KI-Beschreibung

In dieser Rolle übernimmst du die Leitung eines Personalrestaurants in St. Niklaus VS, führst ein engagiertes Team und sorgst für den nachhaltigen Erfolg des Betriebs. Dein Alltag umfasst sowohl administrative Aufgaben als auch die aktive Mitgestaltung der Geschäftstätigkeit sowie die Organisation von besonderen Anlässen.

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  Mindestens 5 Jahre Erfahrung in vergleichbarer Funktion in Gastronomiebetrieb
• •
  Abgeschlossene Lehre als Koch EFZ
• •
  Solide Kenntnisse in Kalkulations- und Warenbewirtschaftungssystemen

Deine Vorteile

KI-Beschreibung

Dein Alltag besteht darin, internationale Gäste auf höchstem Niveau professionell zu betreuen. Du koordinierst die Abläufe in deinem Bereich und sorgst mit einem Lächeln für einen erstklassigen Service.

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  Gute Deutsch-, Französisch- und Englischkenntnisse
• •
  Fundierte Weinkenntnisse
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  Ein paar Jahre Erfahrung in gehobener Gastronomie

Deine Vorteile

KI-Beschreibung

In this role, you will play a crucial part in ensuring that API production meets GMP standards. Your day-to-day responsibilities will involve collaborating with various teams, managing documentation, and serving as the quality liaison during client audits.

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  University degree in Life Sciences
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  First experience in GMP environment, preferably in biopharmaceutical industry
• •
  Fluency in English and German (written and verbal)

Deine Vorteile

KI-Beschreibung

As a Senior QA Specialist in Process Validation, you will oversee the validation of manufacturing processes in biopharmaceutical plants, ensuring compliance and quality throughout the product lifecycle while collaborating with various teams.

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  Master's degree or PhD in Chemistry, Biotechnology, or related field
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  Significant experience in biopharmaceutical manufacturing, preferably in validation
• •
  Broad knowledge of manufacturing processes in GMP environment

Deine Vorteile

KI-Beschreibung

In this role, you will play a crucial part in ensuring compliance by supporting validation specialists and reviewing key documents. Your day-to-day responsibilities will involve collaborating with development teams and participating in audits, all while enhancing validation procedures.

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  Master's degree or PhD in Chemistry, Biotechnology, or related field
• •
  Significant experience in biopharmaceutical manufacturing, preferably in validation
• •
  Broad knowledge of manufacturing processes in GMP environment

Deine Vorteile

KI-Beschreibung

In this role, you will focus on ensuring product quality by completing necessary training, supporting compliance efforts, and actively participating in validation processes. Your day-to-day responsibilities will include preparing newsletters, maintaining status overviews, and serving as a key contact during audits.

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  Academic degree in Chemistry, Biotechnology, or related field
• •
  Fluency in English and German
• •
  Experience in GMP manufacturing

Deine Vorteile

KI-Beschreibung

As a Senior Quality Excellence Manager, you will drive operational excellence and foster a LEAN culture within the Quality organization, ensuring process standardization and supporting project teams in achieving their goals.

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  University Degree in a scientific area or absolved apprenticeship in a pharmaceutical environment
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  Profound experience in a GMP regulated environment
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  Experience with Lean /
  Six Sigma in a Quality related environment

Deine Vorteile

KI-Beschreibung

In this role, you will manage quality assurance projects while ensuring API production meets GMP standards. You will collaborate with various teams, oversee documentation, and support continuous improvement initiatives, serving as the key quality contact during client audits.

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  Academic degree in Life Sciences, Microbiology, Biotechnology, Chemistry, or related field
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  Significant experience in the biopharmaceutical industry in a GMP environment
• •
  Strong communication skills and regulatory awareness with a proactive, team-oriented mindset

Deine Vorteile

KI-Beschreibung

In dieser Rolle koordinierst du die Produktionsprozesse und bist die Ansprechperson für technische Störungen. Du leitest ein Team, optimierst Abläufe und sorgst dafür, dass alle Aktivitäten den cGMP-Richtlinien entsprechen.

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  Lehrabschluss als Chemie-Pharmatechnologe EFZ oder vergleichbar
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  Mehrjährige Berufserfahrung in der GMP Produktion von API oder Biologics
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  Erfahrung in der Beschaffung und Qualifizierung von Equipment unter GMP

KI-Beschreibung

In this role, you will oversee the management of deviations and CAPA processes in logistics and hygiene, ensuring compliance with GMP standards while driving continuous improvement initiatives across production sites.

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  Minimum of 5 years of experience in GMP-regulated biopharmaceutical or manufacturing environment
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  Bachelor’s or Master’s degree in Logistics Engineering, Engineering, Material Management, Hygiene, or related field
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  Strong knowledge of deviation management and CAPA processes

KI-Beschreibung

In this role, you will play a vital part in production operations, supporting the team during busy periods and complex processes. Your expertise will help ensure smooth operations while also providing training and assistance to fellow team members.

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  Solid technical knowledge and expertise in production operations and equipment handling
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  Proficiency in English
• •
  Strong team player with excellent collaboration skills

Deine Vorteile

KI-Beschreibung

As a Project Manager in Process Development Logistics, you will lead dedicated programs from inception to implementation, collaborating with senior stakeholders and project teams to drive improvements and ensure successful outcomes across departments.

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  Minimum of 5-6 years in Supply Chain/
  Operations role with leadership experience in pharmaceutical or regulated industry
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  Master's degree in Business Administration, Life Sciences, Engineering, Logistics, or related field, or equivalent experience
• •
  Lean Management Certification

Deine Vorteile

KI-Beschreibung

In dieser Rolle als QC Senior Lab Technician bist du für die Durchführung wichtiger mikrobiologischer Analysen verantwortlich. Dein Alltag umfasst die Planung und Dokumentation von Methodenverifizierungen sowie die Gewährleistung der Sauberkeit im Labor.

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  Abgeschlossene Ausbildung als Biologielaborant, BTA, BSc Biologie oder vergleichbar
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  Erfahrung im GMP-Umfeld von Vorteil
• •
  Erfahrung mit mikrobiologischen Untersuchungen von Vorteil

Deine Vorteile

KI-Beschreibung

As the Head of Shift for Buffer Prep, you will lead a dynamic team in producing buffers for various platforms. The role focuses on staff development, training, and ensuring compliance with industry standards while optimizing production efficiency.

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  At least 5-10 years relevant hands-on experience in GMP production area in pharma or regulated fields
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  Berufsabschluss EFZ (CPT oder BICO/
  CHEMCO) BS /
  MS in Chemistry, Biotechnology
• •
  Fluency in German and English (at least level B1-B2)

Deine Vorteile

KI-Beschreibung

In this role, you will oversee operational activities in Downstream Processing, guiding a team to ensure the efficient manufacturing of therapeutic proteins while maintaining compliance with safety standards. Your daily responsibilities will include planning, training, and leading optimization projects.

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  Significant work experience (>5 years) in Downstream Processing in biotech/
  biopharma industry
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  In-depth knowledge of downstream processing techniques
• •
  Excellent GMP understanding

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of quality assurance, managing customer and internal audits while ensuring compliance during regulatory inspections. Your day-to-day responsibilities will involve planning audits, coordinating with teams, and presenting quality systems to clients.

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  Academic degree in Chemistry, Biotechnology, or Life Sciences
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  Fluency in English and German
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  General knowledge of manufacturing processes and analytical methods

Deine Vorteile

KI-Beschreibung

In this role, you will take charge of quality management for API manufacturing, ensuring compliance with cGMP standards while acting as the key contact for quality-related inquiries. Your day-to-day responsibilities will involve overseeing audits, providing guidance, and making critical quality decisions.

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  Academic degree in Life Science, Chemistry, Biotechnology, or related field
• •
  Experience in GMP regulated pharmaceutical or API industry
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  Ability to identify non-compliance and gaps from quality standards

Deine Vorteile

KI-Beschreibung

In dieser Rolle übernimmst du die fachliche und personelle Führung eines 2-Schicht-Teams im Bereich Flüssiggase. Du organisierst den Schichtbetrieb, förderst die Weiterentwicklung des Teams und bist die Ansprechperson für externe Stellen im Ereignisfall.

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  Mehrjährige Erfahrung (5–10 Jahre) als stellvertretende/
  r Schichtführer/
  in oder Anlagespezialist/
  in in der chemischen Produktion oder verwandten Industrien
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  Kenntnisse im Umgang mit Prozessleitsystemen
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  Abgeschlossene CPT- oder CPP-Lehre oder Bereitschaft, diese Ausbildung zu beginnen

KI-Beschreibung

In dieser Rolle als Automation Lead Engineer bist du für die Planung und Umsetzung von Automatisierungsprojekten verantwortlich. Du arbeitest eng mit interdisziplinären Teams zusammen, übernimmst die technische Verantwortung in allen Projektphasen und stellst sicher, dass alle GMP- und Sicherheitsvorschriften eingehalten werden.

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  Abgeschlossenes Studium als Ingenieur*in in Elektro-, Automations- oder Systemtechnik
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  Mehrjährige Erfahrung im Betrieb, in der Instandhaltung oder im Anlagenbau in einem GMP-regulierten Umfeld
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  Sehr gute Deutschkenntnisse in Wort und Schrift, gute Englischkenntnisse

Deine Vorteile

KI-Beschreibung

In this strategic leadership role, you will drive safety, sustainability, and site protection at the Visp site, influencing stakeholders and shaping a resilient organization that prioritizes people, assets, and the environment.

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  10+ years of experience in biopharma or pharmaceutical industry
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  Proven experience in project management
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  Deep understanding of cGMP and safety processes

KI-Beschreibung

In this strategic leadership role, you will drive safety, sustainability, and site protection at the Visp site, influencing stakeholders and shaping a resilient organization that prioritizes people, assets, and the environment.

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  10+ years of experience in biopharma or pharmaceutical industry
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  Proven experience in project management
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  Deep understanding of cGMP and safety processes

KI-Beschreibung

In dieser Rolle übernimmst du die fachliche Leitung eines EMR-Subteams und bist verantwortlich für die Planung und Umsetzung von Automatisierungsprojekten. Dein Alltag umfasst die technische Verantwortung über alle Projektphasen sowie die Sicherstellung einer zuverlässigen Instandhaltung im GMP-regulierten Umfeld.

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  Abgeschlossenes Studium als Ingenieur*in (ETH, FH, HF) in Elektro-, Automations- oder Systemtechnik
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  Mehrjährige Erfahrung im Betrieb, in der Instandhaltung oder im Anlagenbau in einem GMP-regulierten Umfeld
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  Sehr gute Deutschkenntnisse in Wort und Schrift, gute Englischkenntnisse

Deine Vorteile

KI-Beschreibung

You will manage IT infrastructure services while collaborating with teams to implement solutions. Your role involves driving automation, ensuring security, and maintaining documentation for efficient operations.

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  5 plus years of experience
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  Technical lead for infrastructure services
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  Fluent in German and English

KI-Beschreibung

In this role, you will craft and implement category strategies for Maintenance, Repair, and Operations while collaborating with stakeholders. The focus will be on driving supplier performance, optimizing inventory, and ensuring compliance with procurement standards.

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  10+ years of experience in international procurement and matrix environments
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  Experience implementing Capex/
  Opex MRO strategies in global organizations
• •
  Master’s degree in Business Administration, Legal, Applied Economics, Engineering, or Procurement

Deine Vorteile

KI-Beschreibung

In this role, you will lead technology transfers and process implementations while collaborating with cross-functional teams. Your day-to-day responsibilities will involve resolving manufacturing issues, interacting with customers, and driving continuous improvement in process performance.

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  More than 5 years of experience in biopharma manufacturing or process development
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  GMP and deep understanding of bioprocess technology
• •
  Master's degree, PhD, or equivalent experience

Deine Vorteile

KI-Beschreibung

You play a key role in developing user requirements and ensuring system compliance through validation activities. Your expertise supports audits, troubleshooting, and continuous improvement efforts.

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  Minimum 10 years experience in CSV
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  Strong understanding of GAMP 5 principles
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  Proficiency in German is required

Deine Vorteile

KI-Beschreibung

As a Material Requirements Planner, you will play a crucial role in ensuring materials are available to support production. Your daily responsibilities will involve collaborating with various teams, managing material plans, and optimizing inventory to meet supply needs.

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  Minimum of 5 years experience as a Material Requirement Planner
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  Degree or equivalent experience in SCM, Procurement, or relevant field
• •
  Required CPIM certification

Deine Vorteile

KI-Beschreibung

As an OT Security Architecture Lead, you will design and implement robust cybersecurity frameworks, ensuring systems meet security best practices while addressing gaps and enhancing cloud security. This role involves evaluating architectures and determining necessary protections for information systems.

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  Bachelor or Master in Computer Science, Cyber Security, or similar experience
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  Knowhow in IT network, Cloud solutions, and application security
• •
  6-10 years of relevant experience

Deine Vorteile

KI-Beschreibung

You manage supply chain systems by overseeing project execution, ensuring effective communication with stakeholders, and driving continuous improvement in processes and data management while maintaining regulatory compliance.

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  8+ years of experience in commercial pharmaceutical/
  biotech
• •
  Completed multiple SAP S/
  4 HANA implementations
• •
  PMP or similar project management certification

Deine Vorteile

KI-Beschreibung

In this role, you will spearhead internal improvement projects aimed at strategic growth, collaborating closely with the Director of Operations to enhance project execution practices and ensure operational excellence across the Advanced Synthesis platform.

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  Master’s degree or equivalent experience in Engineering, Chemistry, Biologics, or related scientific field
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  At least 5-10 years pharma proven experience
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  Extensive experience in cGMP chemical and/
  or biotechnological pharma engineering and manufacturing

Deine Vorteile