Quality Assurance Specialist
4 weeks ago
We are seeking a highly skilled and experienced Qualified Person (QP) to join our team at GSK. As a QP, you will play a critical role in ensuring the quality and compliance of our products, from manufacturing to release.
Key Responsibilities- Review and certify finished products for release, ensuring compliance with regulatory requirements and GMP standards.
- Collaborate with cross-functional teams to identify and implement quality improvements and process enhancements.
- Develop and maintain quality documentation, including SOPs, technical reports, and deviation reports.
- Provide oversight of change-control, complaint, distribution, self-inspection, and other key processes within the Quality Management System.
- Deputise for Quality Managers in the completion of QA approval of key site documents.
To be successful in this role, you will need to be a Qualified Person (QP) with a recognized qualification in the UK. You will also have a strong background in quality assurance, with experience working in a sophisticated manufacturing site. You will be self-motivated, with excellent communication skills and the ability to work effectively in a team environment.
About GSKGSK is a global biopharma company with a special purpose – to unite science, technology, and talent to get ahead of disease together. We prevent and treat disease with vaccines, specialty, and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas: infectious diseases, HIV, respiratory/immunology, and oncology.
What We OfferWe offer a competitive base salary, annual bonus based on company performance, opportunities for on-the-job training, and access to industry conferences. We also offer opportunities for support for professional development and chartership, as well as employee recognition programs and hybrid working arrangements.
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