QA Specialist

Pour notre client basé à Corsier-sur-Vevey, au seinde l'équipe QA Operations, nous sommes à la recherche de plusieursQA Operations Specialist pour une durée de 12 à jusqu'à 24 mois. QA pour les déviations etdonner les requis pour les les enquêtes/investigationassociées. ...

Nous recherchons pour l'un de nos prestigieux clients un .Poste basé dans le Nord Vaudois sur site de production / biotech.Revue par exceptions de dossiers de lots électroniques.Suivis de déviations en production.Vous justifiez d'au moins 2 ou 3 ans d'expérience en revue ...

For our client Merck in Aubonne, we are looking for aQA Specialist for QC (m/f/d) for a period of 12 months from1st September 2024. QA Oversight onQC analytical data:. To perform the QAreview on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA asQA. ...

Start date: September 2024Duration: 6-12 monthsLocation: Aubonne, Switzerland Actively participate to the daily activities of the QA Drug Substance teamPerform routine batch record review on time in order to support production needs in a fast-paced quality environmentYou will get insight in quality ...

We are currently searching for a QA Specialist - Project Manager for one of our clients, a global bio-pharmaceutical company located in Switzerland. ...

Receiving, reviewing, and processing customers feedback while using Good Documentation Practices.Processing complaints through classification of complaints, contact and product follow ups, maintaining investigation records and all other supporting documentation, and complete/assign additional action...

QA Operations Specialist 80-100% (m/f/d). The role will manage QA operational activities to support departmental projects and objectives according to agreed timelines and standards and ensure compliance with GMP is maintained in Sterile Production Plant Stein. Then, after the project phase, will man...

Pour notre site de Mont-sur-Lausanne, nous recherchons un Spécialiste QA(h/f/d) pour maintenir notre Système de Gestion de la Qualité. Connaissance dans le domaine QA dans l'industrie pharmaceutique ou des dispositifs médicaux (min. ...

Contributeto CSV strategies, plans, and protocols in accordance withregulatory As a QA IT CSV Engineer, you will be responsible forensuring compliance for computerized systems and computerizedsystems validation, fulfill with regulatory requirements andoperate as intended. Bachelor's degree in Comput...

Our client is a company in the manufacture and distribution of medicines, and veterinary products, with a wide range of products for farm animals and for pets. Determine the marketing strategy for the veterinary products in your portfolio. Elaborate the marketing plan, develop product communication ...