17 specialist English-speaking jobs in Visp

We are looking for a Raw Material Compliance Specialist for a pharmaceutical laboratory based in the ... Start date : June 2026 Duration : 5 months RAW MATERIAL COMPLIANCE SPECIALIST - Temporary position Role ... The specialist will work on several systems including SAP, TrackWise and the document management system ... : The raw material support specialist provides essential site support as part of the QA supplier management

For our campus in the heart of the Swiss Alps, we are looking for a(Senior)QA Specialist,MaterialManagement

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.

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

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

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.

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.

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.

qualification Proven experience in pharmaceutical or chemical manufacturing environments Swiss safety specialist

The Batch Record Review Intern supports the Quality Assurance team by reviewing, verifying, and organizing electronic GMP manufacturing documentation. This role involves reviewing executed batch records, clarifying comments, and supporting deviation and investigation processes.

Leads and shapes a comprehensive contamination control strategy within a GMP-regulated bioconjugates environment, ensuring end-to-end compliance across manufacturing facilities. Drives cross-functional collaboration, manages risk assessments, change requests, deviations, investigations, and CAPAs. Authors and approves GMP documentation, including SOPs, deviations, change controls, and risk assessments. Partners with cross-functional teams to identify risks, drive deviation management, and strengthen contamination prevention control practices. Acts as a QA Microbial Contamination Control and cleaning SME in meetings, audits, and inspections. Reviews and approves routine cleaning-relevant documents and finalizes records like SOPs, MBRs, Material Specifications, Deviations, Change Requests, Effectiveness Checks, Testing Protocols & Reports. Identifies emerging QA relevant topics and communicates with stakeholders, working on their development into new or existing Quality and Compliance strategies and/or standards. Supports continuous improvement programs to establish effective Quality Contamination Control.

Design, build, and enhance SAP EWM solutions supporting warehouse and labeling operations. Act as an IT business partner, translating business needs into functional specifications. Configure and customize SAP EWM in line with global processes and governance. Provide third-level support for complex system incidents and problems.