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dettagli di lavoro
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
qualifiche
Your profile:
English B2 or above
Master / Bac +5 level
Knowledge of equipments and automated systems
Knowledge on Trackwise, CSV and SAP are mandatory
3-5 years of experience in a similar position
Experience in Quality Assurance
Expertise in cGMP best practices
contattaci.
saremo felici di rispondere alle tue domande in merito a questa posizione.
Sai come funziona il nostro iter di selezione? Scopri come aiutiamo le persone a trovare il lavoro giusto.
1 di 8
candidati con Randstad.
Candidarsi alle nostre offerte di lavoro è facile. Dopo aver ricevuto la tua domanda di impiego, la verificheremo per capire se è linea con il ruolo professionale e l’azienda.
2 di 8
ti ricontatteremo.
Il nostro consulente ti contatterà a tempo debito per discutere la tua candidatura e futuri desideri di carriera.
3 di 8
per registrarti.
Se non hai ancora lavorato con noi, avremo bisogno di ulteriori informazioni di base per confermare la tua idoneità a lavorare in Svizzera.
4 di 8
verifica compatibilità, referenze e formazione.
Dovremo poi controllare un paio di dati – faremo le necessarie verifiche di compatibilità per assicurarci che tu sia il candidato ideale per il ruolo, contatteremo le referenze che ci hai trasmesso e ti aggiorneremo.
5 di 8
il lavoro perfetto per te.
Il nostro team di esperti organizzerà un colloquio per il profilo per cui ti sei candidato oppure, in caso di migliori opportunità, ti proporrà delle alternative.
6 di 8
il colloquio.
Ci assicureremo che tu sia perfettamente preparato ad affrontare il tuo colloquio e al corrente di quello che ti aspetta. Buona fortuna!
7 di 8
inizia il tuo nuovo impiego.
Congratulazioni! Sei pronto per iniziare il tuo nuovo impiego. Il team garantirà che tu sia perfettamente pronto ad affrontare il tuo primo giorno di lavoro.
8 di 8
supporto continuo.
Una volta iniziata la tua nuova sfida, ti contatteremo per vedere come procede e per assicurarci che tu abbia il nostro supporto nello svolgimento del tuo impiego.
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
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