49 specialist English-speaking jobs in Canton of Valais

Manufacturing Specialist will perform upstream or downstream manufacturing activities following cGMP guidelines. Troubleshoot equipment, evaluate test results, and recommend solutions. Prepare and maintain documentation such as batch records and SOPs. Contribute to capital investment projects and equipment commissioning. Train manufacturing staff on equipment and standard operations.

About the Role We are looking for an IT Application Specialist with a strong foundation in system administration

The role: The Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements for manufacturing

duration: 6 months + likely extension Position Overview We are looking for a Raw Materials Support Specialist

We are looking for a Senior QA Specialist (m/f/d) to join multifunctional QA Operations team in the Bioconjugates

IT Administrator and Support Specialist provides maintenance and support for end users, equipment, software, servers, and networks. Processes requests and incidents, deploys and updates equipment and software, and ensures system security and availability.

Manufacturing Specialist will execute production steps, interpret deviations, and support training within a cGMP environment. Requires a chemical/biopharmaceutical education, experience in pharmaceutical production, and fluency in English. German language skills are advantageous.

To complete our teams, we are looking for a:Modern Workplace Specialist at 100%YOUR FUTURE MISSION- Manage

The QA Specialist (QA On The Floor) is responsible to the Associate Director, Head of QA Operations BioAtrium ... The QA Specialist will within the QA Operations team as QA On The Floor, but will support other QA Ops

Senior QA Specialist will provide quality assurance oversight for site and facilities, focusing on shared utility systems and logistics areas. Responsibilities include providing QA support, leading deviation review boards, and reviewing change requests and CAPAs.

Proclinical is seeking a QA Raw Material Compliance Specialist to join a dynamic team in Switzerland.

Manufacturing Specialist for Upstream or Downstream processing at Lonza's Visp site. Executes manufacturing activities according to cGMP guidelines, supports risk assessments, and assists with document preparation. Requires a chemical/biopharmaceutical education, knowledge of biotechnological processes, and fluency in English.

material compliance in a dynamic GMP environment.Proclinical is seeking a QA Raw Material Compliance Specialist

Proclinical is seeking a QA Raw Material Compliance Specialist to join a dynamic team in Switzerland.

Join us as a Manufacturing Specialist – Opportunities for All Experience Levels!

In the role of the Manufacturing Line Specialist - Anlagemeister (AM) you ensure through intensive technical

Senior MSAT Specialist will lead impurity risk assessments and develop control strategies for Small Molecules, ensuring compliance with ICH Q3D, Q3C, and Q9. This role requires strong analytical and communication skills, experience in GMP environments, and the ability to collaborate effectively across functions.

Reviews, assesses, and coordinates Vendor Change Notifications (VCNs) from suppliers. Ensures impact assessments are completed and VCNs are managed according to GMP requirements and regulatory expectations. Collaborates with internal stakeholders to support compliant supplier management.

Reviews, assesses, and coordinates Vendor Change Notifications (VCNs) ensuring compliance with GMP requirements and internal procedures. Manages VCNs, tracks documentation changes, and collaborates with stakeholders. Requires a Bachelor's or Master's degree in a scientific discipline and 5+ years of experience in QA, Supplier Management, or Change Control.

QA Raw Material Compliance Specialist needed to support the management of Vendor Change Notifications (VCNs). Responsibilities include reviewing, assessing, and coordinating the evaluation of VCNs, ensuring compliance with internal procedures and regulatory expectations. Requires a Bachelor's or Master's degree in a relevant field, 5+ years of experience, and strong understanding of GMP regulations and change control processes.