With the increasing focus on Quality within Takeda, we are now recruiting for a Quality Partner to join the Regulatory Affairs and Quality team.

The successful candidate will be responsible for leading on the implementation of a non-GxP audit and self-inspection programme, supporting the organisation with the implementation of the new procedures for tender and contract management and ensuring the Quality department can better service the increasing variety and volume of Quality needs across the organisation.

We are looking for someone with prior experience of planning and performing audits, working with third party vendors, delivering training and driving compliance through effective monitoring and intervention. Prior experience in a quality related role and/or with a clear understanding of what good Quality Management System comprises and experience of authoring and reviewing policy and procedure documents is required. Knowledge of Pharmacovigilance and Compliance guidelines and requirements would be beneficial. The candidate must be able to demonstrate their ability to drive and deliver results and work effectively cross functionally.

The role will be reporting to the Regulatory Affairs and Quality Manager.

Further skills required for the role:

  • Excellent planning and organisational skills
  • First class communication skills, both in writing and verbally
  • Knowledge of auditing and contract management
  • Strong influencing and negotiation skills with evidence of effective cross functional working, both internally and externally
  • The ability to effectively monitor and track compliance
  • Ability to operate effectively as part of a team and independently

 

To apply please contact our HR consultant, Cally Howarth on 07880 500917 or send your CV to cally@halo-life.co.uk

 

 

Date of Preparation: May 2017

 

Takeda Pharma