10 independent jobs found for you.

Caring for the world, one person at a time ?… inspires and unite the people of Johnson & Johnson, we embrace research and science- bringing innovative ideas, products and services to advance the health and well-being of people.Janssen Pharmaceutical is part of Johnson & Johnson and responsible for bringing innovative medicines towards patients throughout the world.Specific Responsibilities:Independent coordination (receiving, input, storage, disposal,

Are you ready to bring your deep professional experience to a team that truly values stability and specialized expertise in rehabilitation?We are seeking experienced Rehabilitation Nurses to join a respected healthcare facility in Kanton Thurgau on a permanent contract. Your career deserves a place where your commitment to patient recovery and professional competence are central to the mission.Secure a long-term position where your experience is highly

Are you ready to bring your deep professional experience to a team that truly values stability and specialized expertise in rehabilitation?We are seeking experienced Rehabilitation Nurses to join a respected healthcare facility in Kanton Thurgau on a permanent contract. Your career deserves a place where your commitment to patient recovery and professional competence are central to the mission.Secure a long-term position where your experience is highly

On behalf of our Client, an international pharma company based in canton Lucerne, we are looking for a dedicated and organized Logistics Specialist who enjoys international logistics, dealing with compliance issues and collaborating with internal and external partners.General Information: Start date: ideally June 2026Duration: 2 yearsExtension: possible, to be discussedContract: temporary contract via RandstadLocation: Schachen (LU)Workload: 100%Home

Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive

Project Lead (Technical / Engineering) – GMP EnvironmentVisp, Switzerland (On-site)Full-timeStart Date: No later than May 4, 2026About the RoleWe are looking for an experienced Project Lead to manage and deliver technical investment projects within a production environment. This role combines technical project management, engineering expertise, and cross-functional leadership to drive impactful improvements in production processes and business

Position Snapshot Location: Vers-chez-les-Blanc, SwitzerlandEntity: Clinical Research Unit, Nestlé ResearchWork rate: 100%Contract type: TemporaryDuration: 12 monthsSummaryThe Senior Clinical Trial Assistant (Sr. CTA) provides high-quality operational and administrative support to clinical trial teams throughout all phases of a pharmaceutical study. Operating within a fast-paced, regulated environment, the Sr. CTA ensures clinical documentation is

A leading telecommunication  company in Bern is looking for a DevOps Engineer CyberArk, PKI.Key requirements  DevOps Engineers I can independently implement simple backlog items or backlog items with a focus on their area of ??expertise with little guidance.-Creating and refining backlog items together with the product owner, estimating backlog items as a team and planning for the next iteration.- Ensure built-in quality and built-in security of their

Love complex problems? We’re looking for a OneStream Architect who does more than just configure. We need a seasoned pro with 5+ years of experience and a deep command of C#/VB.NET and Financial Consolidation to lead high-stakes implementations. If you’re a hands-on developer who thrives on building elegant solutions to intricate financial workflows, we want you on the team.General Information:Start date: 01.06.26latest Start Date: 01.09.26Planned

For one of our clients, an international pharmaceutical company, we are seeking a Computer System Validation Engineer.General Information:Start date: 01.05.2026End Date: 31.10.2026Workplace: Schachen, LuzernHome office: No, 100% onsiteWorkload: 100%Working hours: StandardAbout the work:Our client’s Metrology and Validation department in Analytical R&D (AR&D), located in Schachen, is currently looking for a scientist or engineer with a background in