Aktuelle Jobs im Zusammenhang mit Quality Assurance and IT Specialist - Neuenburg, Neuenburg - gloor&lang AG
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vor 24 Stunden
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Quality Project Manager
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Neuenburg, Neuenburg, Schweiz Axepta SA VollzeitNotre client, une entreprise pharmaceutique avec de beaux projets, recherche actuellement un Senior Quality Project Manager pour travailler sur des projets stratégiques de la compagnie situé sur le canton de Neuchâtel.VOS MISSIONS :- Être représentant pour les activités Qualité dans les projets clés du site, en coordonnant entre les équipes QA,...
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Quality Project Manager
vor 4 Wochen
Neuenburg, Neuenburg, Schweiz Axepta SA VollzeitPrésentation du posteNous recherchons un Sénior Quality Project Manager pour travailler sur des projets stratégiques dans le canton de Neuchâtel.MissionsRépéter les activités Qualité dans les projets clés, en coordonnant entre les équipes QA, Conformité, Qualité Fournisseur et Affaires Réglementaires.Être le point de contact avec les clients...
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Pharmaceutical Engineering Specialist
Vor 2 Tagen
Neuenburg, Neuenburg, Schweiz Randstad VollzeitAbout the Job DescriptionWe are seeking a skilled Pharmaceutical Engineering Specialist to join our team at Randstad.The ideal candidate will have a strong background in mechanical or chemical engineering and experience working with aseptic filling equipment, lyophilizers, isolator technologies, CIP/SIP systems, and sterile filtration processes.You will work...
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Quality Project Manager
vor 4 Wochen
Neuenburg, Neuenburg, Schweiz Axepta SA VollzeitNotre client, une entreprise pharmaceutique avec de beaux projets, recherche actuellement un Senior Quality Project Manager pour travailler sur des projets stratégiques de la compagnie situé sur le canton de Neuchâtel.VOS MISSIONS :- Être représentant pour les activités Qualité dans les projets clés du site, en coordonnant entre les équipes QA,...
Quality Assurance and IT Specialist
vor 2 Wochen
As a QA IT MES Specialist at gloor&lang AG, you will be responsible for ensuring excellence and compliance during the implementation of an electronic batch record system.
- Represent quality in site and global project teams, providing oversight and expertise on CSV and validation activities.
- Ensure all quality aspects of the project comply with Global Policies, SOPs, and GMP regulations.
What You'll Bring
- Proven experience in Computerized System Validation (CSV) and a strong understanding of cGxPs and industry standards.
- Fluency in English and French is essential.
