Qrm Data Verification Quality Manager
vor 2 Monaten
Quality Risk Management records are migrated from a legacy system to a new system. The migration is quite challenging and requires a 100% manual check of the migrated data including potential correction, also known as data verification. Further the risk records need to be updated according to the project plan to reflect the current situation. Aim of this position is to perform the verification and correction of the migrated risk records in the new system in collaboration with quality management and other functions as required and to perform updates of the risk records. All tasks are conducted with close contact to Data Verification Assistance, QRM Owner and other stakeholders.
Aufgaben
- Data Verification between legacy system and new One QMS (Veeva QRM) - Approvals of documents in consideration of regulatory requirements as well as internal Pharma Quality Standards (PQS) and ensuring the compliance of these.
- Close communication with risk record owner, SMEs and other stakeholders - QA-Approval of verified and/or updated risk records as Quality Assurance - Ensure compliance of approved records with internal and external standards and specification - QA-role as well as owner role für unplanned events
Qualifikation
Technical or university degree (Masters degree ongoing is an option)
- Min. 1-3 years experience as QA Manager in pharmaceutical industry \*\*\*\*\*
- Min. first experience in data verification or data handling \*\*\*\*\*
- First experience in Risk Management \*\*\*\*\* - Common office software (e.g. Google, Microsoft), good understanding of Excel/GSheet, database handling \*\*\*\*\*
- Fluent in German, English min. B2
- Accurate and solution-oriented working, teamplayer
Wir freuen uns auf Ihre vollständige Bewerbung.
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