product quality vigilance.

DUTIES & RESPONSIBILITIES:

•  Perform end-to-end complaint handling activities, including but not limited to Intake, triaging, recovery of field samples for evaluation, due diligence will be performed with complainant/intake centres/LOCs), trend analysis, defect coding, risk criticality assessment, holistic review and closure of investigations.
• Ensure that uniform and timely management of complaint records from receipt to closure, and investigations are accurately assessed for risk prioritization and performed per procedures, standards and regulations.
•  Compile and analyse data, metrics and trends associated with complaint handling processes.
• Support internal and external audits and inspections; demonstrate ability to communicate regulatory and processpositions as an SME during regulatory inspections.

PROFESSIONAL EXPERIENCE REQUIREMENTS:

• 2-3 years of related experience including Quality Assurance and/or Quality Control, including experience workingin pharmaceutical and/or Medical Device or other related highly regulated industry
• Bachelor’s degree or master’s degree (preferred) in technical, scientific, or engineering disciplines required.
• Global mindset and demonstrated ability for change initiatives, project management and develop strong relationships

La ricerca è rivolta ai candidati ambosessi (L.903/77). Ti preghiamo di leggere l'informativa sulla privacy Randstad (https://www.randstad.it/privacy/) ai sensi dell'art. 13 del Regolamento (UE) 2016/679 sulla protezione dei dati (GDPR).

• Masters or equivalent