Description
A Global Pharmaceutical organisation currently requires a QC Validation Engineer to join their team. The purpose of the role is to provide technical leadership and to co-ordinate the activities of validation work within quality control function.The Role:
*To work within compliance, in respect to validation activities on matters of procedural documentation, change control, quality systems, equipment verification and business improvements.
*To provide support to check and verify that the work conducted in the department is to the highest standard and is tested in an efficient manner to meet customer needs.
*Provide validation support to all areas within the Quality Control departments to ensure equipment is validated as required.
*Write and execute validation protocols.
*Review data generated from validation activities.
*Monitor ongoing validation exercises and provide regular updates on progress.
Experience Required
*Strong cGMP background in the Biological or Pharmaceutical industry.
*Strong back ground in equipment validation including thermal equipment and laboratory instrumentation.
*Strong background in working with 21 CFR part 11.
*Experience of QC testing.
*Experience in sterile manufacturing and testing.
A fantastic hourly rate is on offer alongside an exceptional opportunity to join a major pharmaceutical organisation.
Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this opportunity.