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We are currently seeking a Validation engineer for one of our clients in Canton of Neuchatel.
If you are looking to work in a dynamic and very friendly working environment then this is for you.
This is an open-ended temporary contract
Please note this vacancy requires fluency in French.
Your responsibilities:
Generation and execution of qualification/validation protocols including the generation, routing and approval of summary documentation.
Work with project teams to develop validation strategy and statistically sound tests for appropriate support of results.
Complete test method validation, gauges R&R studies and other qualifications or studies to support product testing.
Scheduling coordination, material allocation and alignment of personnel in order to successfully complete validation assignments.
Develop statistically based sampling plans for in-process and final test sequencing.
Ensure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements.
Support and address comments and suggestions associated with validation and engineering documentation.
Protocol, Deviation, and summary report generation and approval.
Change control, non-conformance and CAPA support.
Your profile:
Bachelor's Degree in Engineering (Biomedical, mechanical, chemical, or electrical) or Science (Biology, Chemistry).
2 to 5 years of experience in a Validation or Quality Assurance role for a medical device or pharmaceutical environment.
Fluency in French and good command of English
Demonstrates excellent organizational and communication skills.
Experience with qualifying medical devices, manufacturing equipment or external components.
Excellent technical writing skills with a thorough understanding of good documentation practice.
Competent in tracking and updating schedules to provide upper management visibility of milestones and achievements.
Use of Microsoft office tools
Knowledges of statistical techniques
We are currently seeking a Validation engineer for one of our clients in Canton of Neuchatel.
If you are looking to work in a dynamic and very friendly working environment then this is for you.
This is an open-ended temporary contract
Please note this vacancy requires fluency in French.
Your responsibilities:
Generation and execution of qualification/validation protocols including the generation, routing and approval of summary documentation.
Work with project teams to develop validation strategy and statistically sound tests for appropriate support of results.
Complete test method validation, gauges R&R studies and other qualifications or studies to support product testing.
Scheduling coordination, material allocation and alignment of personnel in order to successfully complete validation assignments.
Develop statistically based sampling plans for in-process and final test sequencing.
Ensure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements.
Support and address comments and suggestions associated with validation and engineering documentation.
Protocol, Deviation, and summary report generation and approval.
Change control, non-conformance and CAPA support.
Your profile:
Bachelor's Degree in Engineering (Biomedical, mechanical, chemical, or electrical) or Science (Biology, Chemistry).
2 to 5 years of experience in a Validation or Quality Assurance role for a medical device or pharmaceutical environment.
Fluency in French and good command of English
Demonstrates excellent organizational and communication skills.
Experience with qualifying medical devices, manufacturing equipment or external components.
Excellent technical writing skills with a thorough understanding of good documentation practice.
Competent in tracking and updating schedules to provide upper management visibility of milestones and achievements.
Use of Microsoft office tools
Knowledges of statistical techniques
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Découvre comment se déroule la procédure de candidature et comment nous pouvons t'aider à trouver un emploi.
Postuler avec nous, c'est facile. Nous examinerons ta candidature et verrons si tu corresponds au poste et à l'entreprise.
Notre consultant t'appellera au moment qui te convient pour discuter de ta candidature et de tes aspirations professionnelles.
Si tu n'as jamais travaillé avec nous auparavant, nous aurons besoin d'informations de base supplémentaires pour confirmer ton éligibilité à travailler en Suisse.
Ensuite, nous devrons simplement vérifier quelques éléments – nous effectuerons les contrôles de conformité appropriés et te tiendrons informé.
Notre équipe d'experts organisera un entretien pour le poste pour lequel tu as postulé ou, si elle pense qu'il existe une meilleure opportunité, elle te proposera également des options alternatives.
Nous veillerons à ce que tu sois parfaitement préparé avant ton entretien et que tu saches exactement à quoi t'attendre – bonne chance!
Félicitations, tu es prêt à commencer ton nouvel emploi. L'équipe veillera à ce que tu sois parfaitement préparé pour ton premier jour.
Après avoir commencé ta nouvelle mission, nous te contacterons pour avoir de tes nouvelles et t'apporter notre soutien dans ton nouveau rôle.
Nous te tiendrons informé lorsque nous aurons des offres d'emploi similaires.
Merci de t'être abonné à tes alertes emploi personnalisées.