Candidates Specifications: Experience in CAPA and SOP management in PV Educational Qualification / Certification Any Graduates Job Description:
3+ Years of experience in CAPA and SOP management in Pharmacovigilance Domain
To collaborate with various client departments/teams and ensure proper development of CAPAs & Deviations from internal quality audits. To also support in providing oversight and ensure proper.
development of documentation during regulatory inspections.
To support in the development of responses to Audit Regulatory Inspections and/or
Process Deviation observations.
To organize and coordinate required meetings with external and internal key stakeholders to
expedite CAPA preparation and closure process.
To ensure timely and effective closure of assigned global PV CAPAs & Deviations.
To contribute to PV CAPA implementation and documentation by completing all required processes.
Create and publish periodic compliance dashboards with stakeholders in agreed formats.
Employement Category:
Employement Type: Full timeIndustry: Bio Technology & Life SciencesFunctional Area: PharmaceuticalRole Category: Quality Control ManagerRole/Responsibilies: Capa Management