Notes sur les cookies

Nous utilisons des cookies sur ce site web. Certains d'entre eux sont nécessaires au fonctionnement du site, comme les cookies techniques et fonctionnels. D'autres types de cookies, que vous pouvez refuser d'utiliser, sont les cookies de profilage de tiers. En cliquant sur "Accepter tous", vous consentez à l'utilisation de tous les cookies du site. En cliquant sur le bouton "Configurer", vous pouvez sélectionner vos préférences.

Accepter tous
Configurer
Seulement les nécessaires
header backgorund

Trouvez votre emploi avec Axepta SA

QA Supervisor

Axepta SA
Suisse, Vaud, Vaud - Axepta SA
Pharmaceutique
Autre

Our client, a growing and global medical device company located in Fribourg canton is looking for a QA supervisor to join their team for a new challenge. This person will help to create a new manufacturing line and built the team.   YOUR MISSIONS:   ·        Lead the quality strategies in the context of a new manufacturing area ·        Lead the Quality Assurance project team and help to uild up the new QA team for this area ( 2 people for 2025) ·        Provide conformity and application of the QMS for the project. ·        Ensure audits and regulatory inspections in the context of the project. ·        Collaborate actively with the business partners. ·        Provide leadership to build up the quality aspect of the project.   YOUR EXPERIENCE :   ·        Bachelor or Master in Biology, Pharmaceutical, medical device or related domain ·        At least 5 years of experience in Quality Assurance, including ideally 3 years in a management role. ·        Strong understanding of ISO Norm 13485, the European Directive 98/79/CE and FDA ·        Strong experience in QA strategies in projects ·        Strong leadership, people management and coaching skills. ·        Experience with project management, Lean or Six Sigma projects preferred. ·        French or German as a native language, with good knowledge of the other language. ·        English on a professional level.

...
Nouveau!
23/02/2024

QA Coordinator

Axepta SA
Suisse, Fribourg, Fribourg - Axepta SA
Pharmaceutique
Autre

Our client, a growing and global medical device company located in Fribourg canton is looking for a QA supervisor to join their team for a new challenge. This person will help to create a new manufacturing line and built the team. YOUR MISSIONS:   ·        Lead the quality strategies in the context of a new manufacturing area ·        Lead the Quality Assurance project team and help to uild up the new QA team for this area ( 2 people for 2025) ·        Provide conformity and application of the QMS for the project. ·        Ensure audits and regulatory inspections in the context of the project. ·        Collaborate actively with the business partners. ·        Provide leadership to build up the quality aspect of the project.   YOUR EXPERIENCE :   ·        Bachelor or Master in Biology, Pharmaceutical, medical device or related domain ·        At least 5 years of experience in Quality Assurance, including ideally 3 years in a management role. ·        Strong understanding of ISO Norm 13485, the European Directive 98/79/CE and FDA ·        Strong experience in QA strategies in projects ·        Strong leadership, people management and coaching skills. ·        Experience with project management, Lean or Six Sigma projects preferred. ·        French or German as a native language, with good knowledge of the other language. ·        English on a professional level.

...
Nouveau!
23/02/2024

QA Coordinator

Axepta SA
Suisse, Neuchâtel, Neuchatel - Axepta SA
Pharmaceutique
Autre

Our client, a growing and global medical device company located in Neuchatel canton is looking for a QA supervisor to join their team for a new challenge. This person will help to create a new manufacturing line and built the team. YOUR MISSIONS:   ·        Lead the quality strategies in the context of a new manufacturing area ·        Lead the Quality Assurance project team and help to uild up the new QA team for this area ( 2 people for 2025) ·        Provide conformity and application of the QMS for the project. ·        Ensure audits and regulatory inspections in the context of the project. ·        Collaborate actively with the business partners. ·        Provide leadership to build up the quality aspect of the project.   YOUR EXPERIENCE :   ·        Bachelor or Master in Biology, Pharmaceutical, medical device or related domain ·        At least 5 years of experience in Quality Assurance, including ideally 3 years in a management role. ·        Strong understanding of ISO Norm 13485, the European Directive 98/79/CE and FDA ·        Strong experience in QA strategies in projects ·        Strong leadership, people management and coaching skills. ·        Experience with project management, Lean or Six Sigma projects preferred. ·        French or German as a native language, with good knowledge of the other language. ·        English on a professional level.

...
Nouveau!
23/02/2024
9
8
7
6
5
4
3
2
1
TOTAL 86

Offres d'emploi totales:

énumérer tout
énumérer tout
énumérer tout
énumérer tout