Tashida Pharma is recruiting for a (Senior) Auditor specialising in GCP Clinical Trials to ensure compliance with SOPs, regulations, and guidelines.
This permanent role involves conducting internal audits of processes, QMS, facilities, and external audits (vendors, etc.).
Responsibilities:
Maintaining compliance Leading internal and external audits QMS review and management
Qualifications: Strong GCP auditing experience Knowledge of drug development Understanding of regulatory standards in pharmaceutical or clinical settings A degree in Science or equivalent is desirable
This is a hybrid role which consists of three days a week in the office (London) and two days from home. #J-18808-Ljbffr
This permanent role involves conducting internal audits of processes, QMS, facilities, and external audits (vendors, etc.).
Responsibilities:
Maintaining compliance Leading internal and external audits QMS review and management
Qualifications: Strong GCP auditing experience Knowledge of drug development Understanding of regulatory standards in pharmaceutical or clinical settings A degree in Science or equivalent is desirable
This is a hybrid role which consists of three days a week in the office (London) and two days from home. #J-18808-Ljbffr
