Qualified Person (QP)

RBW Consulting; Nottingham; On-site; GBP 40,000 - 60,000; Full time

Job summary

A global pharmaceutical organization is seeking an experienced Qualified Person (QP) to join their Nottingham team. In this permanent role, you will ensure compliance with GMP standards and certify batches for market release. The ideal candidate will have current eligibility as a Qualified Person and strong knowledge of pharmaceutical quality systems. This position offers a competitive salary, comprehensive benefits, and opportunities for professional development within a collaborative environment focused on quality and innovation.

Benefits

Competitive salary

Comprehensive benefits package

Professional development opportunities

Qualifications

• Current eligibility and registration as a Qualified Person under UK/EU law.
• Strong knowledge of GMP and pharmaceutical quality systems.
• Experience within sterile pharmaceutical manufacturing is highly desirable.

Responsibilities

• Act as a Qualified Person ensuring compliance with GMP standards.
• Certify batches for release to market, maintaining product quality.
• Provide guidance on quality systems and regulatory compliance.

Skills

Knowledge of GMP

Problem-solving skills

Communication skills

Education

Eligibility as Qualified Person under UK/EU law

Job description

Qualified Person (QP)

Location: Nottingham
Employment Type: Permanent, Full-Time
Company: Global Pharmaceutical Organization

We are looking for an experienced Qualified Person (QP) to join a Nottingham-based team on a permanent basis. This is an exciting opportunity to work with a global pharmaceutical company that offers a strong benefits package and a collaborative environment focused on quality and innovation.

Key Responsibilities

• Act as a Qualified Person in accordance with EU and UK regulations, ensuring compliance with GMP standards.
• Certify batches for release to market, maintaining the highest standards of product quality and patient safety.
• Provide expert guidance on quality systems, regulatory compliance, and continuous improvement initiatives.
• Collaborate with cross-functional teams to support manufacturing and supply chain operations.
• Contribute to audits and inspections, ensuring readiness and compliance at all times.

Requirements

• Current eligibility and registration as a Qualified Person under UK/EU law.
• Strong knowledge of GMP and pharmaceutical quality systems.
• Experience within sterile pharmaceutical manufacturing is highly desirable.
• Excellent communication and problem-solving skills.
• Ability to work effectively in a global, fast-paced environment.

What’s on Offer

• Competitive salary and comprehensive benefits package.
• Permanent position within a global organization committed to quality and innovation.
• Opportunities for professional development and career progression.

Ready to take the next step?

Apply today and become part of a global team dedicated to improving patient outcomes worldwide.