Carries out manufacturing tasks in the Drug Product area in compliance with cGMP guidelines, ensuring successful batch execution, assessing test results, addressing issues, troubleshooting manufacturing… Leggi tutto »Biotechnologist/GMP (m/f/d)
The Commissioning Qualification Validation engineer carries out a variety of tasks related to the validation of equipment and facilities. Duration: Until 01/03/2025. Possible extension Location:… Leggi tutto »CQV Specialist (m/f/d)
Do YOU want to support improving the logistic depatment of an pharmaceutical company? Then join the team of our client in Valais and help improving… Leggi tutto »Logistic Process Specialist (m/f/d)
Our client in Visp is seeking a Planner with experience with ‘Operational Readiness’ to support the Capital Projects. This position will be directly responsible for… Leggi tutto »Operational Planner (m/f/d)
Holds all quality related responsibilities for daily qualification activities on technical facilities, equipment and systems Supports the development, reviews and releases qualification documents. Approves applicable… Leggi tutto »Quality Engineering Specialist (m/f/d)
For our client in Valais, we are looking for a Biotechnologist who will support their growth in several business units. Start date: September 2024 End… Leggi tutto »Biotechnologist (m/f/d)
We are looking for a QC expert who will perform and release in-process controls (UV, GC, titrations, pH, HPLC, etc.) in compliance with cGMP guidelines… Leggi tutto »Quality Control Analyst (m/f/d)
For our client, we are looking for a Quality Engineering Specialist who will hold all quality related responsibilities for daily qualification activities on technical facilities,… Leggi tutto »Quality Engineer (m/f/d)
For our client, a leading company in the Chemical Manufacturing field, we are currently looking for a Project Manager (IT Manufacturing department) Your Responsibilities: Responsible… Leggi tutto »Project Manager (Manufacturing) (m/f/d)
You will be in a close collaboration with the Bioprocess Engineers and Quality Assurance regarding the products produced and their good documentation practice Start date:… Leggi tutto »Batch Record Reviewer (m/f/d)