We’re looking for an experienced Qualified Person (QP) with a strong background in sterile manufacturing to join a leading UK biopharmaceutical organisation.
This is an opportunity to play a key role in ensuring GMP compliance and the delivery of safe and effective vaccines.
Key Responsibilities:
* Act as a QP, overseeing batch certification for sterile products.
* Lead operational quality initiatives, ensuring inspection readiness and regulatory compliance.
* Provide expert guidance on GMP standards, maintaining the highest levels of product safety and efficacy.
* Take the lead in internal and external audits, ensuring robust quality oversight.
Requirements:
* QP status with extensive sterile manufacturing experience.
* Strong background in operational quality and inspection readiness within GMP environments.
* Proven leadership and stakeholder management skills, driving a culture of collaboration and excellence.
* Ability to be on-site full-time to provide hands-on support.
Why Join?
* Competitive compensation, recognising top industry talent.
* Work on cutting-edge biopharmaceutical products with a high-impact role.
* A supportive, growth-focused environment where your expertise makes a difference.
* UK residency required.
Contact us confidentially to explore this exclusive opportunity.