Adcock Ingram is a leading South African pharmaceutical company with a proud 130 year heritage. It has a portfolio of trusted, quality brands and generics and an entrenched value system that assures integrity. Growing from humble beginnings as a small Krugersdorp pharmacy in 1890, Adcock’s portfolio includes an extensive range of Prescription, Over-the-co...
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Pharmacy Bachelor’s degree or equivalent in life sciences or technology-related discipline with minimum 2 years Regulatory Operations experience required.
OR
Grade 12 with at least 5 years pharmaceutical industry experience, with prior Regulatory Operations experience required.
Experience leading the management of projects/timelines and collaborating with team members
Expertise in the use of a document management, eCTD format and regulatory submission requirements and eCTD publishing systems
Advanced technical skills in best business practices for electronic regulatory document preparation and submission, and document and life cycle management systems
Previous experience developing work instructions and generating SOP’s that are consistent with health authority requirements and company business practices
Proven ability to manage, streamline and collaborate to improve document preparation and management systems
Key Job Outputs
Responsible for overseeing and guiding the operations of teams managing the creation, assembly, and publishing of electronic submissions, including New Product Applications and Life Cycle Amendments.
Represents Regulatory Operations on project teams for matters relating to electronic submissions, driving timelines and deliverables related to submission documents.
Maintain working knowledge of the regulations and processes that govern the content and maintenance of controlled documents required by the Health Authorities, ICH and internal working practices.
Liaise with functional source areas (clinical, quality, regulatory) to ensure documents are compliant with authoring style guide. Work with regulatory document authors to achieve resolution and ensure that documents comply with regulatory and company guidance/template specifications.
Supports and/or leads the development, refinement, and implementation of internal processes, procedures, work instructions and training programs for submission production and operational support activities to the RA Systems Department. As needed, trains colleagues and project teams.
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