Responsible Person RP

3 hours ago


NewcastleunderLyme Staffordshire, United Kingdom SKC Recruitment Full time

Quality Management & GDP Compliance:
Manage all GDP and quality-related activities for the UK business.
Implement and maintain the Quality Management System (QMS) and approve all GDP SOPs/documentation.
Handle all UK quality complaints and collaborate with Global Complaint Management Team.
Ensure compliance for medical devices and cosmetic registration with UK authorities.
Training & Compliance:
Maintain training records and conduct ongoing training sessions.
Provide training to staff and ensure competency in handling pharmaceutical products.
Regulatory Compliance & Documentation:
Manage documentation for product quality, traceability, complaints, returns, recalls, deviations, and CAPA.
Identify areas for process improvement to enhance quality and compliance.
Regularly update the UK Senior Management Team with quality reports and updates.
Decision Making & Risk Management:
Ensure decisions related to product safety and quality do not compromise compliance.
Up-to-date knowledge of GDP legislation and UK regulatory framework.
Ability to work independently, analyze data, assess risks, and propose solutions.
Previous ownership of a QMS and experience within a pharmaceutical manufacturer.
Excellent planning, time management, and problem-solving skills.
Office-based in the Midlands, with potential travel within the UK and internationally.
Flexible working arrangements with 3 days in the office and 2 days from home. UK driving license required.



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