Qa-Stellen in Visp

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

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

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

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

Lonza

Are you a quality-focused professional looking to safeguard the integrity of high-impact life sciences manufacturing? Join our team in Visp as a Quality Batch Record Reviewer, where your attention to detail ensures every medicine meets the highest compliance and safety standards before release. This

Lonza

Are you a quality-focused professional looking to safeguard the integrity of high-impact life sciences manufacturing? Join our team in Visp as a Quality Batch Record Reviewer, where your attention to detail ensures every medicine meets the highest compliance and safety standards before release. This

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

MANPOWER AG – Your career, our focus! Become part of our network and take advantage of countless opportunities! ManpowerGroup is the world's leading company for workforce solutions. With our three brands – Manpower, Experis, and Talent Solutions – we support companies from various industries with th

Proclinical

pJoin a transformative GMP expansion project and make a lasting impact through validation, compliance, and quality excellence. /ppProclinical is seeking a QA Validation Specialist to support a major expansion project in Switzerland. This role focuses on ensuring that GMP equipment, facilities, and s

Lonza

pbLocation: /b the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ppWe are looking for a (Senior) QA Specialist Qualification (f/m/d), who will support our team QA Plant Qualification. /pppbbWhat you wil

Swisslinx

Job Description As a QA Logistic Specialist, you will ensure that incoming materials are verified and qualified in accordance with applicable GMP requirements, corporate standards and established service agreements. Based onsite in Visp five days per week, you will oversee the quality and compliance