Independent design of control and protection systems for high-voltage direct current (HVDC) transmission systemsImplementation of control software in MATLAB/SIMULINK and verification using simulation tools and real-time test environmentsPreparation of related design specifications, documentation, and effort estimationsClarification of technical requirements within project teams as well as with customers and suppliersRemote support during commissioning and in service cases Completed university degree in Electrical Engineering with a focus on power engineering or control engineering, along with relevant professional experienceStrong knowledge of converter and high-voltage technology, as well as plant, control, and automation engineeringSolid MATLAB/SIMULINK skills, including model-based implementation and verificationExperience in engineering automation systems, preferably SIMATIC TDC / S7Very good command of EnglishGerman language skills desirable You benefit from exclusive access to interesting companies and exciting projects in cooperation with Hays as a solid and stable partnerRemuneration in accordance with the industry collective agreement (GVP)Annual vacation entitlement of 30 daysWorking time account with the option of overtime pay or time off in lieuProfessional and trusting cooperation Ihr Kontakt Referenznummer 860505/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Support procurement processes across all Carve-out phases including due diligence, planning and executionEnsure smooth transition and integration of systems, services and suppliersDevelop and manage strong relationships with key vendors and service providersLead negotiations and manage supplier performance and complianceConduct strategic sourcing and supplier selection based on quality, cost and reliabilityManage contract creation, negotiation and lifecycle governancePerform data analysis to identify cost optimization and process improvement opportunitiesAssess, monitor and mitigate procurement-related risksCollaborate closely with cross-functional stakeholders including IT, Automation, Quality, Finance, Legal and MROMaintain procurement KPIs and develop data-driven performance reports Bachelor’s degree in IT, Business Administration, Supply Chain Management or a related fieldMaster’s degree or relevant certifications (CPSM, CIPS) are an advantageExperience in indirect procurement, ideally in CDMO or pharma environmentsExperience in Carve-out or Divestment activitiesExtensive knowledge in procurement processes, strategic sourcing, vendor and contract managementProven track record in managing procurement streams within business divestmentsStrong negotiation, analytical and problem-solving skillsExcellent communication abilities and stakeholder management skillsProficiency in procurement systems, ERP tools and MS OfficeStrategic thinker, highly organized, adaptable, resilient and collaborative in team settings Opportunity to work on high-impact strategic Carve-out projects within a global CDMOExposure to cross-functional leadership teams and strategic decision-makingInnovative, collaborative and international work environment Ihr Kontakt Referenznummer 863140/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Proven experience managing large budgets, complex projects, and delivering performance against ambitious target Exciting project in a renowned company Ihr Kontakt Referenznummer 865383/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Freiberuflich für ein Projekt
Annika Pohl Personalreferentin & Ausbildungsleitung E-Mail: annika.pohl@wentronic.com Telefon: 0531-21058870
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
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
Schicke uns deine aussagekräftigen Unterlagen mit tabellarischem Lebenslauf, Zeugniskopien, Angaben über Einkommensvorstellungen und frühestmöglichen Eintrittstermin zu. ETS DIDACTIC GMBH Im Hüttental 11 85125 Kinding Telefon: 08467 840449 E-Mail: job@ets-didac tic.de
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
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
-Ing., or higher) Solid proven project management and leadership experience in mid-sized, complex CapEx projects within the chemical, biotech, or pharmaceutical industry Strong project management skills, including expertise in contract management, cost control, and stakeholder management Demonstrated experience in process and infrastructure engineering in chemical, biotech, or pharmaceutical environments Solid understanding and practical experience with cGxP requirements as well as qualification and validation processes Fluent in German and English, both written and spoken Proven 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 company Good infrastructure Possibilities to work remote Tips 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
Klare Weiterentwicklungsperspektive Richtung Head-of-Level Individuelles Onboarding sowie gezielte Zertifizierungen & Trainings Ergebnisorientierte Engineering-Kultur mit blameless Incident-Prinzip Attraktives Vergütungspaket (ca. 85.000-110.000 € je nach Erfahrung) Zusätzliche Benefits innerhalb der Unternehmensgruppe & regelmäßige Team-Events IHR PRIMEPEOPLE PROZESS Schicken Sie uns gerne Ihre Unterlagen oder greifen Sie einfach zum Telefon. Uns ist wichtig, Sie als Mensch kennenzulernen – mit Ihrer Geschichte, Ihren Stärken und Ihren beruflichen Zielen. Denn je besser wir Sie verstehen, desto gezielter können wir Sie auf Ihrem nächsten Karriereschritt begleiten.
Business Fluent in English and German: Effective oral / written communication skills in English (C1) / Oral / written communication skills in German (B2) Good infrastructureA very renowned companyYou will work in an international environment Ihr Kontakt Referenznummer 863189/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Initiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements Create and maintain supplier records in the qualification system Assess material changes and drive required quality change controlsSupport supplier qualification activities and coordinate supplier auditsManage supplier relationships to ensure value delivery and site performanceDevelop material specifications to support qualification and releaseCoordinate material release schedules to secure on-time production supplyCollaborate with tech transfer, procurement, quality, and manufacturing on supplier and material selectionEnsure materials meet required quality grades for clinical manufacturingAlign purchase orders and material planning with lead times, safety, quality, cost, and production schedulesSupport quality investigations, risk assessments, and continuous improvement initiatives including business case development.Bachelor’s or Master’s degree in engineering, pharmacy or science related field or profound experience working in a relevant academic or industry field Renowned pharmaceutical companyLong term contractAttractive salary package25 Days Holiday Ihr Kontakt Referenznummer 863542/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Dein Gesamtpaket umfasst: Attraktive, leistungsgerechte Vergütung mit variablem Anteil Flexible Arbeitszeiten und hybrides Arbeitsmodell Moderne IT-Ausstattung und Remote-Setup Individuelle Weiterbildungs- und Entwicklungsmöglichkeiten Ergebnisorientierte Teamkultur mit Spaß an neuen Herausforderungen Viele Benefits innerhalb der Unternehmensgruppe Regelmäßige Team- und Company-Events – und Kolleg:innen, die gerne gemeinsam Erfolge feiern IHR PRIMEPEOPLE PROZESS Schick uns einfach Deine Unterlagen oder nimm Kontakt auf über Telefon, XING oder LinkedIN. Der Schutz Deiner Daten nach der DSGVO ist sichergestellt. Im ersten Schritt ist es mir wichtig, Dich näher kennenzulernen und Deine Ziele besser zu verstehen.
Dein Gesamtpaket umfasst: Überdurchschnittliches Gehalt mit variablem Bonusanteil Mobilitäts- und Ausstattungspaket (Firmenwagenoption oder Budget) Hybrides Arbeitsmodell mit modernem Remote-Setup Flexible Arbeitszeiten und hohe Eigenverantwortung Individuelle Trainings- und Coachingprogramme Ergebnisorientierte Teamkultur mit Freude an gemeinsamen Erfolgen Umfangreiche Benefits innerhalb der Unternehmensgruppe Mitarbeiterevents & Kolleg:innen, die Zusammenarbeit wirklich leben IHR PRIMEPEOPLE PROZESS Schick uns gerne deine Unterlagen oder greif direkt zum Telefon. Im ersten Schritt geht’s uns darum, dich kennenzulernen und zu verstehen, wohin du beruflich willst. Nach deinem Einverständnis (Datenschutzerklärung) nehmen wir dich gern in unser exklusives Kandidatennetzwerk auf.
Dein Gesamtpaket umfasst: Attraktives Grundgehalt mit variabler Erfolgsvergütung Mobilitäts- und Ausstattungspaket (Firmenwagenoption, Remote-Equipment) Flexible Arbeitszeiten & hybrides Arbeitsmodell Persönliche Weiterentwicklung durch Trainings & Leadership-Coachings Ergebnisorientierte Teamkultur mit Spaß an neuen Herausforderungen Eine Vielzahl an Benefits innerhalb der Unternehmensgruppe Regelmäßige Team- & Company-Events mit Kolleg:innen an vielen Standorten IHR PRIMEPEOPLE PROZESS Schick uns gerne deine Unterlagen oder greif direkt zum Telefon. Im ersten Schritt geht’s uns darum, dich kennenzulernen und zu verstehen, wohin du beruflich willst. Nach deinem Einverständnis (Datenschutzerklärung) nehmen wir dich gern in unser exklusives Kandidatennetzwerk auf.