What we are looking for: A Global Technical Product Manager.
What you
qualifying and closing the deal. (National/ Regional and Global) Prepare tenders, reports, presentations, Approve
Title: Global Talent Acquisition Manager
Department: Global People/HR Function
Location/Branch: responsible for: Global Talent Acquisition Team (India, SA and China)
Our client is a global provider of private sector internationally.
The role of Global Talent Acquisition Manager is crucial in ensuring and aligned with organizational goals.
The Global Talent Acquisition is responsible for establishing constant presence externally, attracting top talent globally, ensuring the organization becomes and remains
Resolve is seeking a Global Procurement Energy Sourcing Specialist for our client, a global leader in the Beverages experience in energy sourcing and a desire to work in a global procurement environment, we encourage you to consider logisticshireresolve.za.com When applying via email please use "Global Procurement Energy Sourcing Specialist" as your
JOB PURPOSE
The Process Owner - Record to Report owns the end-to-end process design and drive change initiatives related to system, process and policy, including involvement in the delivery of the change initiatives as part of a transformation program and a steady state Business As Usual (B
Leader A Fortune 500 Company that specialises in Global Logistics.
Minimum requirements:
reviewing Chemistry, Manufacturing, and Controls (CMC) documentation, and maintaining up-to-date knowledge with project schedules. 2. CMC Writing: Write and review high-quality CMC documentation for regulatory the Common Technical Document (CTD). Ensure that CMC documents are accurate, complete, and compliant with pharmaceutical industry. Demonstrated experience in CMC writing and preparation of regulatory submissions
reviewing Chemistry, Manufacturing, and Controls (CMC) documentation, and maintaining up-to-date knowledge with project schedules. 2. CMC Writing: Write and review high-quality CMC documentation for regulatory the Common Technical Document (CTD). Ensure that CMC documents are accurate, complete, and compliant with pharmaceutical industry. Demonstrated experience in CMC writing and preparation of regulatory submissions
teams.
Applies knowledge of current local and global Regulatory trends to identify future regulatory
/>Responsible for the management of a skill group such as CMC, Regulatory affairs project management, etc.
Contribute effectively to Global Development programmes, providing expert advice
registrations
Ensures effective collaboration across the global, regional and local Regulatory Affairs interface
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for variations (CMC & Labelling), Renewals, Artwork updates etc.