Contract: Full Time.
Salary: Competitive (dependent on experience).
Maintaining of QMS and implementing new strategies where necessary
Monitoring, reporting and auditing of clinical trials
Ensuring design control standards are in line with EU regulations (IEC 62304/ ISO
Hosting of internal inspections asides Notified Body Audits
Providing expert regulatory and compliance advice to researchers
Minimum of 3 years’ experience in a Quality/Regulatory position
Knowledge of safety risk management (ISO 14971)
Knowledge of SAS and CDISC
I am looking forward to having a chat with you if you are suitable for this role. For more
information on this exciting opportunity please email a copy of your CV in MS WORD format to
firstname.lastname@example.org using Quality Assurance Manager as the Subject.
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