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Internal Audit Legacy Reviewer
Eingestellt von Edelway
Gesuchte Skills: Client
Projektbeschreibung
Internal Audit Legacy Reviewer
Our global multinational end client in the Bern/Basel (Pharmaceuticals/Medical Devices) area is currently looking for an Internal Audit Legacy Reviewer to join them on a long term basis.
Working Language: German. English is a plus.
THE ROLE
* Reviewing internal and provide audit reports and supporting documentation against pre-approved checklists
* Review training records to ensure completeness against a pre-approved checklist
* Note any identified deficiencies
* Assign remediation levels
* Coordinate review process with project coordinator (US Based individual)
* Facilitate any necessary remediation activities with local site representative.
* Assure adherence to all documentation practice standards.
* Escalate any issues/delays immediately.
YOUR PROFILE
* Experience within the medical device industry, specifically facilitating and performing internal audits and facilitating all corrective action follow ups.
* Experience within CAPA (Corrective and Preventive Action) systems, both as an approver and action/task owner.
* High level of proficiency in MS Word and Excel.
* Experience on remediation project a plus.
* Demonstrated excellent written and verbal communication skills.
* German fluency required.
Our global multinational end client in the Bern/Basel (Pharmaceuticals/Medical Devices) area is currently looking for an Internal Audit Legacy Reviewer to join them on a long term basis.
Working Language: German. English is a plus.
THE ROLE
* Reviewing internal and provide audit reports and supporting documentation against pre-approved checklists
* Review training records to ensure completeness against a pre-approved checklist
* Note any identified deficiencies
* Assign remediation levels
* Coordinate review process with project coordinator (US Based individual)
* Facilitate any necessary remediation activities with local site representative.
* Assure adherence to all documentation practice standards.
* Escalate any issues/delays immediately.
YOUR PROFILE
* Experience within the medical device industry, specifically facilitating and performing internal audits and facilitating all corrective action follow ups.
* Experience within CAPA (Corrective and Preventive Action) systems, both as an approver and action/task owner.
* High level of proficiency in MS Word and Excel.
* Experience on remediation project a plus.
* Demonstrated excellent written and verbal communication skills.
* German fluency required.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung