Global Quality Assurance Professional
4 days ago
About the Role:
">- As a Global Quality Manager, you will be responsible for planning, executing, and documenting quality-related activities to ensure high standards are met for clinical trial materials, commercial products, and unlicensed medicines.
- You will serve as the Responsible Person and Responsible Person (import) for the UK, managing QA personnel and overseeing quality control for the Manufacturer's 'Specials' Licence.
- The ideal candidate will have extensive knowledge of GMP, GDP, and associated regulations, with a strong background in GMP/GDP environments and at least 5 years' experience in a similar role.
- Key responsibilities include navigating legislative and regulatory requirements for importing and exporting medicines, supporting the NOI process for compliant import of unlicensed medicines into the UK, and guiding on logistical aspects of country regulations related to importing and exporting medicinal products and devices.
Your Profile:
- A university degree in natural sciences or quality management is required, along with business fluency in English and a pragmatic quality mindset with a company-wide perspective.
- We offer an estimated salary range of £60,000 - £80,000 per annum, depending on experience, as well as opportunities for professional growth and development in a global pharmaceutical company.
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