Description
You will be involved in supporting the daily QA activities and ensuring compliance in accordance with cGMP.Some responsibilities include:
- Perform critical or constructive review of documentation and practices.
- Critical and constructive review of investigation reports.
- Effective coordination and communication of adherence to schedules.
- Co - ordinate and participate in internal audits and key quality initiatives as appropriate.
- Work with relevant departments to ensure timely closure of quality actions/findings.
- Measure and report RFT data and work with departments to resolve recurring issues.
- Actively contribute to continuous improvement initiatives.
Candidates must have the following skills and experience:
- Degree or science related qualification.
- Experience working within a Biotech organisation.
- Minimum of 5 years experience in similar role.
- CAPA's, deviations, change controls, non conformances and similar activities.
- Proven experience in report writing and technical writing.
This is an excellent opportunity for work with a leading company.
The client requires experience in the areas above to be clearly stated on your CV and have requested a brief paragraph from each candidate providing the reasons they are good for this role.
If you would like to apply please contact Sarah Irvine on or respond to this advert.