One of our valued pharmaceutical clients is looking for a QA professional to join their Quality Department in Cambridge on a full time on-site basis.

This organisation has been researching, developing and supplying novel, effective and popular dermatological treatments for the NHS and OTC use for over half a century and are one of the most successful marketeers in the UK.

What you will be doing:

Provide support to the Quality Assurance Manager / Responsible Person as directed.
Assist in implementation/maintenance of GxP cross-company QA processes.
Updating and maintaining WDA(H) documentation.
Create and update GDP and Quality related processes and documentation.
Provide support with the Supplier Quality Incident process.
Support with the Deviation/CAPA process.
Maintain and distribute Supplier related documentation as requested.
Perform Internal Audits and Reports and support external supplier audits, when required.
What makes you a good fit:

Quality experience in a pharmaceutical environment along with a degree (or equivalent) in a relevant scientific discipline is desirable.
Clear understanding of; GDP/GMP, or any other GxP area, regulatory and accreditation systems, and quality management.
Excellent analytical thinking skills.
Excellent interpersonal skills.
Ability to analyse information and prepare coherent investigative/technical reports.
Competence in computer packages including Microsoft Office and electronic quality management packages.
Competence in preparing presentations, delivering training to a variety of internal audiences.
Ability to plan, organise and manage multiple projects.
Excellent attention to detail and documentation skills.
If you're an ambitious quality professional with good exposure to Quality in GMP/GDP settings and interested in exploring new opportunities, please send us through an updated resume, or contact Freya Peniston-Bird directly on (phone number removed) to hear more