A long-establihed leader in the pharmaceutical sector has an opportunity for an experienced regulatory affairs scientist, or senior regulatory affairs associate, to assist their experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory affairs scientist or regula
and as part of a team.
that processes needed for the integrated quality management system is established, implemented, and main Reporting to senior management on the performance of SHEQ System for Management
that processes needed for the integrated quality management system is established, implemented, and maintained senior management on the performance of SHEQ System for Management Reporting to senior management the integrated integrated quality management system and any need for improvement or risk in all departments Conduct
000
Report to : Quality Assurance Manager
Job Overview:
The
Quality Management System
with cross-functional teams including product management, underwriting, and marketing to define product
accepted changes through regulatory compliance. Manage the timing of implementation of change at the contractor proposal of corrective and preventative action. Manage the implementation of any proposed corrective action responsible pharmacist with Afrivet Business management audits by South African regulatory bodies with
accepted changes through regulatory compliance. Manage the timing of implementation of change at the contractor proposal of corrective and preventative action. Manage the implementation of any proposed corrective action responsible pharmacist with Afrivet Business management audits by South African regulatory bodies with
forums, congresses and seminars as recommended by Management. Investigative searches to possibilities of improvement risks. Communicate/recommend possibilities to Management in acquiring approval. LIASON Liaison with suppliers Industry forums and congresses when recommended by Management. SUPERVISORY CAPACITY AND TRAINING Responsible