a commercial or food technology bachelor or master’s degree You are a native German speaker and you have fluent English language skills This position offers a key role within a growing, non-bureaucratic company environment which values entrepreneurship. YOUR CONTACT Our consultant Sandra Haindl (+49 89 1895520-18) will be happy to provide you with additional information.
Create your future by joining our Graduate Trainee Program where you will have the opportunity to work on a full-time contract position for 18-months. Upon successful completion of the program, you stand a chance to be shortlisted for exciting job opportunities based on your career aspirations, your performance and also on business needs and available vacancies.
Maintain and troubleshoot data integration pipelines to ensure stable data flow into AI and analytics systems Support model development by assisting with training, validation, and optimization of machine learning workflows Conduct data analysis to extract insights and provide clear reports supporting R&D research questions Solve technical challenges related to data access, pipeline performance, and software limitations Ensure continuity of ongoing projects by aligning closely with the core team and delivering on timelines Perform image analysis and prepare datasets required for scientific and ML use cases Manage and improve ETL processes to ensure data quality, structure, and availability Document workflows, pipeline changes, and analytical steps to ensure clarity and reproducibility Academic background in computer science, data science, engineering, or a related quantitative field Strong proficiency in Python with expertise in scientific and analytical libraries Skilled in SQL and working with relational databases Understanding of ETL concepts and practical experience working with data pipelines Solid foundation in machine learning principles and model lifecycle Ability to perform image analysis for scientific or research applications Strong communication and interpersonal skills with the ability to collaborate in a technical team Independent, structured problem-solver with a commitment to clear documentation and FAIR data practices Opportunity to contribute directly to active R&D projects with immediate real-world impact Hands-on involvement in AI, machine learning, and data integration challenges in a scientific environment Close collaboration with a small, highly skilled technical team Ihr Kontakt Referenznummer 863771/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
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
Own, author, record and investigate Deviations across operationsCollaborate with Subject Matter Experts and key stakeholders to determine root causes and assess product or system impactApply structured investigational tools such as Fault Tree Analysis, Event & Causal Factors Chart, Fishbone Diagram and similar methodologiesDefine effective CAPAs and associated effectiveness checks to prevent recurrenceEnsure full cGMP compliance throughout the investigation lifecycleDrive quality records to timely and accurate completionSupport continuous improvement activities within operationsContribute to enhancing investigation quality, consistency and efficiencyMaintain strong documentation standards and technical writing qualityCommunicate investigation progress and outcomes to relevant stakeholders Bachelor’s degree in chemistry, biotechnology, life sciences or a related fieldExperience with Deviations and cGMP in a regulated pharmaceutical or API environment is a strong advantageKnowledge of biotech manufacturing processes and analytical methods is an advantageExperience with Human and Organizational Performance and risk management approaches is beneficialFluency in English in both written and spoken form; German is an advantageStrong technical writing, analytical and communication skillsStructured, focused and well-organised working styleOpen-minded, agile, highly motivated and adaptable to changeStrong interpersonal and collaboration skills with a proactive mindsetAbility to manage multiple investigations simultaneously in a dynamic environment Opportunity to work in a state-of-the-art large-scale mammalian manufacturing environmentExposure to cross-functional teams and complex deviation management processesImpactful role with high visibility in quality and operations functionsInclusive, international and collaborative workplace culture Ihr Kontakt Referenznummer 863146/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Maintain and troubleshoot data integration pipelines to ensure stable data flow into AI and analytics systemsSupport model development by assisting with training, validation, and optimization of machine learning workflowsConduct data analysis to extract insights and provide clear reports supporting R&D research questionsSolve technical challenges related to data access, pipeline performance, and software limitationsEnsure continuity of ongoing projects by aligning closely with the core team and delivering on timelinesPerform image analysis and prepare datasets required for scientific and ML use casesManage and improve ETL processes to ensure data quality, structure, and availabilityDocument workflows, pipeline changes, and analytical steps to ensure clarity and reproducibility Academic background in computer science, data science, engineering, or a related quantitative fieldStrong proficiency in Python with expertise in scientific and analytical librariesSkilled in SQL and working with relational databasesUnderstanding of ETL concepts and practical experience working with data pipelinesSolid foundation in machine learning principles and model lifecycleAbility to perform image analysis for scientific or research applicationsStrong communication and interpersonal skills with the ability to collaborate in a technical teamIndependent, structured problem-solver with a commitment to clear documentation and FAIR data practices Opportunity to contribute directly to active R&D projects with immediate real-world impactHands-on involvement in AI, machine learning, and data integration challenges in a scientific environmentClose collaboration with a small, highly skilled technical team Ihr Kontakt Referenznummer 863771/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Lead and continuously improve the GMP self-inspection program, including annual planning and executionCoach SMEs and audit teams to ensure strong inspection and self-inspection readinessPerform gap assessments on global procedures and drive alignment across site functionsCoordinate cross-functional activities and ensure effective communication with all departmentsSupport internal, external, and mock audit preparation, including document review and QA inputAct as backroom/ACC or scribe team member during audits and inspectionsServe as Data Integrity Champion and ensure consistent DI implementation across the sitePrepare and present compliance topics to the Quality Council and site leadershipSupport continuous improvement initiatives and coordinate operational activities within the compliance teamAct as back-up for the Quality Compliance & Systems Expert when required University degree in biochemistry, chemistry, engineering, or another relevant scientific/technical disciplineSolid experience in biotechnology and/or pharmaceutical industryStrong knowledge of GMP requirements and Quality SystemsUnderstanding of manufacturing, QC laboratory, and warehouse processes for biological productsSolid knowledge of Good Documentation Practices (GDDP) and Data Integrity principlesExperience supporting audits and regulatory inspectionsSkilled in writing, reviewing, and updating SOPs and technical documentationFamiliarity with risk management tools (FMEA, RCA, etc.)Proficiency in French and English (minimum B2)Experience with eQMS tools (e.g., Veeva Vault, TrackWise), Microsoft Office, SharePoint, and Power BI A very renowned companyContinuous support during the assignmentIndividual all-round care: Support throughout the entire application phase Ihr Kontakt Referenznummer 864224/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
-Ing., or higher)Solid proven project management and leadership experience in mid-sized, complex CapEx projects within the chemical, biotech, or pharmaceutical industryStrong project management skills, including expertise in contract management, cost control, and stakeholder managementDemonstrated experience in process and infrastructure engineering in chemical, biotech, or pharmaceutical environmentsSolid understanding and practical experience with cGxP requirements as well as qualification and validation processesFluent in German and English, both written and spokenProven leadership capabilities with the ability to guide teams and manage departmental responsibilities A highly motivated team and an open way of communication A very renowned companyGood infrastructurePossibilities to work remoteTips on how to prepare a successful application Ihr Kontakt Referenznummer 865168/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
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
Register now and look forward to many interesting and suitable positions and projects. Mein Arbeitgeber Our client is a globally recognized leader in the medical technology and diagnostics industry. The Rotkreuz site focuses on the development and testing of advanced laboratory instruments used worldwide in highly regulated environments.
At Oxford Instruments, our commitment to our customers is paramount; this position is pivotal in ensuring the quality, accuracy, and timeliness needed to exceed our customers’ expectations. What You'll Do: Publish customer manuals: Use Framemaker and Flare to create bespoke customer manuals from existing content.
Create your future by joining our Graduate Trainee Program where you will have the opportunity to work on a full-time contract position for18-months. Upon successful completion of theprogram,you stand a chance to be shortlisted for exciting job opportunities based on your career aspirations, your performance and also on business needs and available vacancies.
JOIN OUR TEAM IN COLOGNE FOR A FULL-TIME POSITION, STARTING AS SOON AS POSSIBLE. Expert “Automation Designer (m/f/x)” in the Center of Digitization DO YOU HAVE PLENTY OF KNOWLEDGE AND WANT TO MAKE A DIFFERENCE?
JOIN OUR TEAM IN BONN (GERMANY) FOR A FULL-TIME (40 HOURS PER WEEK) POSITION, STARTING AS SOON AS POSSIBLE. Global Customer Manager (M/F/X) TODAY, YOU’RE STIMULATING THE WAY A CUSTOMER SUCCEEDS. TOMORROW, YOU’RE SHAPING THE WAY THE WORLD WORKS.
Performs testing of samples linked to operations, validation, utilities and environmental monitoring samples Coordinate and work on the transfer, development and validation of analytical methods including qualification of equipment needed for analysis Coordination in maintenance, calibration and use of laboratory equipment Actively contribute to the GMP Inspection Readiness of QC to ensure the fully compliance of relevant Quality System and Procedural documents Actively contribute to the QC operational readiness managing projects (external and internal) and the assigned to ressources (including coordination of people daily tasks) Participates in the transfer, development and validation of analytical methods including qualification of equipment needed for analysis Creation and revision of guidance documents such as SOPs/ WIs and other related documents Master’s degree or higher in Life Sciences, Chemistry, Biochemistry, or a related scientific field (lower educational background acceptable with relevant experience) Solid experience in chemical or biochemical laboratories, including work in a regulated GMP environment Experience performing analytical testing of samples related to operations, validation, utilities, and environmental monitoring Strong expertise in analytical method transfer, development, and validation Experience with qualification, maintenance, and calibration of analytical laboratory equipment Solid understanding of GMP regulations, quality systems, and inspection readiness within QC laboratories Experience in creating and revising SOPs, work instructions, and other quality documentation Ability to coordinate QC activities and support operational readiness projects in laboratory environments Strong collaboration and communication skills, working effectively across cross functional teams Demonstrated ability to drive results, adapt quickly to changing situations, and maintain a strong business and quality focus Renowned pharmaceutical company Attractive salary package HAYS Benefits Ihr Kontakt Referenznummer 864632/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register now and look forward to many interesting and suitable positions and projects. Working in an interdisciplinary team of engineers to develop and improve designs and manufacturing processes for thick film sensors Improve and maintain the data infrastructure and pipeline for production and process control data from various sources and ensure timely data availability Act as a technical interface between R&D and Production and between various R&D departments to harmonize data handling and standards Improve and maintain data visualization tools (dashboards, interactive charts) and support in routine data analysis Support in defining and improving image analysis methods and tools to derive quantitative feature values from images Extend the data infrastructure with additional information, e.g. from sensor performance characterization Data driven improvements of manufacturing processes Completed technical training in process engineering, data science, bioinformatics, or similar professional education Professional experience in industrial R&D or manufacturing environment, ideally in the medical device industry or a comparable regulated environment Experience in building and maintaining data pipelines (ETL processes) from diverse sources such as SQL databases, CSV, and machine log files Ability to create interactive dashboards and visualization tools with a solid understanding of applied statistics (e.g. correlation analysis, cluster analysis) to support the development teams Skills in digital image processing, object-oriented programming (OOP) in Python, and knowledge of SQL are a strong advantage, adding significant value to this opportunity Good communication skills in a multicultural and multidisciplinary environment A thorough way of working and documentation Motivated team player with passion in promoting and driving fast-paced and ambitious projects Aptitude to understand and improve the underlying technical processes Proficiency in both English and German Unlimited project contract Fascinating, innovative environment in an international atmosphere Ihr Kontakt Ansprechpartner Jannik Fabio Eichin Referenznummer 865639/1 Kontakt aufnehmen E-Mail: jannik.eichin@hays.ch Anstellungsart Freiberuflich für ein Projekt
Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis models Execute full end-to-end in vivo workflows, from study preparation to sample processing and documentation Characterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assays Handle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experiments Perform data analysis, interpret results, and present findings to the research team Maintain accurate, complete, and compliant documentation across all experimental steps Contribute to lab operations, including safety standards, inventory, equipment handling, and general organization Collaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experience Active certification for animal experimentation (e.g., LTK1, FELASA, or equivalent) Proven hands-on experience with rodent work, including intravenous injections and blood sampling Ability to independently design, execute, and manage in vivo studies from start to finish Experience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapy Strong ability to plan experiments, analyze data, and interpret scientific results Fluency in English with clear communication skills Highly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impact Hands-on work with a combination of in vivo, ex vivo, and molecular biology techniques Collaborative environment with close teamwork and modern laboratory infrastructure Diverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Sollten wir danach gemeinsam zum Ergebnis gelangen, dass diese Position gut zu Ihren Zielen passt, schicken Sie uns die restlichen Unterlagen (Zeugnisse, Zertifikate, bei Bedarf Referenzen). Danach werden wir Sie Sie bei unserem Mandanten vorstellen, mit Ihrem Einverständnis.
The CIMH strives to increase the proportion of women in all areas and positions where women are underrepresented. Qualified women are therefore particularly encouraged to apply. Full-time positions can generally be split, provided that there are no operational or legal reasons preventing this.
You know how to turn a first conversation into real pipeline and transform customer interest into committed revenue. You understand what retailers are looking for and you position our solutions so persuasively that choosing us becomes the obvious business decision. With Retail7, GK Software’s cloud‑native commerce platform, you open doors, generate demand, and accelerate the path to “yes.”
You will find on our homepage https://www.dpdhl.jobs/grow-program more detailed information on the application process, program schedule and typical project positions in the various business areas. We are looking forward to your application. CONNECTING PEOPLE. IMPROVING LIVES. #growprogram #growhr
You will find on our homepage https://www.dpdhl.jobs/grow-program more detailed information on the application process, program schedule and typical project positions in the various business areas. We are looking forward to your application. CONNECTING PEOPLE. IMPROVING LIVES. #growprogram #growbds
Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical softwareEnsure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomesCommunicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teamsEmpower your team members to take ownership of their work and leading by example to foster teamwork and mentorship Degree or equivalent practical experience in a specialized field related to software development or engineeringProven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx).Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis to resolve complex technical challengesExcellent communication skills with the ability to foster an inclusive and diverse environment as well as collaborate effectively within and across teamsEnglish fluency is a prerequisite, German is advantageous Internal career opportunitiesWorld-renowned medical devices company Ihr Kontakt Referenznummer 858105/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register now and look forward to many interesting and suitable positions and projects. Analyze system requirements and assess the feasibility of testing in simulated environments as well as in vehiclesDesign and develop test cases for system requirements, particularly for IVI systems including navigation, telematics, and streaming servicesExecute integrated system tests on test benches and in-vehicle environmentsTake ownership of key test milestones, such as quality audits and final release gate checks for new vehicle platformsCollaborate closely with Tier-1 suppliers and coordinate activities with our R&D headquarters in KoreaTrack issues and manage bug fixes using JIRA, ensuring alignment with vehicle line timelines and software release planReview and challenge technical solutions with a focus on system performance and market competitivenessIdentify improvement opportunities based on European market trends and actively support their implementation Bachelor’s or Master’s degree in Computer Science, Engineering, Electrical Engineering, or a related fieldPractical experience conducting driving tests within the EU region, ideally in the area of automotive infotainment validationExperience in system validation, preferably covering navigation, connected car services, and streaming applicationsFamiliarity with configuration management and version control toolsBasic knowledge of data analytics is an advantageStrong planning and organizational skills with a structured working approachHigh level of flexibility and motivation to work in an international and cross-cultural environmentVery good command of the English language, both written and spokenWillingness to travel and conduct driving tests; valid European driving license (Category B) required Pleasant working atmosphereChallenging and varied tasks in a promising and innovative industryDynamic and innovative market environmentA highly motivated team and an open communication styleAngenehmes Arbeitsklima Ihr Kontakt Ansprechpartner Annika Chrysant Referenznummer 858521/1 Kontakt aufnehmen E-Mail: annika.chrysant@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Performs testing of samples linked to operations, validation, utilities and environmental monitoring samplesCoordinate and work on the transfer, development and validation of analytical methods including qualification of equipment needed for analysisCoordination in maintenance, calibration and use of laboratory equipmentActively contribute to the GMP Inspection Readiness of QC to ensure the fully compliance of relevant Quality System and Procedural documentsActively contribute to the QC operational readiness managing projects (external and internal) and the assigned to ressources (including coordination of people daily tasks)Participates in the transfer, development and validation of analytical methods including qualification of equipment needed for analysisCreation and revision of guidance documents such as SOPs/ WIs and other related documents Master’s degree or higher in Life Sciences, Chemistry, Biochemistry, or a related scientific field (lower educational background acceptable with relevant experience)Solid experience in chemical or biochemical laboratories, including work in a regulated GMP environmentExperience performing analytical testing of samples related to operations, validation, utilities, and environmental monitoringStrong expertise in analytical method transfer, development, and validationExperience with qualification, maintenance, and calibration of analytical laboratory equipmentSolid understanding of GMP regulations, quality systems, and inspection readiness within QC laboratoriesExperience in creating and revising SOPs, work instructions, and other quality documentationAbility to coordinate QC activities and support operational readiness projects in laboratory environmentsStrong collaboration and communication skills, working effectively across cross functional teamsDemonstrated ability to drive results, adapt quickly to changing situations, and maintain a strong business and quality focus Renowned pharmaceutical company Attractive salary package HAYS Benefits Ihr Kontakt Referenznummer 864632/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
. +45 2917 1009, email: mga@foodjobnordic.com can be contacted for further information on the position. Foodjob Nordic ensures absolute discretion for all applicants.
Essential Functions Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.Develop contract language, payment language and budget templates as required as applicable to the positionUtilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreementsReport contracting performance metrics and out of scope contracting activities as required.Work with Quality Management to ensure appropriate contract management and quality standards.
Register now and look forward to many interesting and suitable positions and projects. Working in an interdisciplinary team of engineers to develop and improve designs and manufacturing processes for thick film sensorsImprove and maintain the data infrastructure and pipeline for production and process control data from various sources and ensure timely data availabilityAct as a technical interface between R&D and Production and between various R&D departments to harmonize data handling and standardsImprove and maintain data visualization tools (dashboards, interactive charts) and support in routine data analysisSupport in defining and improving image analysis methods and tools to derive quantitative feature values from imagesExtend the data infrastructure with additional information, e.g. from sensor performance characterizationData driven improvements of manufacturing processes Completed technical training in process engineering, data science, bioinformatics, or similar professional educationProfessional experience in industrial R&D or manufacturing environment, ideally in the medical device industry or a comparable regulated environmentExperience in building and maintaining data pipelines (ETL processes) from diverse sources such as SQL databases, CSV, and machine log filesAbility to create interactive dashboards and visualization tools with a solid understanding of applied statistics (e.g. correlation analysis, cluster analysis) to support the development teamsSkills in digital image processing, object-oriented programming (OOP) in Python, and knowledge of SQL are a strong advantage, adding significant value to this opportunityGood communication skills in a multicultural and multidisciplinary environment A thorough way of working and documentationMotivated team player with passion in promoting and driving fast-paced and ambitious projectsAptitude to understand and improve the underlying technical processesProficiency in both English and German Unlimited project contractFascinating, innovative environment in an international atmosphere Ihr Kontakt Ansprechpartner Jannik Fabio Eichin Referenznummer 865639/1 Kontakt aufnehmen E-Mail: jannik.eichin@hays.ch Anstellungsart Freiberuflich für ein Projekt
Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis modelsExecute full end-to-end in vivo workflows, from study preparation to sample processing and documentationCharacterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assaysHandle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experimentsPerform data analysis, interpret results, and present findings to the research teamMaintain accurate, complete, and compliant documentation across all experimental stepsContribute to lab operations, including safety standards, inventory, equipment handling, and general organizationCollaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experienceActive certification for animal experimentation (e.g., LTK1, FELASA, or equivalent)Proven hands-on experience with rodent work, including intravenous injections and blood samplingAbility to independently design, execute, and manage in vivo studies from start to finishExperience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapyStrong ability to plan experiments, analyze data, and interpret scientific resultsFluency in English with clear communication skillsHighly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impactHands-on work with a combination of in vivo, ex vivo, and molecular biology techniquesCollaborative environment with close teamwork and modern laboratory infrastructureDiverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Proficiency in French and English (minimum B2) Experience with eQMS tools (e.g., Veeva Vault, TrackWise), Microsoft Office, SharePoint, and Power BI A very renowned company Continuous support during the assignment Individual all-round care: Support throughout the entire application phase Ihr Kontakt Referenznummer 864224/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Create your future by joining our Graduate Trainee Program where you will have the opportunity to work on a full-time contract position for 18-months. Upon successful completion of the program, you stand a chance to be shortlisted for exciting job opportunities based on your career aspirations, your performance and also on business needs and available vacancies.
Create your future by joining our Graduate Trainee Program where you will have the opportunity to work on a full-time contract position for 18-months. Upon successful completion of the program, you stand a chance to be shortlisted for exciting job opportunities based on your career aspirations, your performance and also on business needs and available vacancies.
Create your future by joining our Graduate Trainee Program where you will have the opportunity to work on a full-time contract position for 18-months. Upon successful completion of the program, you stand a chance to be shortlisted for exciting job opportunities based on your career aspirations, your performance and also on business needs and available vacancies.
Severely disabled applicants will be given preference if equally qualified. This position can be full-time or part-time (min. 30h/week). DKV Mobility is looking for the best talents and knows that these are not always available on a full-time basis.
Severely disabled applicants will be given preference if equally qualified. This position can be full-time or part-time (min. 30h/week). DKV Mobility is looking for the best talents and knows that these are not always available on a full-time basis.