Description
Dynamic overseas based biomedical company has an urgent requirement for an experienced Quality Engineer/Specialist to run a variety of remediation projects relating to their Quality Systems Improvement Plan.Working alongside the validation team you will be focussing on quality documentation, technical writing and deviations.
Skills/Experience required:
. Prior experience of audit preparation; PAI/FDA Inspections
. Filling or Fill/Finish experience
. Deviation report writing and handling
. cGMP/FDA knowledge
This 6-12 month contract opportunity will suit an experienced Quality professional who can demonstrate previous experience of PAI readiness.
Please contact - Rebecca Church