Description
Leading Pharmaceutical manufacturing plant have an URGENT contract requirement for an experienced QA Specialist to lead the quality issues of a de-commissioning/shut down project.The manufacturing aseptic fill/finish facility will be closing down with operational activities to stop in May and the site to close in August so we are looking for an experienced QA Specialist to support the final de-commissioning phases.
To be successful for this role we are looking for a QA Specialist with the following skills and experience:
Role Requirements:
- Aseptic facility experience.
- Must have De-commissioning experience (or commissioning - reverse engineer the process!).
- Authoring deviation reports.
- Managing change controls.
- Writing and executing documents on the QMS.
- Product Risk Assessments.
- Ideally experience within Microbiology Laboratories.
- Validation experience is a bonus.
- QP qualified is a bonus.