This is a newly created role reporting to the Head of Quality; you will be responsible for Regulatory Affairs and Quality Assurance activities for a fast-growing company in the Complementary Medicines industry.
Your experience working as part of a team within a rapid paced and deadline driven environment will see you excel in this role.
You will need highly developed attention to detail and research skills to maintain regulatory compliance of all current products.
Your key responsibilities will include:
Developing Evidence Packages and Tables for all new products
Managing Bulk Specifications
Compiling Shelf-Life Justifications
Developing and coordinating recent product labels to meet all regulatory requirements such as TGO92 & 116
Reviewing and submitting Listed Medicines on the ARTG
Maintaining regulatory compliance of all products
Managing Change Control for new products
Managing all Product Stability activities