Description
You will be involved in supporting the daily QA activities and ensuring compliance in accordance with cGMP.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.
- Coordinate 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 data and work with departments to resolve issues.
- Actively contribute to continuous improvement initiatives.
Candidates must have the following skills and experience:
- Degree or science related qualification
- 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 exciting opportunity with competitive hourly rates. If you would like to apply please contact Sarah Irvine on or submit a copy of your current CV.
We also offer shopping vouchers for an successful referrals, so if you know of anyone who may be looking please feel free to get in touch.