43 qa-Stellen in Visp heute aktualisiert
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Gi GroupThe 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
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
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
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
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
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
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
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
HaysQA 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
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
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
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
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
CONSULTYSConsultys 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
CONSULTYSConsultys 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
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
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
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
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
CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when
The Life Science Career Network CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes. Manag
QA Batch Record Reviewer (German-speaking) Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a QA Documentation Specialist for a contract position till end of 2026 (with option
The Life Science Career Network CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes. QA Va
The Life Science Career Network CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes. QA Va
This role requires the candidate to work remotely on a part-time basis from France. Client Overview Our client is a global artificial intelligence technology company specializing in the development of advanced large language models (LLMs), speech recognition technologies, multilingual AI systems, an
QA Batch Record Reviewer (German-speaking) Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a QA Documentation Specialist for a contract position till end of 2026 (with option
SGIQA Validation Specialist (Fixed-Term Contract) We are seeking an experienced QA Validation Specialist to support a major biologics manufacturing expansion project in canton Valais. You will play a key role in ensuring GMP equipment, facilities, and systems remain qualified, validated, and inspection
Recrutis is supporting a leading biopharmaceutical manufacturing site in Valais, Switzerland, in the search for a QA Validation Specialist, based on site in the Valais region. Why this role QA ownership of qualification and validation activities on a large-scale mammalian cell culture and biologics
CHF 38'000 – CHF 61'000/Jahr
Schatzungsvertrauen: Niedrig
Schatzung basierend auf Marktdaten für Visp. Tatsachliche Gehalter konnen je nach Erfahrung, Unternehmen und Gebiet variieren.
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