GMP Quality Specialist

4 days ago


London, Greater London, United Kingdom Planet Pharma Full time
Global Quality Specialist Opportunity

We are seeking an experienced Quality Assurance professional to join our Global Development Quality group as a Contract Quality Specialist. As a Quality Specialist, your primary duties will include:

Key Responsibilities:
  • Conducting the final review of clinical batch records to ensure compliance with GMP standards and adherence to regulatory filings.
  • Compiling and approving data packs for presentation to the Qualified Person (QP) for final release.
  • Collaborating closely with global teams supporting the clinical supply chain and both internal and external clinical manufacturing sites worldwide.

Previous experience in a QA or similar role within a GMP environment is highly desirable. New science graduates with a Bachelor's degree and a strong willingness to learn are also encouraged to apply. Excellent communication skills and the ability to manage tasks with minimal supervision are essential.

Our client is a global healthcare leader, known for its dedication to improving health and well-being worldwide. With a presence in over 140 countries, focusing on the development and delivery of innovative medicines, vaccines, and healthcare solutions. Employees gain exposure to international projects and opportunities for global career advancement.

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.



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