The Opportunity:

This is an opportunity to be part of a dynamic team within the quality function. We are looking for individuals who will support and drive Chanelle Pharma’s vision to be the most valued global provider of high quality, competitively priced pharmaceutical products and to provide excellent services and support to our customers.

In this role you will report into QA Supervisor

KEY RESPONSIBILITIES:

· To carry out finished goods inspection for all products manufactured and packaged by Chanelle prior to product release and shipment.

· For all externally manufactured / packed products for which are released by Chanelle to carry out documentation review and inspect supplied samples prior to product release and shipment.

· Generation of Certificate of Analysis / Certificate of Conformance.

· Approval of Shelf life’s on Packaging Work Orders.

· To follow through on any corrective actions on deviations raised against batches.

· For all products manufactured and/or packaged by Chanelle to ensure that sufficient retains are stored and organized in such a way that allows them to be easily accessed.

· To ensure that all batch documentation is filed and stored in such a way that any batch can be easily accessed.

· Scanning of all Batch documents as required.

· To carry out GMP walks as required.

· To assist with the writing and updating of QA procedures as appropriate.

· To ensure timely feedback on queries both internal and external.

· To provide Data loggers to warehouse as required for products been dispatched.

· To attend morning meetings at the Visual Board and update Shipping Schedule and End of Line file.

· To attend any meetings which are deemed necessary.

· To attend the production morning meetings and to action any tasks for Quality.

· To collect all in-house work orders from production and delegate these to all QA Inspectors for batch review.

· Time Management System

· To carry out duties as may be assigned by the Quality Supervisor / Manager.

COMPETENCIES:

· Quality/Compliance

· Customer Focused

· Communication

· Collegiality

· Initiative

· Efficiency

· Teamwork

· Responsibility

· Commercial Awareness

· Decision Making

QUALIFICATIONS:

· Previous experience in a pharmaceutical / manufacturing environment essential.

· 2+ years’ experience in Quality Assurance / Documentation desirable.

· Preferred Science qualification

· Excellent attention to detail required.

· Good IT & Business Administration Skills.