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.