Qa-Stellen in Visp

Real

QA Validation & Qualification 1523 For our client, a leading global biotechnology and biopharmaceutical manufacturing company, we are looking for an experienced QA Validation & Qualification/ Cleaning SME: In this role, you will ensure GMP-compliant validation activities across manufacturing

Gi Group

The QA Validation Manager is responsible for ensuring all critical GMP processes are validated and maintained in compliance with product requirements, process parameters, and global regulatory guidelines. The role works closely with MSAT, Manufacturing, and clients to provide scientifically sound, d

Lonza

Location: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As a Senior Quality Assurance (QA) Specialist (f/m/d) for Analytics, you will ensure the Quality oversight on GMP-relevant activities carried o

Panda International

QA Validation Manager – Visp, Switzerland 🇨🇭 Location: Visp, Switzerland – Onsite Contract: Until the end of 2026 Extension: Option to renew The Role We are looking for an experienced QA Validation Manager to join a pharmaceutical/biotechnology environment in Visp. The successful candidate will pr

Proclinical Staffing

Join our client and play a key role in maintaining top-tier quality standards! If you have a keen eye for detail and a passion for compliance, this could be your perfect opportunity. Proclinical is seeking a QA Validation Manager to oversee and ensure compliance of critical GMP processes with produc

Lonza

Switzerland, Visp Location: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As a member of the QA Operations Team, the Senior QA Specialist (f/m/d) supports project preparation, execution and close out of campaigns. He/she will be the poin

Lonza

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The QA Manager (f/m/d) within QA Analytics is ensuring that all processes within the QC functional areas comply with GxP, data integrity and re

Lonza

Location: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As a member of the QA Operations Team, the Senior QA Specialist (f/m/d) supports project preparation, execution and close out of campaigns. He/she will be the point of contact for b

Lonza

QA Specialist (Projects) Join our dynamic Quality Assurance team in Visp to lead quality, compliance, and regulatory standards across groundbreaking biopharmaceutical customer and facility projects. In this role, you will play a critical part in delivering life-changing medicines to patients worldwi

Hays

QA Validation Manager The QA Validation Manager is responsible for ensuring all critical GMP processes are validated and maintained in compliance with product requirements, process parameters, and global regulatory guidelines. The role works closely with MSAT, Manufacturing, and clients to provide s

Lonza

Switzerland, Visp Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. We are looking for an experienced QA Manager, Lab Qualification (f/m/d) to join our QA Lab Qualification team in Visp. This r

Lonza

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. We are looking for an experienced QA Manager, Lab Qualification (f/m/d) to join our QA Lab Qualification team in Visp. This role combines hands

Lonza

Switzerland, Visp Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchan

Lonza

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our peo

CONSULTYS

Consultys Switzerland is looking for a QA professional to support our client, a biopharmaceutical manufacturing site in Visp, Switzerland. The role focuses on verification and release of incoming raw material batches, as well as the management of associated deviations and quality records. Key respon

CONSULTYS

Consultys Switzerland is looking for a QA professional to support our client, a biopharmaceutical manufacturing site in Visp, Switzerland. The role focuses on verification and release of incoming raw material batches, as well as the management of associated deviations and quality records. Key respon

Lonza AG

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. F or our site in the heart of the Swiss Alps, we are looking for a SeniorQA Specialist (m/f/d) MaterialManagement to join our team. In this rol

Lonza

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. For our site in the heart of the Swiss Alps, we are looking for a Senior QA Specialist (m/f/d) Material Management to join our team. In this ro

Aristo Group

Job Start Date - 10/08/2026 Job End Date - 31/12/2026 Description: Making sure the batch was made properly, according to procedure and regulatory requirements. Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process t

Purpose of the Role Responsible for reviewing executed paper-based batch records to ensure manufacturing activities were performed according to GMP procedures, internal SOPs, and regulatory requirements. The role requires strong attention to detail, independence, and a solid understanding of pharmac