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Laborant

Manpower SA — Meyrin
26.03. | Temporary | 100%

Introduction :

Nous recherchons pour le compte de notre client un(e) laborant(e) à 100% pour une mission temporaire.

Référence filiales : 110-GEW CHIMIE & LIFE SCIENCES
Nom du conseiller : Bouillon Anne
Nom de la filiale : 3
Adresse :
4, rue Winkelried
Genève
1201

Description de l'entreprise :
Manpower, leader des solutions efficaces et innovantes pour l'emploi, met en relation les meilleurs talents du marché avec les entreprises recherchant des compétences précises. Chaque année, 5'000 clients dans tous les secteurs d'activité et 20'000 candidats nous font confiance. Avec plus de 400 collaborateurs internes et 60 filiales, Manpower Suisse est ancré dans toutes les régions linguistiques.
Secteur d'activité : Chimie & Life Sciences

Laborant

Description:

Nous recherchons pour le compte de notre client un(e) laborant(e) à 100% pour une mission temporaire.
Date d'entrée : 03-04-2020
Type de société : Entreprise privée
Reference : 101352-705-1
Date de publication : 2020-03-26 15:03:20
Profil recherché :
- Planifier les différentes étapes d'une expérience,- Préparer le matériel, les appareils, les échantillons à tester, en respectant les protocoles d'expérience,- Effectuer des prélèvements,- Extraire une substance en utilisant une opération appropriée (distillation, centrifugation, filtration, etc.),- Surveiller le déroulement des expériences en assurant les meilleures conditions de sécurité, - Utiliser les moyens informatiques pour enregistrer les données, rédiger les rapports d'expériences.

Pays : Suisse
Lieu de travail : MEYRIN 2
Code postal : 1217
Catégorie : Chimie
Niveau d'études : Expérience professionnelle : Début du contrat : 03.04.2020Durée du contrat : Non précisé
Conclusion :
Si vous correspondez au profil, merci de nous faire parvenir votre dossier à jour.

26.03.2020
Employee, 100%

Contact

Manpower SA


Manpower

Rue Winkelried 4Genève

Industry

Human resources / Personnel services

Year of foundation

1960

Labels (1)

Training Company
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Bioanalytical (Associate) Project Manager (based in Geneva) Key responsibilities Support clinical trial logistics and planning of human sample analysis in the laboratory, as related to bioanalytical activities. Ensure that smooth process of sample analysis is undertaken. Ensure back-up for other coordination members Liaise with different stakeholders (such as Bioanalytical project managers, Lab operators, clinical team, finance,) to maintain project schedules and follow-up project timelines in line with business objectives. Ensure proper and regular Trial Master File filing of documentation and Quality control check Organize Bioanalytical Meetings involving relevant stakeholders, and ensure meeting minutes recording and monitoring of follow-up actions. Review of clinical documentation (Patient’s Informed Consent Form, eCase Report Form, Clinical Protocols, Laboratory Manuals). Perform annual budget forecast preparation, including costs, resources allocation and provide information to the Finance department or Clinical Program Leaders as needed. Project management with external partners for outsourced work, including CRO selection, contracting, documentation review and support for study monitoring and closing. Coordinate CRO oversight meetings, prepare agenda, involve appropriate stakeholders, ensure meeting minutes recording and monitor follow-up actions. Ensure performance of service providers to achieve on time delivery of project milestones, within the budget. Ensure invoices are processed according to internal procedures (or requests from finance department) Participate in the creation, update and/or review of the Quality System documentation to improve/ implement processes in compliance with GCP/ GCLP. Participate in Quality Assurance audits of the bioanalytical facility Participate to the CAPA Plan actions execution as required Cooperate with Quality Assurance in the frame of the inspection readiness preparation Skills and Competencies A Bachelor’s Degree in a scientific discipline is required. At least 3 years of experience of project management in cross-functional projects in either Pharma/Biotech or CRO are required. Project management certification is a plus. Good knowledge of clinical studies, GCLP/ GCP environment. Team player, ability to work with others, to face challenges and solution-oriented. Excellent organizational skills, ability to prioritize tasks and to cover multiple concurrent activities Ability to work under pressure. Excellent communication skills, able to communicate at different levels within the organization. Excellent command of written and verbal English. French an asset.Swedish Orphan Biovitrum AGPlan-les-Ouates
02.04

Manpower

Rue Winkelried 4Genève

Industry

Human resources / Personnel services

Year of foundation

1960

Labels (1)

Training Company
Training Company
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