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Qualified Person (QP) - Sterile Manufacturing

Are you a Qualified Person with experience in sterile pharmaceutical manufacturing? Looking to make an impact in a forward-thinking company where quality and patient safety come first?

Smart4 Sciences are working with a pharmaceutical manufacturer in Essex specialising in the production of sterile and non-sterile products. As part of their continued expansion, they're seeking an experienced and proactive Qualified Person to join their quality team.

The Role:

As a QP, you'll be responsible for ensuring that products released to market meet the highest standards of GMP compliance and patient safety. Working in a modern GMP facility, you will:

Act as a QP for the certification and release of sterile pharmaceutical products

Ensure full compliance with MHRA and EU GMP guidelines

Liaise closely with QA, Production, and Regulatory Affairs teams

Contribute to audits, inspections, and continuous improvement projects

Support the development of junior QA staff and provide QP oversight where needed

About You:

Eligible to act as a Qualified Person under Directive 2001/83/EC

Prior experience working with sterile manufacturing (aseptic/terminally sterilised products) is desirable

Strong working knowledge of EU GMP and UK pharmaceutical regulations

If you're a QP ready for your next challenge in a state-of-the-art sterile manufacturing environment, we'd love to hear from you!

Apply today or contact Gareth Gooley on for a confidential discussion.

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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

Read less

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

Read less