7 Jobs für Six Sigma in Schweiz

For our client, one of the leading pharmaceutical companies, we are looking for a candidate with a degree in business informatics and experience managing procurement business processes. Additionally, you should have a good understanding of related business applications and be highly proficient in English.

General Information:
• Start date: ASAP
• Planned duration: 30.06.2026
• Extension: not likely
• Workplace: Rotkreuz or Basel
• Workload: 80-100%
• Remote/Home Office: Yes, max. 50% a week
• Team: ca. 14 people

Tasks & Responsibilities:
Business Process Management
• Responsible for the implementation of business processes and applications in alignment of the E2E Business Process Owner and other BPMs
• Responsible for holistic solution delivery including processes, technology, and analytics for own area, in line with the BPM strategy & guardrails and continuous improvement
• Responsible for global state-of-the-art process design/redesign within his/her business process area as part of the End-to-End process
• Mainly responsible for achieving lean processes and solutions, with maximum global standardization and harmonization for her/his responsible area

Business Process Governance
• Mainly responsible for the prioritization, justification, and realization of user stories/change requests according to stakeholder requirements
• Ensuring that process execution is robust and established as a way of working (e.g. by monitoring process compliance)
• Ensuring the documentation of the process requirements and the implementation through Standards and Guidelines

Project Management
• Leading and managing projects with manageable resource allocation, including planning, control, monitoring of activities, and providing technical guidance to small teams. This involves coordinating tasks and responsibilities among team members, ensuring the flow of information, and maintaining alignment with all relevant stakeholders.
• Responsible for achieving project goals and resolving issues within established guidelines and procedures, with oversight and direction from senior management. This includes regular updates on project status and preparation of necessary information.

Process Experts Support
• Ensuring continuous support of Process Experts and end Users (if required) with process problems and questions during and after the transfer
• Carry out problem analyses for sustainable elimination of the root cause

Must Haves:
• Degree (Bachelor) in business informatics, computer science or a related discipline (Business IT) 
• Minimum 3-5 years of professional experience in managing business processes in the area of Procurement, preferably within global Pharma or Medical Device manufacturing companies 
• Proven experience with Procurement (Source-to-Pay) processes and related applications. Good understanding of general business processes in associated areas (e.g. Finance, Supply Chain) 
• Personal initiative and a structured, independent, and solution-oriented way of working as well as the ability to keep a cool head in stressful situations and a high level of professional consulting skills
• High proficiency in English. Other languages such as German or Spanish will be desirable
• Experience from working cross-culturally in a global position
• Good understanding of related business applications (e.g. GEP SMART, SAP MM) 
• Ability to plan, organize, prioritize, work independently, and meet deadlines
• High willingness to take personal responsibility, can-do mentality
• Logical thinker, able to own, investigate, resolve problems, and incidents, resourceful and creative with the ability to work calmly and effectively
• Good project management expertise and knowledge of common project methods
• Excellent verbal and written communication, planning, analysis, and organization skills
• Very good team player as well as training and explanation skills

Your application

Please apply online. For further information about the position, please contact your Gi Group recruiter, Mrs. Anh Nguyen (+41 76 586 02 13).

About Gi Group

Gi Group is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world.

In Switzerland we operate with the brands Gi Group, Grafton, BauTech, Gi Life Sciences and former Kelly Services. We are active in temporary, permanent and professional staffing as well as in a variety of complementary HR Services. With a direct presence in 35 locations across Switzerland and over 250 employees, we are one of the leading staffing companies in the Swiss recruitment market.

Gi Group is specialist for Temporary and Permanent staffing and your valuable partner for many other HR Solutions. We are changing lives by connecting candidates with companies, and we work every day to create value. Your Job, Our Work.

Branche: Pharma-Industrie

Funktion: Technologie/EDV

Anstellungsart: Temporäre Arbeit

Our purpose is to empower organizations to transform the way they work by harnessing the full potential of artificial intelligence. We guide customers through the evolving digital landscape, enabling them to unlock new opportunities, enhance productivity, and deliver exceptional employee and customer experiences. By integrating advanced AI capabilities across devices, cloud platforms, and everyday business applications, we help organizations realize seamless, innovative, and secure solutions that drive sustained growth and success in the AI era.
At Small Medium Enterprises and Channel (SME&C), we are leading a high-growth, AI-powered global sales team-one that is deeply connected to our partners and driven by customer success. By uniting our Small Medium Business, Corporate, Strategy, and Partner teams, we are unlocking the largest customer opportunity, backed by the industry's most significant investments. Leveraging the power of AI and our extensive partner ecosystem, we are redefining how businesses of all sizes adopt technology to drive growth and innovation.
SME&C is more than a sales organization-it's a culture of innovation, opportunity, and inclusivity. Here, you'll be part of a diverse, high-performing, and customer-obsessed team where collaboration, connection, and continuous learning fuel everything we do.
If you thrive in a fast-paced, digital-first environment and are eager to make a meaningful impact, explore how SME&C DACH can be the next step in your career. Together, we are shaping the future of business.
Join Microsoft as an **AI Business Process Digital Solution Area Specialist.** In this individual-contributor, quota-carrying role you will own the entire engagement cycle, pinpointing opportunities, crafting value propositions, and driving AI-powered business-process transformations. Partnering closely with Account Executives, Digital Solution Engineers, and marketing teams, you will design win strategies, deliver compelling demos and pilots, and land customer success plans that accelerate adoption of Dynamics 365, Power Platform, and Copilot solutions.
Leveraging deep domain expertise and consultative selling skills, you will translate complex scenarios into clear business outcomes, remove blockers, and consistently meet or exceed revenue targets. You will also share best practices, expand your technical depth, and act as a trusted advisor who connects Microsoft innovation to measurable customer impact, advancing your own career growth in solution sales and cloud technologies.
Microsoft's mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond.
**Responsibilities**
+ Partner with and lead Account Planning Team on Account Plan for AI Business Process opportunities, including decision maker identification and solution play selection.
+ Establish and build C-Suite and Business Decision Maker (BDM) relationships as an industry aligned Business Applications solution expert.
+ Build & maintain the required range of qualified pipeline coverage for rolling 4 quarters through digital-first seller tools
+ Deliver the One Microsoft narrative and solution pitches to C-Suite executives and Business Decision Makers.
+ Orchestrate business value + technical solution demos to align with the customers' desired business outcomes and solution requirements.
+ Manage long-term contract renewals with existing accounts to ensure long-term satisfaction and successes.
+ Actively and regularly engage in sales community calls/channels and share learnings and best practices.
**Qualifications**
**Required Qualifications**
+ Demonstrated technology-related sales or account management experience
+ OR Bachelor's Degree in Computer Science, Information Technology, Business Administration, or related field AND technology-related sales or account management experience
+ OR equivalent experience
+ Full proficiency in French and English (both written and verbal)
+ German (Level C1 or higher) would be an advantage
**For Austria Only:** The salary for this role is starting from EURO 79,700 per annum depending on experience
#SMECCareers
Microsoft is an equal opportunity employer. Consistent with applicable law, all qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application process, read more about requesting accommodations ( .

Soziale Kanäle von medienjobs.ch

Anzeige vom: 15.08.2025

Adecco

Hai esperienza pregressa di almeno 5 anni in ambito Qualità - gestione tecnica dei fornitori, all'interno di realtà industriali di medie-grandi dimensioni?

Hai una formazione certificata sulle tecniche di audit e ottima conoscenza della lingua inglese?

Se sì, questa offerta potrebbe fare al caso tuo!

Responsabilità

• Gestione, sviluppo e controllo della qualità dei fornitori, e gestione delle Non Conformità

• Gestione tecnica dei fornitori (qualifiche, sviluppo, audit, gestione dei reclami e delle NC, monitoraggio delle azioni correttive e valutazione periodica)
• Gestione progetti di miglioramento nell'ambito della gestione fornitori
• Collaborazione nella verifica dei sistemi di gestione Q&A&S come auditore interno
• Collaborazione al mantenimento e al miglioramento dei sistemi di gestione Q&A&S

Il tuo profilo

• Laurea in ingegneria ad indirizzo tecnico, o scuola tecnica superiore

• Esperienza pregressa di almeno 5 anni in ambito Qualità - gestione tecnica dei fornitori, all'interno di realtà industriali di medie-grandi dimensioni
• Ottima conoscenza di norme ISO, sistemi di calibrazione, strumenti di misura
• Buona conoscenze della meccanica di precisione, e dell'elettrotecnica
• Preferibili conoscenze di tecnica della qualità, misurazione e statistica
• Formazione certificata sulle tecniche di audit
• Ottime competenze informatiche (SAP, Office)
• Ottima conoscenza della lingua inglese, la conoscenza di tedesco e/o francese costituirà un plus
• Disponibilità ed effettuare trasferte e visite ai fornitori
• Capacità di gestione progetti di miglioramento, di pianificazione, controllo, analisi e sintesi
• Propensione al lavoro in team e forti doti decisionali

Vantaggi

• Mensa

• Posto auto
• Medico aziendale
• Eventi per i dipendenti
• Formazione continua

Contatto

Interessato? Se le tue qualifiche ed esperienze corrispondono al profilo cercato, ti preghiamo di candidarti direttamente online

JN -072025-819704

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: CH0012138605) ed è quotato alla SIX Swiss Exchange (ADEN).



PERM
Technik und Fertigung

Branche: Anderes

Funktion: Anderes

Per azienda cliente, parte di un gruppo multinazionale e leader nella produzione e commercializzazione di macchinari ed interfacce per l'automazione industriale, siamo alla ricerca di un/una:

Lean Manufacturing specialist

OBIETTIVO

Il candidato si occuperà di  analizzare e ottimizzare i processi produttivi per ridurre gli sprechi e aumentare l'efficienza produttiva. A diretto riporto del Chief Operating Officer e in collaborazione con la Direzione, sarà responsabile dello sviluppo e attuazione di strategie lean volte al miglioramento del processo produttivo.

PEINCIPALI RESPONSABILITA'

• Implementare i principi e le metodologie della produzione snella

• Identificare le opportunità per migliorare l'efficienza e ridurre gli sprechi

• Formazione del personale sulle tecniche di produzione snella

• Condurre progetti di miglioramento continuo ed eventi Kaizen

• Condurre l'analisi delle cause principali per identificare e risolvere i problemi di produzione

• Monitoraggio e rendicontazione degli indicatori chiave di prestazione

• Conduzione di audit per garantire la conformità agli standard di lean

• Assistenza nella creazione di istruzioni di lavoro standardizzate

• Contribuire a risolvere qualsiasi problema o ostacolo che impedisca il processo di lean

REQUISITI PER LA POSIZIONE

• Esperienza comprovata come specialista di Lean Manufacturing o ruolo simile di almeno 10 anni

• Forte conoscenza dei principi e delle metodologie della produzione snella

• Ottime capacità di problem solving

• Forti capacità comunicative e interpersonali

• Capacità di formare e motivare il personale

• Laurea in ingegneria, preferibilmente gestionale

• Capacità di gestire efficacemente situazioni di stress

• Ottima conoscenza della lingua inglese

Completano il profilo ottime capacità organizzative, precisione e rispetto delle scadenze stabilite.

Branche: Elektronikindustrie/Automation

Funktion: Produktion

Anstellungsart: Festanstellung

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Finance
**Job Sub** **Function:**
Risk Management
**Job Category:**
People Leader
**All Job Posting Locations:**
Allschwil, Basel-Country, Switzerland, Schaffhausen, Switzerland
**Job Description:**
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s).
+ USA (Raritan, Titusville, New Brunswick, Horsham) Req #: R-029351
+ Belgium (Beerse) Req #: R-029481
+ Switzerland (Schaffhausen, Basel) Req #: R-029469
+ Ireland (Cork) Req #: R-029481
+ Netherlands (Leiden) Req #: R-029481
**Position Summary**
The Senior Director, Quality Risk Management & External Engagement has oversight for the Regulatory Intelligence Programs in Clinical and Commercial Manufacturing (GxP, GMP, cGMP), Risk Management and Proactive Quality Planning functions for Innovative Medicine Quality & Compliance. This position is critical to the strategic design and implementation of an effective and proactive Risk Management & Regulatory Intelligence framework to optimally prepare and support the Innovative Medicine Quality & Compliance organization while enabling proactive alignment with emerging industry trends.
**Key Responsibilities:**
+ Provide expert guidance on GxP compliance before, during, and after regulatory inspections, partnering with key stakeholders such as Regulatory Affairs and Compliance to facilitate effective communication with Health Authorities.
+ Conduct oversight activities across business units by applying risk-based methodologies to various risk types, including Health Authority Inspections, Audits, Compliance projects, and quality initiatives.
+ Oversee end-to-end risk management processes, ensuring comprehensive risk assessments, effective mitigation strategies, and continuous monitoring are implemented across the organization. Additionally, ensure that the organization possesses the necessary capabilities to conduct robust risk assessments.
+ Integrate the Enterprise Risk Management (ERM) Framework through Predictive Risk Monitoring efforts within the R&D Quality team, establishing foundational risk governance.
+ Collaborate effectively to facilitate the deployment of compliance improvement initiatives and programs, including tracking the performance of remediation efforts and addressing associated risks.
+ Coordinate independent confirmation and verification assessments, preparing a consolidated and actionable overview of risks related to remediation initiatives.
+ Build and lead a dedicated team that analyzes external industry trends and inspection outcomes to identify focus areas for improvement.
+ Actively monitor and evaluate external industry trends, regulatory developments, and best practices, using this information to inform strategic decision-making across the business.
+ Develop initiatives to integrate these insights into the Quality Management System (QMS) and operational procedures, ensuring alignment with industry standards and proactive risk mitigation.
+ Ensure that relevant information is proactively communicated to business partners and seamlessly integrated into audit and inspection readiness programs.
+ Identify and evaluate opportunities for process improvement based on compliance and risk monitoring outcomes.
+ Develop a comprehensive framework for evaluating key inputs while establishing an end-to-end governance process for assessing compliance and risk.
+ Reinforce the importance of compliance and quality within the organization, ensuring the effective implementation of compliance strategies and our ability to detect and quantify risk appropriately.
+ Serve as a key participant in industry forums and conferences to gain insights into emerging trends and developments within the industry, which will inform strategic initiatives and ensure that the organization remains aligned with best practices and competitive standards.
**Required Minimum Education** : BS degree required. Masters or advanced degree in a scientific field (Life Sciences, Pharmacy, Engineering) desirable.
**Required Years of Related Experience:**
+ Requires at least 15 years of experience with 5 plus years' experience and demonstrated leadership in a quality function working on complex and significant compliance topics.
+ Minimum 5 years of proven people leader experience
+ Must have comprehensive knowledge of GxP, GMP, cGMP and IT compliance regulations and guidelines, with expert knowledge on US and EMEA Regulations
+ Requires knowledge of latest auditing, investigation, and remediation techniques as well as leadership experience with inspections.
+ Demonstrated effective influencing, interpersonal, written, and verbal communications skills as well as a proven track record of sustaining compliance in complex organizations.
+ Regulatory Authority experience is desirable
+ Experience with Regulatory Authorities is a significant asset
**Required Knowledge, Skills and Abilities** :
+ Strong Quality and Compliance background with a deep understanding of Global GxP, GMP, cGMP requirements and the systems used to deploy them.
+ Experience in the identification and management of risks, including the development of risk-based remediation strategies and reporting risks/status in a concise manner.
+ Strong influencing and negotiation skills.
+ Excellent written and oral communication skills.
+ Strong interpersonal skills, including ability to communicate with individuals and groups at all levels. Experience establishing relationships with other functions within the company.
+ Strong decision making and analysis skills.
+ Demonstrated conflict and change management skills.
+ Strategic Thinking - ability to view bigger picture and translate complex issues into solution-based answers that drive real and sustainable change.
+ Proven hands-on experience with quality risk management methodologies
+ Strong computer skills with Quality Systems.
+ Sense of Urgency - ability to lead and deliver on multiple projects in a timely manner.
+ Teamwork and Collaboration - ability to lead, manage and participate on teams with shared responsibility for decisions and results.
+ Confidentiality - ability to maintain confidentiality as appropriate.
+ Systems Thinker - understanding how process / actions interact and influence other areas within a whole
**Required Years of Related Experience:**
+ Requires at least 15 years of experience with 5 plus years' experience and demonstrated leadership in a quality function working on complex and significant compliance topics.
+ Minimum 5 years of proven people leader experience
+ Must have comprehensive knowledge of GxP, GMP, cGMP and IT compliance regulations and guidelines, with expert knowledge on US and EMEA Regulations
+ Requires knowledge of latest auditing, investigation, and remediation techniques as well as leadership experience with inspections.
+ Demonstrated effective influencing, interpersonal, written, and verbal communications skills as well as a proven track record of sustaining compliance in complex organizations.
+ Regulatory Authority experience is desirable
+ Experience with Regulatory Authorities is a significant asset
**Required Knowledge, Skills and Abilities** :
+ Strong Quality and Compliance background with a deep understanding of Global GxP, GMP, cGMP requirements and the systems used to deploy them.
+ Experience in the identification and management of risks, including the development of risk-based remediation strategies and reporting risks/status in a concise manner.
+ Strong influencing and negotiation skills.
+ Excellent written and oral communication skills.
+ Strong interpersonal skills, including ability to communicate with individuals and groups at all levels. Experience establishing relationships with other functions within the company.
+ Strong decision making and analysis skills.
+ Demonstrated conflict and change management skills.
+ Strategic Thinking - ability to view bigger picture and translate complex issues into solution-based answers that drive real and sustainable change.
+ Proven hands-on experience with quality risk management methodologies
+ Strong computer skills with Quality Systems.
+ Sense of Urgency - ability to lead and deliver on multiple projects in a timely manner.
+ Teamwork and Collaboration - ability to lead, manage and participate on teams with shared responsibility for decisions and results.
+ Confidentiality - ability to maintain confidentiality as appropriate.
+ Systems Thinker - understanding how process / actions interact and influence other areas within a whole.
+ Travel requirements: approximately 20-30% global travel will be required.
This position is located in the US or EU and can be based at any Innovative Medicine Supply Chain site.