Qualified Person (QP) CV-Library Qualified Person (QP)

Scienceabode; Nottingham; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global pharmaceutical organization in Nottingham seeks a Qualified Person (QP) to ensure compliance with EU and UK regulations. The role offers a competitive salary, comprehensive benefits, and opportunities for professional growth within a collaborative environment. Key responsibilities include certifying product batches, providing guidance on quality systems, and supporting manufacturing operations. Strong knowledge of GMP and experience in sterile manufacturing are essential. Join the team and contribute to innovative practices that improve patient outcomes worldwide.

Benefits

Competitive salary

Comprehensive benefits package

Opportunities for professional development

Qualifications

• Must be a registered Qualified Person under UK/EU law.
• Strong GMP knowledge required, with sterile manufacturing experience preferred.
• Excellent communication skills and ability to solve problems effectively.

Responsibilities

• Act according to EU and UK regulations for QP and GMP standards.
• Certify product batches for market release.
• Provide guidance on quality systems and regulatory compliance.
• Collaborate with teams to support manufacturing operations.
• Ensure compliance readiness during audits and inspections.

Skills

Current eligibility and registration as a Qualified Person under UK/EU law

Strong knowledge of GMP and pharmaceutical quality systems

Excellent communication and problem-solving skills

Ability to work effectively in a global environment

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