Processes: Manage all final product manufacturers (local and via the regional office), final product release Licenses and Site Master Files in place. Manage the local GMP Audit program and conduct external audits and Always apply Risk Management principles in the QA department and adhere to all risk management processes. quality related activities. Represent the Quality Department as part of a cross functional team to ensure Act as the local VEEVA Administrator for South Africa and arrange training for all local users. Ensure
Processes: Manage all final product manufacturers (local and via the regional office), final product release Licenses and Site Master Files in place. Manage the local GMP Audit program and conduct external audits and Always apply Risk Management principles in the QA department and adhere to all risk management processes. quality related activities. Represent the Quality Department as part of a cross functional team to ensure Act as the local VEEVA Administrator for South Africa and arrange training for all local users. Ensure
provide superior Regulatory services to relevant departments within the company and with external Partners with internal product queries from relevant departments Assisting with external product queries from
with internal product queries from relevant departments Effectively managing activity within Regulatory
manage a Pharmacoviligance system compliant to local health authorities and the Company's global requirements
manage a Pharmacoviligance system compliant to local health authorities and the Company's global requirements