Regulatory Affairs Consultant

RRxCo is seeking a Regulatory Affairs Consultant to assist with a 12-month initial project for a leading Medical Device (Medtech) manufacturer to support several activities in the overall program.
The program will based in the United Kingdom, with some onsite presence needed at one of their sites in the Midlands (for the first 6 months, ideally 3 days a week).
You will be responsible for the delivery of the output from several specialists within the regulatory affairs group to ensure department milestones are met.
Requirements 4 - 10 years of Life Science Regulatory Affairs (RA) experience in a Medical Device, Pharmaceutical or Biotechnology setting.
Natural people/project leader.
Past experience of team management.
Past working and interactions with regulatory authorities (MHRA, CQC and BSI).
Ideally both local and global regulatory exposure