Ihre Aufgaben: Gesamtverantwortung für Planung, Steuerung und Umsetzung von Architektur-/Bauprojekten im Pharma-/Chemieumfeld Termin-, Qualitäts- und Kostensteuerung; Reporting und Claim/Change-Management Schnittstelle zu Kunden, Behörden, Architekten, Fachplanern und Anlagenbau Führung von Teilprojektteams, Koordination externer Dienstleister Sicherstellung regulatorischer Anforderungen (GMP, HSE, VDI/DIN) Ihr Profil: Studium Architektur/Bauingenieurwesen oder vergleichbar Erfahrung im Industrie- oder Anlagenbau; Pharma/Chemie stark bevorzugt Hoher Freiheitsgrad gewohnt, hands-on, kommunikativ, teamorientiert Gute Kenntnisse GMP/Regulatorik und gängiger PM-Tools (MS Project) Deutsch fließend, Englisch gut Was wir Ihnen bieten: Einen festen Arbeitsvertrag in einem sicheren Unternehmen Mobiles Arbeiten Ein übertarifliches Gehalt, zzgl.
Ihre Aufgaben: Gesamtverantwortung für Planung, Steuerung und Umsetzung von Architektur-/Bauprojekten im Pharma-/Chemieumfeld Termin-, Qualitäts- und Kostensteuerung; Reporting und Claim/Change-Management Schnittstelle zu Kunden, Behörden, Architekten, Fachplanern und Anlagenbau Führung von Teilprojektteams, Koordination externer Dienstleister Sicherstellung regulatorischer Anforderungen (GMP, HSE, VDI/DIN) Ihr Profil: Studium Architektur/Bauingenieurwesen oder vergleichbar Erfahrung im Industrie- oder Anlagenbau; Pharma/Chemie stark bevorzugt Hoher Freiheitsgrad gewohnt, hands-on, kommunikativ, teamorientiert Gute Kenntnisse GMP/Regulatorik und gängiger PM-Tools (MS Project) Deutsch fließend, Englisch gut Was wir Ihnen bieten: Einen festen Arbeitsvertrag in einem sicheren Unternehmen Mobiles Arbeiten Ein übertarifliches Gehalt, zzgl.
B. in Wirtschaftsingenieurwesen, Internationales Handelsmanagement, BWL, Supply Chain Management oder vergleichbarMehrjährige Berufserfahrung im GMP-regulierten Umfeld, idealerweise in der Pharmaindustrie oder pharmazeutischen Distribution z.B. als Compliance Manager, Regulatory Compliance Manager, GMP Compliance Manager / GMP Specialist, Project Manager / PMO Manager Quality & Compliance (m/w/d)Fundierte Kenntnisse in GxP, Quality Management, CAPA, Change ControlErfahrung im Projektmanagement (PMO-Strukturen)Sicherer Umgang mit SAP (idealerweise SAP BI) und MS OfficeSehr gute Deutsch- und Englischkenntnisse WIR GARANTIEREN IHNEN: Sie erwartet eine direkte Festanstellung bei unserem wertschätzenden Kunden.Um Sie bestmöglich bei unserem Kunden zu präsentieren, optimieren wir gemeinsam Ihre Bewerbungsunterlagen und bereiten Sie gründlich auf das Vorstellungsgespräch im Unternehmen vor.Damit Sie zu den besten Konditionen eingestellt werden, stehen wir Ihnen im Voraus zur Verhandlung Ihres Arbeitsvertrags beratend zur Seite.Darüber hinaus beraten wir Sie auch gern kostenfrei zu weiteren passenden Karrieremöglichkeiten.
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
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
Register now and look forward to many interesting and suitable positions and projects. Coordinate activities within the transformation program across defined workstreams Refine program scope, timelines, and budget as required Prepare materials and documentation for steering committee meetings Maintain RAID logs, coordinate project related communication and escalations with stakeholders Prepare decision proposals and support the transparent execution of the program Ensure all program activities comply with regulatory requirements and quality standards (e.g., GMP, GAMP, ISO standards) Apply established methods and tools for quality assurance and project coordination (e.g., SAP, QMS, TrackWise, CAPA) Align with multiple stakeholders, including senior managers and subject matter experts, to ensure successful program delivery Knowledge in GMP Knowledge in GAMP Knowledge in SAP Knowledge in QMS Knowledge in TrackWise Knowledge in CAPA Possibility of extending the project Ihr Kontakt Ansprechpartner Daniel Grudentaler Referenznummer 865825/1 Kontakt aufnehmen E-Mail: daniel.grudentaler@hays.de Anstellungsart Freiberuflich für ein Projekt
Flexible working hours; Access to public transportation; Multiple career opportunities; Trust-based working time Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future. Do you want to be successful with us? Then, please send us your application: SCHOTT Pharma AG & Co.
Act as the single point of contact for the day-to-day management of the finite schedule managing shop floor manufacturing and facility activities Coordinate between operations, process engineering, automation, facility engineering, microbiology and other related functions to govern what happens within the process area Attend daily tier meetings (Tier 1 and Tier 2) Update the schedule daily Align the Site Plan of Record with the Finite Schedule to ensure consistency and accuracy and work closely with technology transfer to project the scenarios of new product introduction and proactive planning of new activities Enable the seamless execution of activities encompassing objectives of Manufacturing, Process Engineering, Plant Engineering, Calibrations, Lab, and Warehouse operationWork with network experts to develop a road map to fully deploy RTMS functionality to enable increase facility capacity utilization and resource assignment and evaluation Fully build out RTMS operations models for fed batch and continuous manufacturing paradigms Collaborate cross functionally to performing debottlenecking exercises and partnering with Manufacturing Technology and Strategy on Capacity Ramp and Utilization Strategy Support the assessment of unforeseen events to the schedule and create mitigation plans Ensure accountability for schedule adherence, take ownership and escalation when issues arise.
Act as the single point of contact for the day-to-day management of the finite schedule managing shop floor manufacturing and facility activitiesCoordinate between operations, process engineering, automation, facility engineering, microbiology and other related functions to govern what happens within the process areaAttend daily tier meetings (Tier 1 and Tier 2)Update the schedule dailyAlign the Site Plan of Record with the Finite Schedule to ensure consistency and accuracy and work closely with technology transfer to project the scenarios of new product introduction and proactive planning of new activitiesEnable the seamless execution of activities encompassing objectives of Manufacturing, Process Engineering, Plant Engineering, Calibrations, Lab, and Warehouse operationWork with network experts to develop a road map to fully deploy RTMS functionality to enable increase facility capacity utilization and resource assignment and evaluationFully build out RTMS operations models for fed batch and continuous manufacturing paradigmsCollaborate cross functionally to performing debottlenecking exercises and partnering with Manufacturing Technology and Strategy on Capacity Ramp and Utilization StrategySupport the assessment of unforeseen events to the schedule and create mitigation plansEnsure accountability for schedule adherence, take ownership and escalation when issues arise.
Register now and look forward to many interesting and suitable positions and projects. Coordinate activities within the transformation program across defined workstreamsRefine program scope, timelines, and budget as requiredPrepare materials and documentation for steering committee meetings Maintain RAID logs, coordinate project related communication and escalations with stakeholders Prepare decision proposals and support the transparent execution of the program Ensure all program activities comply with regulatory requirements and quality standards (e.g., GMP, GAMP, ISO standards) Apply established methods and tools for quality assurance and project coordination (e.g., SAP, QMS, TrackWise, CAPA) Align with multiple stakeholders, including senior managers and subject matter experts, to ensure successful program delivery Knowledge in GMPKnowledge in GAMPKnowledge in SAPKnowledge in QMSKnowledge in TrackWiseKnowledge in CAPA Possibility of extending the project Ihr Kontakt Ansprechpartner Daniel Grudentaler Referenznummer 865825/1 Kontakt aufnehmen E-Mail: daniel.grudentaler@hays.de Anstellungsart Freiberuflich für ein Projekt
Fundiertes Wissen im Projektmanagement (Zertifizierung nach IPMA, PMI oder vergleichbar sind von Vorteil Erfahrung mit CAFM-Systemen und MS Project oder vergleichbaren Projektmanagement-Tools Sie überzeugen persönlich durch: ausgeprägte analytische und konzeptionelle Fähigkeiten hohe Technikkompetenz verbunden mit wirtschaftlichem Denken sichere Kommunikations- und Präsentationsfähigkeiten Durchsetzungsstärke und sicheres Auftreten strukturierte und selbstständige Arbeitsweise Belastbarkeit und Flexibilität Teamfähigkeit und interkulturelle Kompetenz Sichere Deutsch- und Englischkenntnisse in Wort und Schrift Unser Angebot Internationales Arbeitsumfeld Ein attraktives Gehalt Betriebliche Altersvorsorge Aufstiegs- und Entwicklungsmöglichkeiten Viel Austausch mit Ihren Kunden und erfahrenen Kollegen Die Sicherheit eines großen Unternehmens und eine langfristige Zusammenarbeit JLL mitgestalten Wir freuen uns auf Ihre Bewerbung unter Angabe Ihres frühestmöglichen Starttermins sowie Ihrer Gehaltsvorstellung.
Further training and education; Exclusive employee benefits/discounts; Extended vacation entitlement; Holistic corporate health management; Medical, Dental and Vision coverage; Multiple career opportunities; Talent development; Team Events; Trust-based working time; paid vacation days, holidays and sick time Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future. Do you want to be successful with us? Then, please send us your application: SCHOTT ASIA IT SERVICES, Human Resources, Wei Ni Tang, *At SCHOTT, it’s your personality that counts – not your gender, your identity, or origin.Your Profile Bachelor Degree in Computer Science, Business Informatics, or a comparable field.3 years of experience in operating production services and operational services, initial experience in dealing with service providers and advising customersExperience with MES systems (e.g., HydraX, Cronetwork).Proficiency with monitoring and logging tools (Grafana, Kibana).Linux expertise (Debian preferred).Scripting and automation (Bash, Python, Perl).Networking fundamentals and integration knowledge.Containerization (Docker, Kubernetes) and CI/CD pipelines.Virtualization and cloud technologies (VMware, KVM, Azure).SQL database knowledge.Initial experience with service providers and customer advisory.Strong communication skills and knowledge of application management processes.Understanding of business processes in smart factory contexts.Familiarity with service management methods (PMI & ITIL).Proficiency in English.