Beschleunige die Bewerbung, indem du dein Profil teilst
Job Details
For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).
Your role:
Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)
Support Equipment and Automated Systems deviation management.
Support, review and approve change control proposal (CCP) as QA engineering for projects
Participate to risk assessments
Review and approve quality documents (design documents, validation plans & summary reports, procedures, protocols, data reviews, reports and procedural documents)
Ensure that validation, calibration and preventive maintenance programs are in place and are respected
Routine activities:
Review and approve quality documents (operational documents, procedures, forms, intervention report for automation activities) for equipment and automated systems activities
Ensure support for deviations related to equipment and automated systems including QA assessment, investigation and CAPA review / approval and closure
Ensure that periodical technical interventions programs are in place and respected.
Participate to annual reviews as required.
Ensure QA activities in SAP-PM system: equipment/system and maintenance plans creation /modification/removal
Support department to guarantee that equipment and automated systems procedures and forms are understandable and easy to complete and review.
Participate to seminars and training sessions on equipment and automated systems qualifications best practices to maintain "state-of-the-art" in-house expertise.
Ensure backup of the QA engineer for project and routine activities
For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).
Your role:
Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)
Support Equipment and Automated Systems deviation management.
Support, review and approve change control proposal (CCP) as QA engineering for projects
Participate to risk assessments
Review and approve quality documents (design documents, validation plans & summary reports, procedures, protocols, data reviews, reports and procedural documents)
Ensure that validation, calibration and preventive maintenance programs are in place and are respected
Routine activities:
Review and approve quality documents (operational documents, procedures, forms, intervention report for automation activities) for equipment and automated systems activities
Ensure support for deviations related to equipment and automated systems including QA assessment, investigation and CAPA review / approval and closure
Ensure that periodical technical interventions programs are in place and respected.
Participate to annual reviews as required.
Ensure QA activities in SAP-PM system: equipment/system and maintenance plans creation /modification/removal
Support department to guarantee that equipment and automated systems procedures and forms are understandable and easy to complete and review.
Participate to seminars and training sessions on equipment and automated systems qualifications best practices to maintain "state-of-the-art" in-house expertise.
Ensure backup of the QA engineer for project and routine activities
Erfahre wie der Bewerbungsprozess aussieht. Finde heraus wie wir dir helfen werden, diesen Job zu bekommen.
1 von 8
mit randstad bewerben.
Wir werden deine Bewerbung überprüfen und sehen, ob du zu diesem Job und Unternehmen passt.
2 von 8
Wir werden dich kontaktieren.
Unser Consultant wird dich zu einer passenden Zeit anrufen und mit dir deine Bewerbung und deine Karriereziele besprechen.
3 von 8
deine registrierung.
Falls du noch nie mit uns zusammengearbeitet hast, brauchen wir ein paar Informationen um herauszufinden, ob du in der Schweiz arbeitsberechtigt bist.
4 von 8
background check.
Um sicherzustellen, dass du der perfekte Kandidat für diese Rolle bist, werden wir alle relevanten, von dir zur Verfügung gestellten Referenzen kontaktieren.
5 von 8
der perfekte job für dich.
Unser Expertenteam wird entweder ein Vorstellungsgespräch für die Stelle arrangieren, auf die du dich beworben hast oder passende alternativen vorschlagen.
6 von 8
das interview.
Wir werden sicherstellen, dass du vollständig für dein Interview vorbereitet bist und weisst, was dich erwartet. Viel Glück!
7 von 8
dein start im neuen job.
Gratulation! Du bist bereit für deinen neuen Job. Unser Team wird sicherstellen, dass du vollständig vorbereitet für deinen ersten Arbeitstag bist.
8 von 8
beginne deinen neuen job.
Nachdem du deine neue Herausforderung begonnen hast, werden wir dich kontaktieren und sehen, wie es dir geht und wie wir dich in deiner neuen Rolle unterstützen können.
Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· Collabo
Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· Collabo
finde ähnliche Jobs
Wir informieren dich über ähnliche Jobs.
Danke für die Anmeldung zu persönlichen Job-Benachrichtigungen.