QA Manager — Lonza
- Lieu
- Visp
- Contrat
- full-time
- Publié
- il y a 4 jours
Vue d’ensemble du poste
The actual location of this job is in Stein, Switzerland.
Relocation assistance is available for eligible candidates and their families, if needed.
In order to support our business growth in Stein (Switzerland), we are looking for a Quality Assurance Manager with expertise in Drug Product systems qualification, QC analytical equipment qualification and CSV & Automation.
- The actual location of this job is in Stein, Switzerland.
- Relocation assistance is available for eligible candidates and their families, if needed.
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities What you’ll get: An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance What you will do:
Responsabilités principales
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities What you’ll get: An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance What you will do:
- Responsible for Equipment, QC, Computerized System Validation (CSV) and Automation deliverables for new aseptic facilities, equipment and utilities related to the GMP manufacturing of drug products
Processus de candidature
- now.
- Lonza is a global leader in pharma and biotech manufacturing.
- The company operates major production facilities in Visp (Valais), Basel, and Stein (Aargau), Switzerland.
Entreprise et contexte
- Representing Quality in the CAPEX project organization in regards to Equipment, QC, Computerized System Validation (CSV) and Automation and Automation
- Reviewing and releasing quality related to Equipment, QC, Computerized System Validation (CSV) and Automation project deliverables
- Ensuring Equipment, QC, Computerized System Validation (CSV) and Automation deliverables meet Global procedures, regulatory requirements and policies
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders What we are looking for:
- Bachelor or Master degree in computer science, engineering, life science or related field
- Significant experience in the GMP regulated pharmaceutical industry project; preferable in a role within a Quality Unit
- Knowledgeable in commissioning and qualification of aseptic manufacturing systems and QC analytical systems, Annex 1 requirements
- Knowledgeable in CSV, Data Integrity, Automation systems and related Guidelines (21 CFR Part 11, EU GMP Annex 11, GAMP5 and the underlying principles of each)
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.) Sound knowledge of MES and DCS is required
- Fluency in English, German would be an advantage
Détails supplémentaires
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders What we are looking for:
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.) Sound knowledge of MES and DCS is required
Notes et contenu original
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities
- What you’ll get:
- An agile career and a dynamic work culture
- An inclusive and ethical workplace
- What you will do:
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders
- What we are looking for:
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.)
- Sound knowledge of MES and DCS is required
Questions sur cette offre
Quel salaire propose Lonza pour ce poste ?
Lonza indique CHF 85 500 - 129 500 bruts par an pour ce poste à Visp. Il s'agit du salaire publié dans l'annonce d'origine (ou, si l'employeur ne précise pas de montant, d'une estimation réaliste pour le rôle et le secteur) — le calculateur de ce site le convertit en net réel une fois l'impôt frontalier et les cotisations sociales appliqués.
Est-ce un poste à temps plein, et quel type de contrat propose Lonza ?
Cette offre est un poste en temps plein. Le type de contrat affiché ici provient directement de l'annonce originale de l'employeur ; confirmez toujours les horaires exacts, le préavis et la durée d'essai avec Lonza pendant le processus de candidature, ces détails pouvant varier même au sein de la même catégorie de contrat.
Ai-je besoin d'un permis de frontalier pour un poste dans le canton de Valais ?
Les résidents UE/AELE domiciliés dans la zone frontalière du pays voisin du canton de Valais peuvent demander un permis G ; l'employeur suisse le dépose auprès de l'office cantonal des migrations après signature du contrat. Les règles de zone frontalière et les délais varient selon le pays voisin et le canton — confirmez les détails auprès de l'office des migrations du canton de Valais ou avec les RH pendant la candidature.
Comment postuler à ce poste chez Lonza ?
Utilisez le bouton « Postuler maintenant » sur cette page — il renvoie directement à l'annonce originale de Lonza sur lonza.wd3.myworkdayjobs.com, votre candidature arrive donc directement dans le système de suivi des candidatures de l'employeur. Frontaliere Ticino ne collecte ni ne transmet lui-même les candidatures.
