52 Jobs für Sap Qm in Schweiz

Join Accelleron and work in a team that is dedicated to creating a future where innovative digital technologies allow greater access to cleaner energy.  Accelleron is at the helm of the global industry in the manufacture and maintenance of turbochargers for 500 k W to 80+ MW diesel and gas engines. Our leading-edge technology and innovation enable our customers to perform better and produce fewer emissions, even in the toughest terrains. Approximately Accelleron turbochargers are in operation across the globe on ships, power stations, gen-sets, diesel locomotives and large, off-highway vehicles. About the Position:With production sites and subsidiaries in 50 countries, this position has a global scope. Reporting to the Head of IS Production & Value Chain in Switzerland, you'll join a skilled IT team to plan, design, implement, maintain, and improve IT processes for global quality management. The role involves consulting, planning and executing the transition from the current application landscape to the future system landscape in alignment with transformation projects. Effective communication skills are required to understand the requirements of internal customers, particularly within the Production and Supply Chain organization and to develop these needs within global Quality Management processes. Are you exceptionally committed, a self-starter with strong interpersonal skills and the ability to apply logical thinking? Then we are looking forward to meeting you! Your Responsibilities: Application Owner SAP QM: As the SAP QM Application Owner, you serve as the primary contact for production, procurement and logistics departmentregarding SAP QM across ECC, S/4 HANA Public Cloud, and EWM systems. You ensure seamless integration with related SAP modules such as PP, MM and decentralized EWM and lead SAP QM aspects of the S/4 HANA Private Edition Migration project. Your role includes advising departments on SAP QM, supporting process optimization with business power users, and coordinating application strategy and implementation with Divisions, Functions and Group IS delivery. Tasks: Collaboration in ongoing projects for the rollout of SAP QM in our Plants in Switzerland and China Planning and implementation of projects for the rollout of SAP QM at the production plant in Baden, Switzerland Represent the Divisions and Functions interests in IS projects in the role as application owner and process engineer for assigned quality management applications and processes Ensure smooth operation of all applications and modules in your area of responsibility Ensure high quality of data in close cooperation with powerusers and end users to optimize business value Strengthening the business organization including the poweruser in the areas of Quality ManagementAssist in testing, documentation and end user training Process Engineer Quality Management: As a Process Engineer in Quality Management, you analyze and optimize quality management processes for the global Turbocharging Business. You identify improvement opportunities through new technologies or applications, working closely with the business to evaluate these options transparently. In related projects, you serve as both a project member and main IT contact. You also track trends and digitalization technologies to enhance Accelleron's process efficiency. Tasks: Definition of application strategy, roadmapand implementation together with the Application Owner Role in close cooperation with needed colleagues, third party suppliers, Division, Functionand IT delivery functions Consulting of the business during implementation of process optimization within IT applications Project management on workstream level and participation in process improvement projects Build up and extend knowledge about Divisions and Functions business processes and application landscape Continuous analysis, enhancement and optimization of quality management processes within the Global Accelleron organization in close collaboration with your business counterparts Ensure structured and transparent evaluation of new applications / modules / functions Identify trends and key enabling technologies around digitalization to contribute to the increase of division process efficiency or value creation with new business models Providing leadership to temporary work teams and externals, guiding and monitoring task completion, disseminating expert knowledge and advice Your Background: Formal Education & Certification: University degree or college diploma in computer science or equivalent work experienceProficiency in English and German is essentialKnowledge & Experience: Minimum of 5 years of experience as a functionalconsultant or similar roles in SAP QM in industry with strong focus on production, supply chain and warehouse management A background in quality management, logistics, procurement, computer scienceor similar field optimally in discrete manufacturing industriesExperience with S/4 HANA private and public cloud edition Experience with SAP QM, PP, MM and QM integration to decentralized EWMExperience with SAP integration / interface projects and technologies like CPI, Idoc,etc. is a plus Personal Attributes: A high level of self-motivation, curiosity and hands-on mentality The ability to manage multiple demands on time, working with cross-functional, virtual, and international teams Identification and removal of obstacles/escalation and cross-functional conflict resolution A collaborative, solutions- and customer service-oriented approach Your benefits:CanteenChildcareModern office, smart workingFlexible working modelAttractive holiday planRemote work policyEmployee assistance programWe look forward to receiving your application. If you want to discover more about Accelleron, take another look at our website . Accelleron Data Privacy Statement: jid8fc12ebje jit0938je jiy25je

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
**We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.**
We are searching for a QA SPECIALIST.
**What your responsibilities will be**
+ You will ensure that manufacturing practices and operations comply with internal and external regulations, with a special focus on Change Control processes.
+ You will initiate and follow up on Change Controls, perform risk and impact assessments, and coordinate implementation and documentation.
+ You will lead internal Change Control meetings and collaborate with all involved stakeholders.
+ You will manage failure investigations, perform root cause analysis, and initiate appropriate CAPAs.
+ You will support the preparation of Management Reviews and the technical market release process.
**Who you are**
+ You have a university degree in a scientific or technical field.
+ You have experience in Quality Assurance within a GMP-regulated environment.
+ You are familiar with risk assessment methodologies, Change Control processes and QMS tools.
+ You have strong analytical, organizational, and communication skills.
+ You are fluent in English; knowledge of German and/or French is a plus.
+ You are a team player with a systematic and proactive approach.
**What we offer**
It's a brilliant opportunity for someone with the right talents.
You'll join a collaborative and innovative team committed to quality and continuous improvement.
We offer professional development opportunities and a chance to contribute to life-saving diagnostic products.
**Contract of Employment:** Permanent position
**Flexibility for U Program:** 1 day remote working possible
#LI-HJ1
**Location: EMEA : Switzerland : Düdingen:Suiza**
Learn more about Grifols ( ID:**
**Type:** Regular Full-Time
**Job Category:**

For our client's company in Basel, we are looking for a

Quality Assurance Manager

• You review and approve SOP's, protocols, reports, Certificate of Analysis and other quality-related documents
• You have a high sense of detail orientation and support investigations of deviations and out of specifications (OOS)
• You maintain, record and process corrective and preventive measures (CAPA's)
• You act as a Quality Assurance point of contact for our customers
• You have a high level of customer orientation and you organize and manage customer audits and inspections
• You apply and interpret audit and compliance requirements
• You perform internal audits and provide support for GMP training

Requirements

• You have a scientific education (Master degree) in analytical chemistry, biochemistry or life sciences
• You are fluent in English and German
• You worked for at least 7 years in the analytical-pharmaceutical environment having preferably proven experience in Quality Assurance
• You have profound expertise in the regulatory framework in the GMP environment such as ICH, FDA, USAP, Ph. Eur.
• You have a background in data integrity and computerized systems, risk assessment and project support
• You convince us with your problem-solving skills and outstanding communication skills to collaborate with your future team-members and various stakeholders
• If you have gained experience as an auditor, then this is an asset

Branche: Pharma-Industrie

Funktion: Qualitätsprüfung

Anstellungsart: Festanstellung

Karrierestufe: Management

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
**Join Thermo Fisher Scientific Inc. for an exceptionally rewarding career where your contributions help craft the future of science and health!**
**Job Description**
As an engineer at Thermo Fisher Scientific Inc., you will be at the forefront of innovation and excellence in the pharmaceutical industry. Your work will be crucial in ensuring the flawless execution of our manufacturing processes and the successful implementation of quality and compliance measures.
**Responsibilities:**
+ Ensure compliance of the manufacturing processes, batch record, deviation, change control, and CAPA.
+ Review and approve completed batch records within defined timelines.
+ Responsible for technical batch release.
+ Provide active on-the-floor support to the production team.
+ Review and approve operational elements such as procedures and related documents, including specifications, working instructions, and impact assessments.
+ Assist with continuous improvement initiatives related to quality documents and processes.
+ Supervise the preparation of the Annual Product Review (APQR) and ensure its execution within the due date.
+ Be present on the floor during critical manufacturing steps.
+ Uphold and share data integrity rules (ALCOA+).
+ Propose improvements to flows, manufacturing activities, and organizational processes.
**Qualifications:**
+ Seeking pharmacists or scientists with a master's degree or equivalent experience. Requires 3-5 years in pharma (biotech) and 1 year in commercial batch release.
+ In-depth knowledge of pharmaceutical manufacturing processes, particularly biologic drug substances.
+ Proficient in German and English, with strong oral and written communication skills.
+ Experience with SAP and electronic MES (manufacturing execution system) is a plus.
+ Ability to provide on-call services remotely based on departmental needs.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Thoratec Switzerland GmbH** is part of the medical device division of **Abbott Laboratories** , a fortune 500 company with over 115'000 employees worldwide. We are the global market leader for implantable and extracorporeal blood pumps based on magnetic levitation technology. Our life-saving systems, which we develop and manufacture in Zurich, are used for advanced heart failure patients needing short- or long-term circulatory support.
Our location in the heart of the city of Zurich has around 130 employees in the areas of development, quality and production of the **CentriMag** system and the **HeartMate 3.**
Are you a strategic leader passionate about quality, innovation, and making a difference in healthcare? Join our Zurich team as **Senior Manager Quality Assurance** , where you'll lead with purpose, foster collaboration, and shape the future of our quality systems in a dynamic and inclusive environment.
**Position Overview**
As the **Senior** **Quality Manager Quality Assurance** for our Zurich site, you'll be the key point of contact for all quality-related matters, including interactions with external regulators and Notified Bodies. You'll lead the development and execution of our site's Quality strategy, ensuring alignment with global standards and business goals, while championing continuous improvement and operational excellence.
This role offers a unique opportunity to influence site-wide strategy, guide cross-functional teams, and support the expansion of manufacturing capabilities, including clean room processes. You'll work closely with senior leadership and empower a talented team to deliver high-quality, safe, and compliant products that improve lives.
**Key Responsibilities**
**Compliance & Regulatory Leadership**
+ Serve as the Quality Management Representative for the Zurich site and manufacturer of the Centrimag product line.
+ Ensure compliance with global quality system regulations (USA, EU, Korea, Brazil, Australia, Canada, Ukraine, Switzerland).
+ Lead site readiness for inspections and audits, and represent the facility during regulatory and internal audits.
**Team Leadership & Development**
+ Lead and mentor a diverse team across operations quality, regulatory compliance, supplier quality, and new product development.
+ Foster a culture of inclusion, collaboration, and continuous learning.
+ Identify and manage resource needs to support operational excellence and future growth.
**Quality Systems & Process Excellence**
+ Oversee quality system processes including document control, CAPA, risk management, supplier evaluations, and complaint handling.
+ Support centralized functions like Regulatory Affairs and vigilance reporting with timely and accurate data.
+ Drive improvements through data analysis and quality management reviews.
**Product Acceptance & Customer Safety**
+ Own final decisions on product quality and release, ensuring compliance and customer protection.
+ Manage non-conformance evaluations and ensure timely resolution aligned with patient safety.
**Strategic Planning & Budget Management**
+ Plan and manage the Quality department budget in alignment with business objectives.
+ Collaborate with Finance, Site Director, and divisional leadership to ensure responsible and strategic resource allocation.
**Cross-Functional Collaboration**
+ Partner with Operations, R&D, and external stakeholders to resolve quality issues and support product development.
+ Contribute to Zurich site strategy and support the integration of new manufacturing processes.
**Qualifications - What Will Help You Thrive in This Role**
+ A **Master's degree** in Science, Engineering, or a related technical field, with **10+ years of experience** in the medical device industry.
+ At least **5 years of leadership experience** in a quality systems environment, ideally within medical devices.
+ Strong understanding of **ISO standards** and global regulatory frameworks (e.g., US, EU) related to medical devices.
+ Proven ability to **lead and inspire teams** , with a focus on coaching, development, and inclusive leadership.
+ Comfortable using business and technical software tools; open to learning new systems.
+ Strong analytical and decision-making skills, with a collaborative and solution-oriented mindset.
+ Excellent communication skills in English, with German proficiency considered an asset for engaging a broad range of stakeholders.
+ Able to work independently and collaboratively across **global teams** , including remote sites.
+ Highly organized, with strong time management and prioritization abilities.
+ Skilled in building relationships and navigating complex environments with empathy and professionalism.
+ Committed to ethical standards and delivering high-quality outcomes.
**Working at Abbott**
At Abbott, you can do work that matters and help people to live a healthier and fuller life, grow your career, and learn, be your true self. You will have access to:
+ Career development with an international company where you can grow
+ A workplace in a fortune 500 company and the world's leading manufacturer of medical devices
+ A challenging position in a crisis independent industry
+ To become part of a dynamic, highly educated, highly skilled, and motivated team
+ Multi-national environment, where we foster the development of our talents within the enterprise
+ Competitive compensations and benefits
+ A workplace in the heart of Zurich
Please follow our Career site and check for available openings:
Abbott Jobs | Apply Now | Abbott Laboratories Careers ( Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Adecco

Hai un background accademico in ingegneria meccanica, elettrica o industriale? Sei fluente in italiano ed inglese? Stai cercando una sfida stimolante all'interno di un contesto aziendale dinamico?

Se hai risposto affermativamente, allora questo annuncio potrebbe interessarti.

Responsabilità

Responsabilità:

Sarai responsabile della gestione e supervisione di tutte le attività di assicurazione qualità lungo l'intero ciclo di vita degli strumenti e dispositivi meccanici ed elettromeccanici. Dalle revisioni iniziali del design alla produzione e ai test finali, garantirai che i prodotti rispettino costantemente i più alti standard di qualità e le aspettative dei clienti.

Collaborerai strettamente con team interfunzionali?tra cui ingegneria, approvvigionamento e produzione?oltre che con clienti e fornitori, mettendo a frutto la tua esperienza su componenti meccanici ed elettrici per assicurare prestazioni, conformità normativa e piena tracciabilità del prodotto.

• Supervisionare delle attività QA lungo l'intero ciclo di vita del prodotto
• Sviluppo e implementazione di piani e procedure di qualità in linea con la normativa ISO 9001 e i requisiti specifici dei clienti
• Revisione e approvazione della documentazione tecnica, della selezione dei componenti e della qualifica dei fornitori
• Collaborazione con i differenti team interni per definire e implementare strategie di controllo qualità per componenti meccanici ed elettrici
• Partecipazione attiva ad ispezioni, revisioni interne e test di accettazione da parte dei clienti
• Gestione di non conformità e deviazioni, conduzione root causes analysis e implementazione di azioni correttive in collaborazione con gli ingegneri R&D
• Gestione della qualità dei fornitori attraverso onboarding, audit e verifica della conformità
• Supporto all'introduzione di nuovi prodotti (NPI) definendo i requisiti QA e contribuendo ai processi di validazione e rilascio
• Mantenimento e miglioramento del Sistema di Gestione Qualità (QMS), supportando gli audit ISO 9001 e contribuendo alle iniziative di miglioramento continuo
• Responsabilità della piena tracciabilità dei documenti di qualità, inclusi risultati di ispezione, certificazioni dei fornitori e documentazione delle modifiche

Il tuo profilo

• Formazione accademica in Ingegneria Meccanica, Elettrica o Industriale
• Esperienza pregressa (3-5 anni) in ambito QA di prodotto (ingegneria meccanica o produzione elettromeccanica)
• Solida conoscenza del quadro normativo ISO 9001
• Competenze nella pianificazione della qualità, audit e gestione fornitori
• Esperienza con componenti meccanici ed elettrici
• Capacità di lettura del disegno tecnico, applicazione e verifica delle tolleranze, utilizzo di strumenti di misura
• Ottima conoscenza dell'italiano e dell'inglese
• La conoscenza del tedesco e del francese costituisce un plus
• Mentalità strutturata, attenzione ai dettagli e forte curiosità professionale

Vantaggi

Contratto di lavoro a tempo indeterminato all'interno di un'azienda di piccole dimensioni, solida e dinamica.

Contatto

Se il tuo profilo corrisponde a quanto stiamo ricercando, non esitare a trasmettere la tua candidatura attraverso il nostro sito web

(riferimento: JN - )

Chi siamo

Adecco è leader di mercato per le soluzioni di staffing in Svizzera e nel mondo. Ogni giorno, i nostri team nelle nostre circa 50 sedi in tutta la Svizzera assicurano il miglior incontro tra candidati e clienti in diversi ambiti professionali e settori. Il Adecco Svizzera è una società del Gruppo Adecco, leader a livello globale per Talent Advisory e Solutions. Siamo profondamente convinti di poter far sì che tutti siano in forma per il futuro e impieghiamo più di 3,5 milioni di persone quotidianamente. Reclutiamo, sviluppiamo e creiamo talenti in 60 Paesi, permettendo alle organizzazioni di contribuire a plasmare il futuro del lavoro. In quanto società Fortune Global 500, fungiamo da esempio, generando un valore condiviso che stimola l'economia e contribuisce a una società migliore. Il Gruppo Adecco ha la sua sede principale a Zurigo, in Svizzera, (ISIN: CH ) ed è quotato alla SIX Swiss Exchange (ADEN).



PERM
Technik und Fertigung

Branche: Anderes

Funktion: Anderes

Fly with us into the future and become part of the team at one of the most innovative aircraft manufacturers in the world.

Your Tasks

Technical, disciplinary, and personnel leadership of the Quality Assurance department with approximately 25 employees

Budget and cost responsibility for your own cost center

Responsibility for quality assurance of the assembly line

Performing the role of Safety Officer and Certifying Staff for Permit to Fly in the aircraft assembly area

Continuous development of the business area and reporting directly to the VP Assembly & MRO

With this you convince us

Basic technical training with further education at HF level or similar

Solid experience and expertise in aviation, particularly in the area of EASA/FAA Part 21

Distinct leadership experience at Director's level

Very good technical expertise in the aircraft assembly area

Very good written and spoken German and English

Efficient and effective working style, able to work independently on a variety of topics with the right priorities

Above-average motivation in a dynamic, growing environment

What we offer

A committed, international team and unique projects 

Flexible working hours and individual pension solutions 

Support for training and opportunities for personal and professional development 

Discounted meals in our staff restaurant and various discounts for employees 

Team events at which we celebrate our successes together 

Are you a strategic leader passionate about quality, innovation, and making a difference in healthcare? Join our Zurich team as Senior Manager Quality Assurance, where you’ll lead with purpose, foster collaboration, and shape the future of our quality systems in a dynamic and inclusive environment.Position OverviewAs the Senior Quality Manager Quality Assurance for our Zurich site, you’ll be the key point of contact for all quality-related matters, including interactions with external regulators and Notified Bodies. You’ll lead the development and execution of our site’s Quality strategy, ensuring alignment with global standards and business goals, while championing continuous improvement and operational excellence.This role offers a unique opportunity to influence site-wide strategy, guide cross-functional teams, and support the expansion of manufacturing capabilities, including clean room processes. You’ll work closely with senior leadership and empower a talented team to deliver high-quality, safe, and compliant products that improve lives.Key ResponsibilitiesCompliance & Regulatory LeadershipServe as the Quality Management Representative for the Zurich site and manufacturer of the Centrimag product line.Ensure compliance with global quality system regulations (USA, EU, Korea, Brazil, Australia, Canada, Ukraine, Switzerland).Lead site readiness for inspections and audits, and represent the facility during regulatory and internal audits.Team Leadership & DevelopmentLead and mentor a diverse team across operations quality, regulatory compliance, supplier quality, and new product development.Foster a culture of inclusion, collaboration, and continuous learning.Identify and manage resource needs to support operational excellence and future growth.Quality Systems & Process ExcellenceOversee quality system processes including document control, CAPA, risk management, supplier evaluations, and complaint handling.Support centralized functions like Regulatory Affairs and vigilance reporting with timely and accurate data.Drive improvements through data analysis and quality management reviews.Product Acceptance & Customer SafetyOwn final decisions on product quality and release, ensuring compliance and customer protection.Manage non-conformance evaluations and ensure timely resolution aligned with patient safety.Strategic Planning & Budget ManagementPlan and manage the Quality department budget in alignment with business objectives.Collaborate with Finance, Site Director, and divisional leadership to ensure responsible and strategic resource allocation.Cross-Functional CollaborationPartner with Operations, R&D, and external stakeholders to resolve quality issues and support product development.Contribute to Zurich site strategy and support the integration of new manufacturing processes.Qualifications – What Will Help You Thrive in This RoleA Master’s degree in Science, Engineering, or a related technical field, with 10+ years of experience in the medical device industry.At least 5 years of leadership experience in a quality systems environment, ideally within medical devices.Strong understanding of ISO standards and global regulatory frameworks (e.g., US, EU) related to medical devices.Proven ability to lead and inspire teams, with a focus on coaching, development, and inclusive leadership.Comfortable using business and technical software tools; open to learning new systems.Strong analytical and decision-making skills, with a collaborative and solution-oriented mindset.Excellent communication skills in English, with German proficiency considered an asset for engaging a broad range of stakeholders.Able to work independently and collaboratively across global teams, including remote sites.Highly organized, with strong time management and prioritization abilities.Skilled in building relationships and navigating complex environments with empathy and professionalism.Committed to ethical standards and delivering high-quality outcomes.Working at Abbott At Abbott, you can do work that matters and help people to live a healthier and fuller life, grow your career, and learn, be your true self. You will have access to: Career development with an international company where you can grow A workplace in a fortune 500 company and the world’s leading manufacturer of medical devices A challenging position in a crisis independent industry To become part of a dynamic, highly educated, highly skilled, and motivated team Multi-national environment, where we foster the development of our talents within the enterprise Competitive compensations and benefits A workplace in the heart of Zurich Please follow our Career site and check for available openings:  Abbott Jobs | Apply Now | Abbott Laboratories Careers   jidc99c190je jit0938je jiy25je

Why should you apply?Real-world projects with impact: you will collaborate with like-minded peers and tackle challenging projects, developing cutting-edge technology solutions, learning on the job since day oneProfessional development and training: you will enhance your technical and soft skills through dedicated learning & development initiativesMentorship by industry leaders: you will gain invaluable insights from seasoned professionals who have successfully paved their paths in the engineering landscapeNetworking opportunities: you will forge lifelong connections with fellow engineers and industry experts, enabling you to establish meaningful relationships that will propel your career forwardRecognition and reward: your contribution will be recognized. Coesia Graduates Program rewards those who consistently strive for excellence.About the RoleJoin Hapa AG as a Quality Assurance Engineer (m/f/d) and play a key role in ensuring the quality and reliability of our production processes, with a specific focus on machinery and printing machinesResponsibilitiesCollaborate closely with Production, Procurement, Quality, and HSE Managers to ensure the quality and reliability of production processes, emphasizing machinery and printing machinesEnsure effective handling and resolution of non-conformities in production, including deviation openingMonitor and analyze quality performance metrics, identifying process improvement opportunities with the team to ensure high production qualityManage complaints if requiredWork closely with Manufacturing, Engineering, Procurement, Technical Support, and Suppliers to develop and implement robust manufacturing processes and quality controlsEnsure compliance with ISOrequirements within the production environmentManage and coordinate CAPA (Corrective and Preventive Actions) processes, as well as Production Deviation management, ensuring timely resolution and continuous improvementCoordinate with suppliers to address quality-related issues promptly and effectivelySupport Factory Acceptance Testing processes and lead quality actions to ensure adherence to quality standards What You Need to Be SuccessfulMaster’s degree in Engineering, Quality Management, or related field0-18 months experience in Quality Production Management within a manufacturing environment (internships included)Fluency in English & GermanStrong team player with excellent interpersonal and communication skillsPositive attitude and proactive approach to problem-solving Additional AssetsKnowledge of ISO 9001:2015 standard and quality management principlesExperience in managing CAPAs, production deviations, and supplier deviationsExperience in a GMP environmentFamiliarity with the Machinery Directive (2006/42/EC) and experience with printing inksIf this sounds like a role that matches your passion and skills, we look forward to your application!Kindly note that due to GDPR we will not accept applications via mail. Please use the link to apply via our career site. External agencies are kindly requested not to contact the company regarding this position.If you have any questions, feel free to reach out to Siri Taripanah at Coesia is an equal-opportunity employer and embraces diversity and inclusion. jid913dbf0je jit0938je jiy25je