POSITION OVERVIEW:

Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent’s advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents , ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start here

• Create and revise Master Batch Production Record documents and specification sheets, for pharmaceutical products. Maintains revision records for changes to products. Logs, obtain approvals and tracks progress on master document related change requests;
• Produces new master gel and colorant documents based on drafts submitted by Pharmaceutical Sciences;
• Produces softgel specification sheets for new products;
• Maintains MBPR packages and ensures all are up to date and ready according to planning schedule. Keeps appropriate records archived for required retention time.
• Assists in the creation and revision of SOP’s, specification sheets, and ACF’s/REF’s as per change requests;
• Supports the site administrator by initiating change control forms. Routes for approvals and maintains log in change control system. Closes and files completed change control forms.