An exciting opportunity has arisen for a quality assurance professional within my client's compliance department. The successful candidate will:
Carry out audits according to internal schedule and external vendors as requested.
Administer company change control and corrective/preventative action systems on the site.
Perform compliance reviews on Standard Operating Procedures and Technical Reports.
Review chart recorder traces.
Write and review Standard Operating Procedures and associated documentation including Compliance Reviews of all documentation.
The successful candidate will also be required to support batch release activities and must be flexible in their working hours, as overtime maybe requested.
You must be qualified to at least degree level in a life science, pharmaceutical engineering or Chemistry and have a minimum of one year's pharmaceutical experience. Report writing ability is essential and experience of ISO 9000 auditing is preferred.
To apply, call quoting reference JC103
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