training:
Required experience:
Desirable
compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines applications for submission to the regulatory authorities Work in collaboration with internal and external maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate
team
Approving, maintaining, and accurately capturing and authorizing any changes to manufacturing master formulas formulas for release. Liaising with independent authorities and overseas technology providers regarding external
Africa cluster and as required by Marketing Authorization Holders (MAH) and/or study sponsors, as applicable relationships within the organization and with authorities. Ability to manage multiple critical issues and
Africa cluster and as required by Marketing Authorization Holders (MAH) and/or study sponsors, as applicable relationships within the organization and with authorities. Ability to manage multiple critical issues and
databases are corrected, initialed and dated by the authorized signatory
as main subjects DUTIES, RESPONSIBILITIES AND AUTHORITIES ADMINISTRATION – aspects in seed health testing