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Smart4Sciences are currently working with a Pharmaceutical Company in the north of England to recruit a Qualified Person responsible for sign off and release of finished Pharmaceutical products
As a QP you will be responsible for reviewing and evaluating batch records and performing batch certification and release of solid-dose products in accordance with GMP and the Human Medicines Regulations.
Key Responsibilities
- Performing QP batch certification of licensed medicines (per applicable regulations) and providing QP support as required for Quality issues.
- To act as 'Qualified Person' in approving Finished Product for release onto the marketplace.
- Verify and ensure that the products are manufactured, packed and tested to the requirements of registered MA.
- Responsible as named QP on the site MIA. To coordinate the preparation and hosting of MHRA and customer inspections.
Key Requirements
- Eligible to act as Qualified person in UK. Strong understanding of small molecule manufacturing with direct experience in solid oral dosage forms.
- Extensive Pharmaceutical Industry with hands on experience in development/quality in a GxP environment. Knowledge and understanding of drug development process and the Global Regulatory Requirements and regulations related to GxP.
- Excellent working knowledge of EU GMPs, especially in the interpretation of requirements and guidance for the development, manufacture, control, and distribution of commercial product.
This Qualified Person vacancy is an urgent requirement with interviews happening now - if you would be interested please apply today
