Coordination and management of all Quality Assurance (QA) submission functions required by Customers of Online, form based, systemic or questionnaire type formats.
Oversee the compilation and submission of the sample evaluation systems, drug registrations, cosmetic registrations and permitting.
Coordinates with R& D [publications and development to update specifications and to perform submission for new product launches
Coordinates with Contract Manufacturers to gather required technical information, publications and development data to update specifications and to perform submissions for new product launches.
Perform drug product registrations
Submit permit applications and pesticide registrations
Ensure compliance with conditions as laid down by regulatory bodies where appropriate.
Conduct on a periodical basis quality audits and third party vendors and participate in local audits as part of continuously improving the Quality System
Promote and establish collaborations with institutions locally and aboard that with us to develop, manufacture and import products.
Coordinate External Audits for third party manufacturers
Prepare and review written technical reports. Write reports, summaries, and protocols regarding submissions, claims and investigations.
Skills and Requirements
Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed