Gehaltsübersicht für Data Quality Manager in Aargau

Project Manager Wind - Delivery, Commissioning and Warranty (m/f/d) - (80%-100%)Take your next career step at ABB with a global team that is energizing the transformation of society and industry to achieve a more productive, sustainable future. At ABB, we have the clear goal of driving diversity and inclusion across all dimensions: gender, LGBTQ+, abilities, ethnicity and generations. Together, we are embarking on a journey where each and every one of us, individually and collectively, welcomes and celebrates individual differences.Are you keen to take ownership of wind projects – of large scope – covering the project phase between delivery to factory and end of warranty? This is your chance to help shape our business as Project Manager in the growing offering in Wind. In this role, you will be fully responsible for the successful delivery, installation, testing and commissioning of wind converters as well as the effective management of warranty cases and lifecycle services to key accounts. This will also include ensuring that targets relating to deadlines, costs, and other specific goals are met. Additionally, your duties will encompass coordination of different experts in this phase, reporting, content, scope and change management, and issues such as project-related risks, business opportunities and procurement. This position reports to Global Business Developmnt Mgr Packaging Your responsibilities Take partly commercial and full technical responsibility for your projects and manage effective structuring, planning, budgeting, and execution from delivery until end of warranty Ensure that all contractual requirements are met while establishing and maintaining a fruitful relationship with our key customers and their needs and operations. Take responsibility for the achievement of commercial targets (revenue, cash flow, NWC, margins) Establish a commissioning team with resources from ABB hubs and suppliers, ensure a smooth operation of the team Ensure that Health & Safety and Quality standards are met, which will also include setting up Health & Safety plans Monitor projects and execute regular reporting (from time sheet to field service report) Repeated presence on customer sites worldwide may be needed to ensure own field services can progress fluently and effectively Optimize use of resources, including those in local organizations Contribute to internal improvement projects and ensure they are implemented in accordance with Lean Six Sigma methodology Your background Degree in Engineering, Mechanical or Electrical Engineering, and experience in managing customer projects especially covering field services. Experiences working on project sites will be an advantageous asset. Knowledge of power converters as well as experience in managing commissioning and warranty cases for such components With your customer focus and leadership skills you contribute to the success of your projects. You have a very positive attitude towards challenges and change and appreciate explicitly to contribute to this. You want to improve your work environment continuously in line with the strategy of your business area Ability to work successfully in a complex organization Proven track record in contract and claims management Knowledge of site administration (permit to work, gate access etc.) Strong command of English, good French or German skills are a definitive asset, other language skills too Well-developed communication skills and mindset needed to work within an international team and provide professional and timely responses to queries Assertiveness, results-oriented approach, and excellent analytical abilities Availability to travel up to 50% More about us ABB System Drives is a global supplier of high-power, high-performance drives, drive systems and packages for industrial processes and large infrastructure applications. With our industry leading technology and global support, we help our customers, partners and equipment manufacturers with asset reliability, performance improvement and energy efficiency in mission critical applications. Our people and culture are the foundation of our success. We all together make the difference for our customers every day. We look forward to receiving your application (documents submitted in English are appreciated). The recruiting process is being led by Peter Reinhardt, Talent Partner ABB Switzerland Ltd. If you want to discover more about ABB, take another look at our website www.abb.com. ABB Data Privacy Statement: https://new.abb.com/privacy-notice/candidate Work model: hybrid #LI-hybrid

Production Quality Manager Rotor & Generator (m/f)JOB DESCRIPTION Job Description Summary The Production Quality Manager for Rotors and Generator is overall accountable for Quality matters in the Birr Rotor and Generator shop.The individual taking this role will establish a close collaboration with various local and global functions (Manufacturing, Procurement, Planning, Engineering and Customers) to ensure excellence in quality throughout the value chain. In this role you will drive quality related activities internally with all GE functions and interface with the customer on all quality related matters within Rotors and Generator. You will also act as a champion and sponsor for continuous improvement activities within the department. Job Description Essential Responsibilities: Lead a team of 6 quality inspectors and 4 apprentices. Ensure that the defined quality requirements are achieved for all projects, and issues are resolved timely to minimize disruption to production plans. Leading quality in daily operational meetings in every level. Resolve non-conformances (NCRs) with a strong sense of urgency. Creation and management of NCRs, creation and follow up of engineering issue resolutions. Coordinate and lead quality inspections within the Rotor department. Represent the company quality function in front of the customer during witness points and visits. Be the main Quality point of contact for internal Customers. Analyze, comment, and approve Project Quality Plans, as well as Inspection and Test plans. Manage, control of overall Quality documentation, provide factory quality documentation as per customer requirements and as per schedule. Leading Root cause analysis on top issues and implementing necessary actions (RCA methodologies, Lessons Learned, etc.) to create sustained process improvement. Supporting engineering team where required on product qualification process. Empower team performance, supervise/coach team members and foster a positive culture of continuous improvement. Champion LEAN principles and embrace LEAN, continuously question, and take an active role in the continuous improvement processes. Expertise and strong knowhow on quality KPIs (key performance indicators), respective processes. Responsible to manage, prepare, maintain Quality KPI reporting. Required Qualifications: Technical bachelor’s degree in electrical / mechanical engineering from an accredited university or college. Qualification in Quality Management Systems as Lead Auditor as per ISO 9001, etc. Experience in power generation industry in Quality, Manufacturing, Continuous Improvement, Lean, or relevant function. Strong knowledge about inspection and testing of power plant equipment (Generator knowledge will be considered a bonus). Experience and training in Root Cause Analysis tools (e.g., 8D, Apollo, 5-Whys, etc.) Strong EHS (Environmental & Health and Safety) mindset SAP/PMX/Power Now/Fiori /SDR/ NCR process expertise is a must Process Auditor skills & Certification Fluent in English and German Desired Characteristics: Excellent communication skills, including working with large organizations and various levels of leadership. Able to present key data effectively and clearly. Highly motivated self-starter with initiative and strong interpersonal and leadership skills to direct cross-functional work. Ability to coordinate several projects simultaneously. Open mindset with a willingness to understand different perspectives and work collaboratively. Continuous Improvement expertise and experience Effective time management skills & prioritizing ability Ability to influence others. Effective problem identification and solution skills Ownership of quality assurance and quality control, with specific focus on customer interface excellence, operational excellence, and supplier excellence. #LIAA2 #QUALITY#MANAGER#AUDITOR#LEADERHIP#LEANB#BIRR#SWITZERLAND Additional Information Relocation Assistance Provided: No

Manager Qualifizierung, Prozessautomation & CSV (m/w/d)Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters. The Position In der Pharma Produktion Kaiseraugst werden die sterilen Arzneiformen Flüssigvials, Fertigspritzen, lyophilisierte Vials hergestellt sowie ein pulverförmiges Antibiotikum in Vials abgefüllt und verpackt. Mission Statement: Durch wissenschaftlich fundierte Verbesserungen und robustere Prozesse stellen wir einen Wertzuwachs für die Mitarbeiter, Kunden und Patienten sicher. Zusammen wollen wir mit innovativer Sicht weit über den Tellerrand hinausschauen, um durch die Erhöhung der Anlagenverfügbarkeit, Compliance sowie Kostenreduktion die Wettbewerbsfähigkeit sicherzustellen. Im Bereich ES&T (Engineering Science & Technology) Enabling Science & Operational Support bist Du als Qualifzierungs Manager-/in im Wesentlichen für die nachfolgenden Tätigkeiten verantwortlich: Erstellung und Pflege von GMP Dokumenten mit dem Schwerpunkt Prozessautomations Qualifizierung und Computer System Validation sowie Überarbeitung von GMP-Dokumenten (z.B. SOP’s, Rationalen, Risikoanalysen, Testplänen- und Berichten, DI-Assessments etc.) Durchführung der dazugehörigen Tests und Dokumentation im elektronischen Tool “Eval Roche” der Firma ValGenesys Kontinuierliche Verbesserung der bestehenden Prozesse und zugehörigen Dokumenten Sicherstellung des GMP gerechten Lifecycles mittels Change Control- und Abweichungs Prozesses in VEEVA Einhaltung der Data Integrity und CSV Anforderungen in enger Zusammenarbeit mit Quality, für den Standort Kaiseraugst Teilnahme in lokalen und standortübergreifenden Experten-Teams und von Factory Acceptance Test bei unseren Lieferanten Leitung von Projekten oder Teilprojekten im Bereich Prozessautomations Qualifizierung und CSV sowie präsentatieren der Fachbereiche bei Audits und Behördeninspektionen Du arbeitest dabei eng mit den jeweiligen Bereichen wie den Value Streams, PLANTS, der Qualitätssicherung, dem Engineering, ITOT, Materials Management und ES&T-APV zusammen. Wer Du bist Du besitzt eine Ausbildung als Bachelor oder Master, mit dem Schwerpunkt Automation, Pharma-, Biotech-, Verfahrenstechnik oder einer vergleichbaren Ausbildung. Du bist vertraut mit dem Themengebiet Qualifizierung, Data Integrity und Computer System Validierung und hast Berufserfahrung im pharmazeutischen im Bereich Abfüllanlagen und deren Technologien (z.B. sterile Flüssigabfüllung, Lyophilisation, Verpackungsanlagen, Etikettiere ert.). Du zeichnest dich durch eine strukturierte und selbstständige Arbeitsweise aus. Dein Profil erfüllt darüber hinaus folgende Voraussetzungen: Du bist an der Entwicklung von neuen und innovativen Lösungsansätzen interessiert Offen für neue Ideen, eigeninitiativ und hinterfragst konventionelle Denkmuster - Du schätzt es in einer leistungsorientierten Umgebung zu arbeiten, die von gegenseitigem Respekt, Kommunikation, Diskussion und Zusammenarbeit getragen wird Du verstehst es regulatorische Anforderungen in pragmatische Lösungen zu übersetzen und diese Sachverhalte auf allen Ebenen der Organisation strukturiert, präzise und leicht verständlich zu formulieren Fähigkeit Anforderungen der Value Streams in pragmatische und speditive Lösungen umzuwandeln unter Berücksichtigung der notwendigen Qualität Du arbeitest gerne vor Ort am Standort Kaiseraugst und bist daran interessiert, unsere Produktionsanlagen und Prozesse kennenzulernen und diese kontinuierlich zu verbessern Du liebst Herausforderungen und bist bereit dich auch persönlich kontinuierlich weiter zu entwickeln (Polyvalenz) Teamplayer und vertraut mit dem Arbeiten in Matrix- sowie selbstorganisierten Teams und Projekten Gute Deutsch- und Englischkenntnisse werden vorausgesetzt Who we are At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. Roche Kaiseraugst is a cornerstone of Roche's global production and logistics network. It employs some 1900 people out of the 10,700 employees at our Basel/Kaiseraugst site and is Roche's largest and most innovative packaging facility worldwide. Read more. Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees also benefit from multiple services on site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events. We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche.

Qualification Validation Manager 24008 Qualification Validation Manager 24008 Company information Solvias is an internationally recognized provider of integrated solutions in contract analytical research, development and manufacturing. The company offers a broad spectrum of services and solutions in the Pharmaceutical, Biotech, Medical Device, Cell&Gene Therapy and Cosmetic industries. With headquarters near Basel, Switzerland, over 800 highly qualified employees take pride in putting science at the heart of serving customers to bring safer and better products to market faster. Be part of your challenge: take a big jump and do the change of your life! Job Description Executes establishment and maintenance of Equipment Qualification System for the Operations Ensures proper qualification of equipment/instruments/computerized-systems and method validation/transfer/qualification/verification by guaranteeing adherence to the corresponding regulation requirements Acts as first contact for equipment qualification & maintenance within QA as well as equipment qualification document life cycle management and compliance issues for equipment qualification in shared systems (e.g. LIMS, CDS, ...) Supervises and executes compliance activities including but not limited to releasing method validation/transfer/qualification/verification documents and to assigning GMP status and trending of equipment qualification/re-qualification in relation to supplier qualification, changes, CAPAs, audit observations, vendor change notification Takes care of proper qualification of GMP staff by supervising adherence to GMP trainings as well as of equipment supplier /services by supervising adherence to quality agreements Advises on preparation of service agreements, URS, DQ and qualification documents Keeps track of GMP status of equipment/instruments/ computerized systems Support deviations management and continuous process improvement in the area of responsibility Requirements > 4 years working experience in pharmaceutical industries and GMP controlled environment preferable in Quality Control, Production or Quality Assurance. Very good working knowledge in EU and US GMP regulations relevant for equipment qualification, maintenance, method validation/transfer and corresponding compliance systems Solid know-how in EU and US GMP regulations relevant for computerized systems validation Advanced knowledge in Data Integrity rules and requirements Excellent communication and decision making skills Ability to provide solutions for complex challenges and work independently in a team environment Solution oriented, precise, and organized Good inter-personal skills Energized and open-minded Willingness to learn and carry out new and complex tasks Proactive attitude Excellent in German and English, French is a plus What we currently offer: Our employees are very close to our hearts. At Solvias, you get: a well-structured onboarding program intensive training in the beginning the possibility for further development Furthermore, there are a multiple range of benefits like: flexible working time models 40 hours week at least 28.5 vacation days per year (depending on your age) commuter contribution for using public transport contribution to German and English language courses staff restaurant This job offer is a challenging opportunity in a company that values respect, responsibility, and reliability. At Solvias everyone counts and contributes to the success of the company. We strive to create an environment where we learn from each other and are open to feedback. We do not consider Headhunters / Agencies for this position. Does this appeal to you? Apply now SOLVIAS AG

Wir produzieren innovative und einzigartige Produkte, bei denen Technik und Design vereint werden. Eine Position, die dich in Bezug auf dein Fachwissen herausfordern wird, aber auch die Möglichkeit bietet, die eigenen Ideen einzubringen und selbständig zu handeln. Eine abwechslungsreiche, selbständige und verantwortungsvolle Herausforderung in einem Familienunternehmen, das langfristige Perspektiven eröffnet. Wir bieten dir ein spannendes Arbeitsumfeld in einem erfolgreichen Unternehmen.Du willst mehr über uns und unsere Anstellungsbedingungen erfahren? Du bist nur noch wenige Klicks entfernt – wir freuen uns auf deine Online-Bewerbung über unser Bewerbungstool.Vorneweg: diese Stelle besetzen wir ohne externe Personaldienstleister.Die Mitarbeitenden von STOBAG sind das Rückgrat unseres Unternehmens. Als international tätiges Familienunternehmen gehört die STOBAG Gruppe mit über 700 Mitarbeitenden zu den Marktführern der Branche. Mit viel Eigenverantwortung und gutem Teamgeist arbeiten wir gemeinsam daran, unser in Design und Funktionalität überzeugendes Angebot ständig zu verbessern und auch international weiter zu wachsen. Unsere Kompetenzen liegen in der Entwicklung, der Produktion und im Vertrieb von innovativen Beschattungssystemen, Terrassendächern und Verglasungen. Gemeinsam ist es unsere Vision, Lebensräume wertvoller zu machen und dies über Generationen hinweg.Quality Manager 80 - 100% (m/w/d) Muri, AG DEINE AUFGABENDigitalisierung im Quality Management standortübergreifend vereinheitlichen und vorantreiben Führen und Unterstützen der globalen Prozesseigner beim Erarbeiten von Prozessdokumentationen Leiten von internen und externen (SQS) ISO-Audits Entwickeln des aktuell bestehenden Quality Management hin zu einem Business Excellence Ansatz DEIN PROFILtechnisches Grundstudium mit betriebswirtschaftlichem Verständnis Mehrjährige Erfahrung als Qualitätsmanager inkl. Prozessmanagement idealerweise im Industriesektor Kenntnisse von KVP Methodik und Business Excellence Modellen (z.B. EFQM) lösungsorientierter, selbständiger und verantwortungsbewusster Machertyp mit sehr guten Deutsch- und Englischkenntnissen DEINE PERSPEKTIVE

Wir sind ein hoch innovatives, junges und stark wachsendes Deutschschweizer Unternehmen und gehören im Bereich der metallfreien Zahnimplantat-Systemen zu den technologischen Weltmarktführern. Als Teil der CeramTec-Gruppe führen wir eine hauseigene Entwicklung sowie Produktion und vertreiben unsere hochwertigen Medizinaltechnik-Produkte im In- und Ausland. Für unser aufgestelltes und dynamisches Team im Qualitätsmanagement & Regulatory Affairs suchen wir eine motivierte und engagierte Persönlichkeit, die sich als Quality / Regulatory Affairs Manager engagieren will und zum weiteren Erfolg von unserem Unternehmen beiträgt.Aufgrund des stetigen Wachstums unseres Unternehmens suchen wir per sofort oder nach Vereinbarung an unserem Hauptsitz in der Region Zürich (Spreitenbach) eine(n)Quality Manager Medizintechnik (m/w/d) – 100%Ihre AufgabenIhre Aufgaben In dieser Position sind Sie verantwortlich für die Sicherstellung der Qualität der Produkte in Bezug auf Funktion, Sicherheit und Erfüllung normativen Anforderungen in ihren Entwicklungs- und Herstellungsphasen. Dazu gehören folgende Aufgaben:Mitgestaltung, Pflege, Aktualisierungen und Sicherstellung des Qualitätsmanagementsystems inkl. Prozesslandschaft nach ISO13485 Unterstützung, Prüfung und Mitwirkung bei der Entwicklung neuer und Änderung existierender Produkte und Verfahren mit dem Ziel, dass die Projekte die internen und externen Vorgaben erfüllen Evaluierung von Qualitätsereignissen und Überwachung der korrektiven und präventiven Massnahmen (CAPA Evaluation und Bearbeitung) Durchführung und Überprüfung der Produktfreigaben Anlagenqualifizierung und Prozessvalidierung Mitwirkung im Risikomanagement- und Post Market Surveillance-Team inkl. Betreuung und Koordination der internen und externen Ansprechpartner im Zusammenhang mit der Reklamationsbearbeitung Überwachung der Entwicklungen im Bereich der relevanten Normen, Regularien und Empfehlungen Betreuung und Durchführung von internen und externen Audits Mitwirkung beim Lieferantenmanagement Ihr ProfilErfolgreich absolviertes naturwissenschaftliches / technisches Studium oder eine abgeschlossene Berufslehre mit Weiterbildung in Richtung Qualitätsmanagement Berufserfahrung im Qualitätsmanagement im Medizinproduktebereich (ISO 13485) für Klasse IIa oder höher – vorzugsweise im Startup-/KMU-Umfeld Gute Kenntnisse der gängigen Normen (bspw. ISO 13485, ISO 14971, ISO 10993 etc.) Erfahrung mit Regularien für Medizinprodukte (21 CFR, MDR) Sehr gute Englisch- und Deutschkenntnisse Zuverlässige, pragmatische und lösungsorientierte Arbeitsweise Organisationstalent, Leadership, Eigeninitiative und Durchsetzungsvermögen Unser AngebotHerausforderndes Umfeld in einem innovativen und stark wachsenden Unternehmen Dynamisches, hochmotiviertes und aufgestelltes Team Hoher Grad an Eigenverantwortung und viel Raum für Ihre persönliche Entwicklung Transparente und offene Kommunikation sowie partnerschaftliche Zusammenarbeit Wir bieten Ihnen eine abwechslungsreiche und verantwortungsvolle Tätigkeit in einem innovativen Unternehmen, das auch langfristig Perspektiven eröffnet. Interessiert? Ihre vollständige Bewerbung (Lebenslauf, Motivationsschreiben und Zeugnisse) senden Sie bitte per Email an [email protected] freuen uns auf Ihre Kontaktaufnahme!CeramTec Schweiz GmbHIhre AnsprechpersonHerr Fabian Kuhn, Leiter Personal / Frau Dr. Jennifer Langbein, Leiterin Quality Management CeramTec Schweiz GmbH, Bodenäckerstrasse 5, CH-8957 Spreitenbach, T +41 44 388 36 36 / [email protected]öffentlicht:01 Februar 2024Pensum:100%Vertrag:FestanstellungArbeitsort:SpreitenbachQuality Manager Medizintechnik (m/w/d) – 100% – ZERAMEX Dentalpoint AGQuality Manager Medizintechnik (m/w/d) – 100%

Business Process Manager (all genders)At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. Your role The Business Process Manager in Siegfried's Business Process Management (BPM) team drives active process management during IT projects, defining global process standards and managing key user organizations. This role involves supporting stakeholders, identifying strategic IT project demands, and bridging the gap between business and IT as an IT-Business Partner. Collaboration across functions is key to understanding needs and translating them into project strategy, requirements, or change management. Specific tasks and responsibilities In process management As part of the BPM team, align with key stakeholders within the Siegfried organization to define processes in Siegfried, including mapping using BPMN/L with the relevant business associate. Implementation of active management/optimization of processes, including identifying opportunities for data-mining and other technical process improvement methodologies. As a manager of global key user organizations, support adoption and change management throughout Siegfried for a variety of global systems. Specifically, work to create a sustainable ERP key-user organization and maintain its maturity and continuity. Promote a culture of continuous improvement and drive change management initiatives throughout the organization As an IT-Business Partner Build and maintain sustainable relationships with all departments in Siegfried, including senior management, to support communication and network between IT and the other Siegfried departments. Responsibility for IT-Business partner activities with specific global functions/departments with a focus on: improving communication, strategic partnership, strategic IT-project planning, supporting maintenance of IT-architecture & portfolio overview, facilitation of collaboration across functions for more streamlined IT-system roll-outs. In projects Project facilitation for selected IT projects, including guiding projects through IT-processes (such as project open, scope change, and project close). Project management for selected IT projects (deliver on-time and in-budget projects with realistic timelines based on resource availability and priority) Drive select cross-functional tasks and select organizational tasks in large IT-projects (such as ERP roll-outs) Your profile Education and experience A bachelor's or master's degree in informatics, chemistry or biology, combined with 4+ years of experience in a technical role in the pharmaceutical or CDMO industries OR a doctoral degree in natural sciences (chemistry, biology, physics, etc.) combined with 2+ years of experience in IT or IT-related departments Preferred experience in process management and defining business requirements for IT systems Strongly preferred experience with key user organizations and/or SAP ERP Demonstrated ability to structure and plan large projects and project teams Must have the ability to manage stakeholders and expectations effectively Proven ability to communicate across various organizational levels and backgrounds Personal Strengths Excellent verbal and written communication skills in English; proficiency in German, French, Spanish, or Mandarin would be beneficial Enthusiastic about exploring and learning across various topics and departments, and embraces new experiences openly Strong team-player with a proactive, self-starting approach Possesses acute attention to detail and a problem-solving mindset Familiarity with BPM industry standards Openness to occasional travel for work Our benefits Flexible working hours make it possible to combine family, leisure time and career Parking is available at a reduced rate Health insurance: Discounts of up to 10% on additional insurances with our partners for you and your partner/family Our stock purchase plan is generous and individually tailored Paid breakfast break to foster a healthy working culture. Family allowance: all employees entitled to child and/or education allowances receive an additional monthly family allowance Child allowance: Siegfried AG increases the child allowance by 10% compared to the cantonal statutory rate Individual further training opportunities by arrangement Pension fund: Our company pension fund is attractive and contributions can be arranged individually Staff restaurant / cafeteria: meals at preferential conditions Central location: Close to the train station with very good public transport connections Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. Who we are In the Midst of People's Lives - Across the Globe The Siegfried Group is one of the world's leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers' value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products. What we do in Zofingen Zofingen is the hub of the Siegfried Group. The production facility at our Zofingen headquarters supplies our customers around the globe with exemplary Swiss quality. The Siegfried company is a popular employer in the Zofingen region, where we meet our social responsibility by training apprentices. Main activities Development and commercial manufacture of active pharmaceutical ingredients (APIs) and corresponding intermediates Fully compliant with cGMP and SHE (Safety, Health and Environmental) standards Special features Manufacture of high potency active ingredients in development and production Micronization in development and production Strategic importance Contract manufacturing of new active ingredients

Senior Manager Laboratory Information Management System (LIMS) 23075 Senior Manager Laboratory Information Management System (LIMS) 23075 Company information Solvias is an internationally recognized provider of integrated solutions in contract analytical research, development and manufacturing. The company offers a broad spectrum of services and solutions in the Pharmaceutical, Biotech, Medical Device, Cell&Gene Therapy and Cosmetic industries. With headquarters near Basel, Switzerland, over 800 highly qualified employees take pride in putting science at the heart of serving customers to bring safer and better products to market faster. An exciting role in a dynamic professional environment - with plenty of possibilities for personal development and interaction with highly skilled and motivated colleagues. Your tasks Programming and Configuration: Develop and configure software solutions within the LIMS framework to meet specific global organizational needs. Collaborate with stakeholders to understand requirements and translate them into technical specifications. Implement enhancements and upgrades to improve LIMS functionality and performance. Conduct thorough testing, debugging, and troubleshooting of configurations and functionalities. Integration and System Support: Efficiently integrate LIMS with existing laboratory systems and workflows across multiple sites, ensuring smooth operation throughout the organization. Provide technical support and troubleshooting for LIMS-related issues. Ensure data integrity and system reliability through regular maintenance and monitoring. Lead technical discussions, provide expertise, and offer recommendations for enhancements and optimizations. Ensure the Global CORE template is protected and defined. Documentation and Compliance: Maintain accurate documentation of LIMS configurations, customizations, and processes. Ensure compliance with regulatory requirements such as FDA and ISO standards. Participate in validation activities to ensure LIMS meets regulatory and quality standards. Team and environment: As a senior member of our global team, you'll help to build and guide a talented group of LIMS professionals. You'll play a key role in offering guidance, mentorship, and opportunities for the growth the LIMS team members. Together, we'll cultivate a collaborative and innovative atmosphere where everyone can thrive. Stay up to date with emerging technologies, industry trends, and best practices in LIMS solutions. Challenge the status quo and provide solutions standard and efficient solutions. Requirements Bachelor's or Master's degree in Computer Science, Information Technology, or relevant experience in a similar role. Proficiency in programming languages such as LIMS Basic or other programming languages is a plus Knowledge of software development lifecycle (SDLC) and of computer systems validation (CSV). Experience with LIMS development and configuration. Experience with relational databases. Knowledge of laboratory processes, data management, and regulatory requirements. Strong problem-solving skills and attention to detail, with the ability to analyze requirements and propose solutions. Being able to communicate effectively with technical and non-technical stakeholders. Proven track record of successfully delivering global LIMS or IT projects on time and within budget. Our employees are very close to our hearts. At Solvias, you get: a well-structured onboarding program intensive training in the beginning the possibility for further development Furthermore, there are a multiple range of benefits like: flexible working time models 40 hours week at least 28.5 vacation days per year (depending on your age) commuter contribution for using public transport contribution to German and English language courses staff restaurant This job offer is a challenging opportunity in a company that values respect, responsibility, and reliability. At Solvias everyone counts and contributes to the success of the company. We strive to create an environment where we learn from each other and are open to feedback. Our employees are very close to our hearts. Each individual can make a difference and develop both professionally and personally. Does this appeal to you? We are looking forward to receiving your online application. Apply now SOLVIAS AG

Do you possess extensive experience as SAP Master Data Analyst? Are you someone who is motivated by challenges? Do you have a passion for analyzing data and understanding it? We are currently seeking a SAP Master Data Analyst for a leading pharmaceutical and diagnostic company in Switzerland.Tasks & Responsibilities:Coordinate with the local SAP development team for data export/importsPerform overall Master Data activities such as reporting, analysis, requirements gathering, etcJoin and/or complete Data Migration related workshops/trainingsPerform or ensure data cleansing tasks are completed on timeComplete data collection for manual/construction objects on timePerform and confirm value mapping performed by the Deployment Functional Data OwnersCreate and maintain master lists, if applicable, for assigned objectsProvide business insights and information to technical teams for extraction and conversion from the legacy system(s) for assigned data objectsEnsure data readiness and verify quality throughout the data journey for assigned data objectsVerify/validate that the data is fit for purpose (including alignment with internal/external stakeholders) and check upload files before and after load for all assigned data objectsPerform manual (type-in) data loads into target clients for assigned objects (if applicable)Perform dual maintenance and provide Data Migration Workbooks (DMWs) for delta load on time (if applicable)Act as SPoC for assigned objects as part of the defect management process during Hyper-careYour profile: Bachelor's and University Degree in Business, Computer Science, Finance, Accounting, Education, Engineering, Business/Administration, Management, Information Systems, Information Technology5+ years of experience in a similar role Experience with Materials and Production Master Data Tools and systems proficiency: SAP ERP (R3 & S4 HANA); SAP MDG-M, SAP DS/IS, SAP BW, BW/4HANA; SAP Analytics Cloud, Tableau or QlikView Excellent analytical mindset with the ability to communicate data-driven insights and recommendations to key stakeholdersStrong communication, and networking skills, someone who enjoys working with others and acts as a team playerStrong customer-centric, solution-oriented mindset with the ability to propose different solutions for the customers’ needsStrategic and holistic mindset with the ability to manage topics in agile / matrix organizationsFamiliar and comfortable with agile ways of working and adaptable to changing environmentsEnglish is a mustSkills with Excel Macros, Google Office (e.g. G-sheets a nice to have), database management We are looking forward to your application. Good luck.

Die Mitarbeitenden von STOBAG sind das Rückgrat unseres Unternehmens - gerade in Zeiten wie diesen. Als international tätiges Familienunternehmen gehört die STOBAG Gruppe mit über 700 Mitarbeitenden zu den Marktführern der Branche. Mit viel Eigenverantwortung und gutem Teamgeist arbeiten wir gemeinsam daran, unser in Design und Funktionalität überzeugendes Angebot ständig zu verbessern und auch international weiter zu wachsen. Unsere Kompetenzen liegen in der Entwicklung, der Produktion und im Vertrieb von innovativen Beschattungssystemen, Terrassendächern und Verglasungen. Gemeinsam ist es unser Ziel, Lebensräume wertvoller zu machen und dies über Generationen hinweg.Quality Manager 80 - 100% (m/w/d) DEINE AUFGABEN Digitalisierung im Quality Management standortübergreifend vereinheitlichen und vorantreiben Führen und Unterstützen der globalen Prozesseigner beim Erarbeiten von Prozessdokumentationen Leiten von internen und externen (SQS) ISO-Audits Entwickeln des aktuell bestehenden Quality Management hin zu einem Business Excellence Ansatz DEIN PROFIL technisches Grundstudium mit betriebswirtschaftlichem Verständnis Mehrjährige Erfahrung als Qualitätsmanager inkl. Prozessmanagement idealerweise im Industriesektor Kenntnisse von KVP Methodik und Business Excellence Modellen (z.B. EFQM) lösungsorientierter, selbständiger und verantwortungsbewusster Machertyp mit sehr guten Deutsch- und Englischkenntnissen DEINE PERSPEKTIVE Wir produzieren innovative und einzigartige Produkte, bei denen Technik und Design vereint werden. Eine Position, die dich in Bezug auf dein Fachwissen herausfordern wird, aber auch die Möglichkeit bietet, die eigenen Ideen einzubringen und selbständig zu handeln. Eine abwechslungsreiche, selbständige und verantwortungsvolle Herausforderung in einem Familienunternehmen, das langfristige Perspektiven eröffnet. Wir bieten dir ein spannendes Arbeitsumfeld in einem erfolgreichen Unternehmen. Du willst mehr über uns und unsere Anstellungsbedingungen erfahren? Du bist nur noch wenige Klicks entfernt - wir freuen uns auf deine Online-Bewerbung über unser Bewerbungstool.