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

You will drive strategic partnerships by overseeing vendor selection and performance while ensuring smooth operations through effective governance and collaborative RFP processes.

• •10 years experience in alliance management or equivalent
• •Expertise in contract negotiations and issue resolution
• •Knowledge of clinical operations and drug development

Deine Vorteile

KI-Beschreibung

In this high-impact field role, you will drive innovation for drug-device products by bridging the gap between R&D and global pharma partners to secure complex, high-value projects.

• •Experience in developing PFS and injection devices
• •Experience with drug–device combination products
• •Knowledge of injectable products, delivery systems, and medical device commercialization

Deine Vorteile

KI-Beschreibung

You will spearhead the strategic and financial growth of the Peripheral Intervention unit across Europe, leading a diverse team to drive commercial success and market expansion.

• •General management and P&L experience
• •Proven medical devices market experience
• •Significant Sales and Marketing experience

Deine Vorteile

KI-Beschreibung

In this role, you will drive the IV Fluids portfolio by combining financial analysis with strategic planning to optimize the global market presence and supply chain.

• •Minimum 5 years experience in IV Fluids
• •University degree in Science, International Business, or Business Administration
• •Understanding of Regulatory Affairs and Finance

KI-Beschreibung

In this role, you will spearhead marketing strategies across EMEA, driving product commercialization and leveraging analytics to inform decisions. Your leadership will shape the future of life science research while nurturing a talented team.

• •Proven experience in marketing leadership within life sciences, biotechnology, or related fields
• •Strong track record in product launches, commercialization, and market development
• •Deep understanding of Flow Cytometry, Single-Cell Multiomics, or advanced research technologies

Deine Vorteile

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

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 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

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

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

As a Production Intern, you will engage in continuous improvement initiatives, tackling challenges from waste reduction to optimizing tooling. Your day-to-day responsibilities will involve analyzing processes, implementing solutions, and measuring their impact on performance.

• •Hands-on experience and ability to implement solutions
• •Lean Manufacturing and 5S skills
• •Python, Power BI, Solidworks, Anylogic skills

KI-Beschreibung

As a Machinery Safety Specialist, you will ensure machine safety excellence by leading safety programs, conducting risk assessments, and collaborating with various teams. This role involves identifying hazards, supporting compliance, and fostering a strong safety culture within the packaging department.

• •Master’s degree in mechanical, electrical, automation engineering, safety engineering, or equivalent
• •3–5 years of experience in machinery safety, engineering, industrial safety, or EHS roles within an industrial environment
• •Expertise in ISO 12100, ISO 13849, EN 60204

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 engage with cutting-edge technology while operating automated machines in a dynamic pharmaceutical production environment. You will work closely with a diverse team, focusing on quality and safety as you explore the exciting world of production line operations.

• •Interest in mechanics, robotics, and teamwork
• •Passion for mechanics and new technologies
• •Mastery of French

Deine Vorteile

KI-Beschreibung

In this role, you will manage key enterprise accounts, focusing on driving performance and client satisfaction. Your day-to-day responsibilities will involve building relationships, negotiating renewals, and identifying growth opportunities while collaborating with various internal teams.

• •5+ years of experience in B2B Account Management
• •Proven track record in managing large or complex customer accounts
• •Fluency in English and German (written and spoken)