We are working on behalf of our client who is a leading manufacturer of scientific instruments for a wide range of applications in the clinical, life sciences and industrial markets. They are looking to recruit an Interim Regulatory/Quality Professional who can provide a first class holistic service in order to prepare them for an upcoming audit.
Role Purpose:
The successful candidate needs to be experienced within the Medical Device sector with a sound knowledge and recent experience of preparing for a Medical Device Single Audit Program (MDSAP).
The ability to be able to review all current processes, systems and existing QMS is essential, along with the experience of devising and executing plans to improve where necessary.
Requirements include:
• A sound knowledge of MDSAP and recent of experience of preparing for this.
• Recent audit experience – preparing and hosting for these are desirable.
• Experience of reviewing all existing processes, devising and implementing new plans.
• Experience of working with companies that supply into the US and Canada.
Location:
Cambridge, UK
Duration and days per week:
3-6 months, 4 -5 days per week.
Keywords:
MDSAP, FDA, Audit, Medical Device, GAP Analysis, QMS, Quality, Regulatory, Scientific Instruments, US, Canada, Medical Device Single Audit Program
To register your interest in this opportunity please forward an up-to-date CV to resourcing@pir-resourcing.com or contact Emma Julian on 01480 499580, quoting reference 882546 and advising current availability and anticipated day rate.