company has a vacancy for a Head of Regulatory Affairs and Responsible Pharmacist. Job Purpose: To describe Quality Assurance/ Pharmacovigilance/ Medical Affairs. Ensure the availability of training plans according according to the training plan. Head of Regulatory Affairs Duties: Ensuring alignment of global and regional commercial strategic plan with the Regulatory affairs submission plans for all markets within the region provide insight into RA activities and report on department progress. Form part of the global Senior Leadership
company has a vacancy for a Head of Regulatory Affairs and Responsible Pharmacist. Job Purpose: To describe Quality Assurance/ Pharmacovigilance/ Medical Affairs. Ensure the availability of training plans according according to the training plan. Head of Regulatory Affairs Duties: Ensuring alignment of global and regional commercial strategic plan with the Regulatory affairs submission plans for all markets within the region provide insight into RA activities and report on department progress. Form part of the global Senior Leadership
Quality Assurance/ Pharmacovigilance/ Medical Affairs. Requirements: Related Bachelor's Degree Minimum
Quality Assurance/ Pharmacovigilance/ Medical Affairs. Requirements: Related Bachelor's Degree Minimum
Quality Assurance/ Pharmacovigilance/ Medical Affairs Qualifying Requirements are: CA(SA) Minimum 5 years
Quality Assurance/ Pharmacovigilance/ Medical Affairs Qualifying Requirements are: CA(SA) Minimum 5 years
Quality Assurance/ Pharmacovigilance/ Medical Affairs Requirements: Related Bachelor's Degree: computer
needed to drive performance in their respective departments. Robust mitigation plans in place to engage. operations of Gazelle through cross-functional departments. Health Authority interactions: All communication proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Candidates
may be an advantage. Experience in regulatory affairs, preferably in human medicines - minimum 8 years
patients ‘needs; Collaborating with the Medical Department to plan and execute educational/scientific activities