Qualified Person

ROLE OVERVIEW

We are currently looking for a Qualified Person to join a leading pharmaceutical contract development and manufacturing organisation based in the South East of the UK. This is an exciting opportunity for an experienced QP professional to make a direct impact on bringing complex, life-changing medicines to market within a collaborative and supportive environment.

As a key member of the quality team, you will ensure the compliant certification and release of finished pharmaceutical products, helping to uphold the highest industry standards and contribute to innovative healthcare solutions.

KEY DUTIES AND RESPONSIBILITIES

Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:

    • Act as the Qualified Person to certify and release finished medicinal products, ensuring compliance with GMP and regulatory requirements.

    • Collaborate closely with the Head of Quality on significant quality issues and maintain shared responsibility for batch certification.

    • Review and approve non-conformance reports (NCRs & LIRs) to support continuous improvement.

    • Provide GMP advice and guidance across various departments within the business.

    • As the Qualified Person, you will mentor quality colleagues and support the development of Trainee QPs.

ROLE REQUIREMENTS

To be successful in your application to this exciting role as the Qualified Person we are looking to identify the following on your profile and past history:

    • A Degree or higher level in a relevant field (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).

    • Proven experience as a Qualified Person within a licensed pharmaceutical manufacturing environment, preferably with experience in oral solid dosage forms and highly potent drugs.

    • Extensive knowledge of GMP regulations and certification processes for medicinal products.

Key Words: Qualified Person / Pharmaceutical Manufacturing / GMP / Quality Assurance / Certifications / Medicinal Products / CDMO / Oral Solid Dosage Forms / Regulatory Compliance / Healthcare / Pharmaceutical Industry

"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career