The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing Operations and
Overview Are you passionate about quality, precision, and working in a GMP-regulated environment? We are currently seeking a detail-oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment. The
Job Title: IT Systems Engineer / IT Support Job Type: Full-time Location: Lucerne, Switzerland (Hybrid) We have partnered with a highly dedicated IT services provider based in Switzerland to find their next IT Support Specialist (Windows
Product Owner - An International SaaS - Lucerne, Switzerland (Key skills: Product Owner, SaaS Product Management, Contract Lifecycle Management, User Stories, Backlog Management, Scrum, Kanban, Cloud/Web Solutions, Stakeholder Management, Roadmap Planning, Compliance & Security, Product Release,
Manufacturing Engineering Team Lead | Medical Devices | Switzerland | Competitive Salary I am partnering with an innovative medical device manufacturer to appoint a Team Leader within their Manufacturing Engineering function. The company operates in an
GeoSolutions is looking for a Head of Engineering to help us coordinate, structure and grow our engineering organization while remaining deeply involved in technical decisions and delivery. This is a senior, hands-on leadership role. The ideal candidate
Manager Supply Chain Business Intelligence (Supply Planning) (m/f/d) Purpose & Overall Relevance for the Organization Are you enthusiastic about the prospect of driving excellence in reporting & analytics capabilities to increase transparency and visibility across the
About Our Client For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking a Batch Record Review Specialist (m/f/d). In this role, you will support clinical biologics
The Commissioning & Qualification Engineer role in the Metrology & Validation department, oversees and supports the qualification of analytical instrumentation and Computer Systems projects within the GMP environment. Responsibility of this function is to maintain the
Operator for Biotech Support Operations For one of our clients, an international pharmaceutical company, we are seeking an Operator for Biotech Support Operations . General Information: Start date: ASAP (high urgency) End Date: 1 year Home
Operator for Biotech Support Operations For one of our clients, an international pharmaceutical company, we are seeking an Operator for Biotech Support Operations . General Information: Start date: ASAP (high urgency) End Date: 1 year Home
At TELUS Digital , we are expanding our mission to include the physical world. We believe that for AI to be truly transformative, it must move beyond the screen and into the real world. As a
International pharma company 18 months contract with extensionoption About Our Client Our client is a well-established organization within the pharma industry, renowned for delivering innovative solutions and maintaining a strong commitment to quality and compliance. Operating