500+ Jobs in Coppet & Umgebung

KI-Beschreibung

In dieser Rolle bist du für die Durchführung und Überwachung spezialisierter chemischer Analysen verantwortlich. Dein Alltag umfasst die Wartung und Kalibrierung von Instrumenten sowie die technische Validierung der Ergebnisse.

• •Diplôme de Technicien(ne) en Analyses Biomédicales ES ou équivalent
• •Première expérience réussie en Chimie Clinique/Spéciale

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du für Wartungen und Kalibrierungen von automatisierten Analysegeräten verantwortlich. Du führst Qualitätskontrollen durch und dekantierst Proben, während du in einem flexiblen Schichtsystem arbeitest und eng im Team zusammenarbeitest.

• •Diplôme de Technicien(ne) en Analyses Biomédicales ES ou équivalent
• •Expérience en Chimie Clinique

Deine Vorteile

KI-Beschreibung

In dieser Rolle führst du Bakteriologieanalysen durch und achtest dabei auf die Einhaltung der Compliance-Kriterien. Du nutzt eine Verwaltungssoftware und kommunizierst effektiv auf Deutsch, während du sowohl selbstständig als auch im Team arbeitest.

• •Diplôme de Technicien(ne) en analyses Biomédicales ES
• •Expérience minimum de 2 ans en microbiologie médicale

Deine Vorteile

KI-Beschreibung

Du arbeitest präzise: Du validierst medizinische Analysen und erklärst die Ergebnisse den Kunden. Außerdem bewertest du neue Verfahren und setzt sie um, während du zuverlässige und qualitativ hochwertige Dienstleistungen sicherstellst.

• •Formation FAMH complétée en médecine de laboratoire
• •Capacité à travailler en équipe
• •Personnalité communicative avec compétences sociales

Deine Vorteile

KI-Beschreibung

As a Fragrance Claim Scientist, you will play a key role in developing and validating fragrance claims. You will collaborate with various teams to ensure compliance and scientific credibility while translating sensory experiences into compelling product stories.

• •Scientific or technical background
• •Understanding of regulatory and testing processes
• •Ability to interpret and communicate technical data

Deine Vorteile

KI-Beschreibung

As the Alliance and Sourcing Lead, you will manage key relationships with strategic partners, oversee vendor selection and performance, and drive the RFP process, all while ensuring smooth operations and innovative solutions.

• •At least 10 years of work experience in alliance management, CRO, vendor management, or equivalent experience in clinical outsourcing and pricing analysis
• •Graduate degree in a scientific, medical, or relevant business discipline
• •Strong expertise in contract negotiations and issue resolution

KI-Beschreibung

In this internship, you will support the evaluation and testing of prefilled syringes and elastomeric stoppers for biologic drug products. Daily tasks will involve conducting laboratory studies, analyzing data, and collaborating with team members to ensure quality and compliance.

• •Bachelor’s or Master’s in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Biochemistry, or related field
• •Experience with analytical tools (HPLC, HAIC, MFI, balance, etc.)
• •Ability to follow SOPs and work with precision

KI-Beschreibung

As an EMEA Demand Planner, you will play a crucial role in aligning business strategy with operational excellence, driving demand planning initiatives, and enhancing forecast accuracy to improve customer service and inventory management.

• •At least 3 years of experience in a similar role
• •Strong proficiency in SAP, Excel, PowerPoint, and Word
• •University degree or equivalent experience in Demand Planning, Supply Chain Management, Business, or related field

KI-Beschreibung

As a CMC Statistics Intern, you will engage in coding, statistical analysis, and machine learning to support biosimilar development. This role involves collaborating with scientists, ensuring data integrity, and contributing to daily CMC activities.

• •Master's program or equivalent in statistics, biostatistics, or data science
• •Knowledge of commonly used statistical methods: Anova with fixed or random effects, linear regression, ancova, non-linear models, R programming, knowledge in machine learning and model selection
• •Knowledge of biotech/pharma and high-level drug development process or high interest in scientific area

KI-Beschreibung

As the Marketing Director for Urology and Critical Care in Europe, you will lead the development and execution of innovative marketing strategies that drive growth and profitability. This role involves inspiring change, fostering collaboration, and ensuring a customer-centric approach while navigating the complexities of the healthcare market.

• •Significant depth and breadth of marketing knowledge and experience
• •Dynamic experience in marketing leadership in life sciences, medical devices, or healthcare
• •Ability to lead marketing organizations in diverse environments

KI-Beschreibung

As a Data Analyst Intern, you will play a key role in supporting the Business Intelligence Manager by consolidating sales data, preparing insightful reports, and analyzing trends. This position involves optimizing data management and ensuring accurate reporting for various stakeholders.

• •Bachelor’s degree in business administration, economics, or equivalent
• •Proficiency in Excel, PowerPoint, Outlook, and ideally Power BI knowledge
• •Experience or interest in luxury and fragrances industry

Deine Vorteile

KI-Beschreibung

In this role, you will ensure compliance with regulations for Medicinal Products while managing quality tasks and supporting GMP activities. Your day-to-day responsibilities will involve overseeing quality processes, conducting audits, and contributing to continuous improvement efforts.

• •5 years’ experience in Quality function in pharmaceutical industry
• •Strong understanding of GMPs, GDP, ICH guidelines
• •Significant experience as lead auditor for pharmaceutical manufacturing

KI-Beschreibung

As a Regulatory Affairs Specialist Intern, you will engage in various tasks, including preparing essential documents for marketing applications, managing regulatory databases, and supporting vendor agreements. This role is pivotal in ensuring compliance and facilitating smooth product lifecycle management.

• •Relevant diploma or degree in health sciences
• •Fluent command of spoken and written English
• •Basic knowledge of international standards in drug development or registration

Deine Vorteile

KI-Beschreibung

In this role, you will lead global regulatory strategies for biosimilars, guiding submission processes and ensuring compliance. Your day-to-day responsibilities will involve collaborating with teams, managing regulatory interactions, and developing staff to meet ambitious goals.

• •At least 15 years in international regulatory
• •Experience in managing international or regional regulatory submissions
• •Experience in people management and driving high performing teams

KI-Beschreibung

As an Associate Director of Quality Management, you will lead a quality team focused on contract manufacturing, ensuring compliance and driving continuous improvement while collaborating with various departments to enhance supplier capabilities.

• •10 years of senior experience in regulated industries
• •10+ years of experience in electromechanical instrumentation manufacturing
• •Deep knowledge of ISO 13485, FDA QSR, ISO 14971, and international medical device regulations

KI-Beschreibung

In this role, you will manage financial closings and forecasting while collaborating with various departments. Your day-to-day responsibilities will involve overseeing project costs, supporting trading hubs, and guiding teams on financial matters.

KI-Beschreibung

In this role, you will engage in routine laboratory analyses and contribute to method development for monoclonal antibodies. Daily activities will include recording experiments, participating in team meetings, and supporting documentation efforts.

• •CFC in biology, biotechnology, or pharma domain
• •Basic knowledge of physico-chemical analytical methods and/or antibodies
• •Experience in Word, Excel, PowerPoint, Outlook

KI-Beschreibung

As a Communication Intern, you will assess and enhance communication strategies while creating engaging content tailored for diverse regions. Your work will help standardize messaging and improve internal communications across a global landscape.

• •2nd or 3rd year student in communications, marketing, media, or journalism
• •Strong written and spoken English
• •Proficiency with digital tools for video creation and visual design

KI-Beschreibung

In this role, you will lead the development of innovative strategies and AI-driven solutions to enhance patient-focused analytics. Your work will involve collaboration across teams, building capabilities, and representing the organization in industry engagements.

• •PhD or advanced degree in Epidemiology, Biostatistics, Data Science, Computer Science, Engineering, Life Sciences related fields
• •10+ years of experience in RWE generation, advanced analytics, AI, technology, digital transformation, or business solutions
• •Expertise in statistical programming (e.g., R, SAS, Python) and working with diverse PRWD sources

KI-Beschreibung

In this role, you will define and implement regulatory strategies for biosimilars, ensuring compliance while managing submissions and interactions with health authorities. Your daily responsibilities will include collaborating with cross-functional teams and staying updated on regulatory changes to support project development.

• •5-8 years Regulatory Affairs CMC experience in Biotech
• •Master’s Degree in Life Science or related discipline
• •Experience in managing international regulatory submissions

KI-Beschreibung

In this role, you will lead device development projects from concept to production, collaborating with cross-functional teams to ensure quality and compliance. Your daily responsibilities will include managing timelines, budgets, and risks while driving innovation and improvement initiatives.

• •10+ years of experience in device development with understanding of device safety and regulatory requirements
• •5+ years of experience in project management
• •Experience in FDA regulated medical devices and combination drug device products

KI-Beschreibung

You will use your expertise in ServiceNow to design solutions, support application development, and ensure effective integration with external tools while promoting best practices and documenting requirements.

• •4 years of experience with ServiceNow
• •ServiceNow Administrator certification is required
• •Experience implementing 2 major ServiceNow modules

KI-Beschreibung

In this role, you will lead global regulatory efforts for biosimilars, guiding submission strategies and ensuring compliance. Your day-to-day responsibilities will involve collaborating with teams, managing interactions with health authorities, and mentoring junior staff.

• •At least 6-8 years in international regulatory
• •Experience in managing international or regional regulatory submissions, normally a full global submission (new product application), preferably US BLA or EU MAA
• •Experience in preparation and coordination of regulatory strategy plan

KI-Beschreibung

In this role, you will be the go-to HR expert for complex issues in Switzerland, managing everything from employee relations to compliance. Your day-to-day responsibilities will involve collaborating with various teams to ensure smooth HR operations and drive continuous improvement.

• •7+ years of progressive HR experience
• •Solid understanding of Swiss employment law, payroll, social security, and employee relations frameworks
• •Bachelor’s degree in Human Resources, Business Administration, or related field; Swiss HR certifications

KI-Beschreibung

As an IT Field Support Champion, you will be the first point of contact for resolving technical issues, ensuring user satisfaction while keeping IT systems running smoothly. This role involves problem-solving, providing user support, and engaging in continuous learning alongside seasoned professionals.

• •Completion of IT training, IT studies, or strong passion for technology
• •Ability to explain tech simply in French, ideally also in English; German is a plus
• •Enjoyment of helping others and ability to stay calm under pressure

Deine Vorteile

KI-Beschreibung

As a Team Leader, you will develop and guide a team of operators to achieve safety, quality, and performance goals. This role involves ensuring compliance, driving continuous improvement, and managing resources effectively across shifts.

• •5 years of experience in manufacturing/production
• •3–5 years of leadership experience in manufacturing or packaging
• •Experience in FDA‑regulated environments

KI-Beschreibung

In this role, you will be the vital link between the Nyon plant and its suppliers, managing quality assurance activities, handling complaints, and ensuring compliance with regulatory standards. Your day-to-day responsibilities will include overseeing documentation, participating in audits, and supporting supplier qualifications.

• •Minimum of 5 years industry experience
• •Minimum of 2 years full-time supplier related activities
• •Working knowledge of regulatory agency requirements

KI-Beschreibung

As a Production Intern, you will play a key role in enhancing performance by implementing continuous improvement solutions and utilizing HAPS tools. Your daily tasks will involve analyzing processes, optimizing tooling, and reducing waste to support the site's operational goals.

• •Hands-on experience
• •Ability to implement concrete solutions
• •Strong communication skills

KI-Beschreibung

In this role, you will collaborate with the Facility Management team to enhance daily maintenance processes, focusing on safety and operational efficiency. Your responsibilities include training technicians, analyzing downtimes, and supporting standardization efforts.

• •Problem solving skills
• •Analytical skills and ability to prioritize
• •Good communication skills

KI-Beschreibung

As an Environmental Engineer Intern, you will play a key role in supporting environmental initiatives, from analyzing industrial water flows to training employees on waste management practices. Your work will directly contribute to reducing environmental impact and ensuring compliance with standards.

• •Expertise in environmental risk management
• •Knowledge in water treatment
• •Knowledge in chemistry