To operate pharmaceutical plant to manufacture bulk pharmaceuticals, intermediates and other chemical products in accordance with current good manufacturing practice (cGMP) and Health and safety practices.
Principal accountabilities
To perform chemical reactions according to batch sheet and process instructions as requested.
To recognise key reaction criteria and notify a Supervisor or Shift Manager of any unusual signs.
An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department.
In this role you will be responsible to deliver end to end regulatory package under ODM-Distributor scheme in compliance with established quality management system, overseeing (but not limited to) initial compilation of design control evidences, supplier management, incoming inspection and product release process, product submission, post-market surveillance, vigilance and associated reporting.