Job Description
As a Biopharmaceutical Compliance Specialist at CK Group, you will play a key role in supporting the HPQE in GCSO quality and compliance infrastructure development.
You will work closely with Global Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) GCP, GLP, PV and relevant local and international regulations.
This position requires experience writing SOPs and using Veeva Systems.