Senior Qualified Person: GMP & Batch Release Expert

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

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.