Qualified Person

Matrix Recruitment Group; Tipperary; On-site; EUR 90,000 - 120,000; Full time

Job summary

Matrix Recruitment Group is seeking an experienced Qualified Person to certify and release medicinal products in line with EU GMP requirements. You will collaborate with QA, Manufacturing, Supply Chain and Regulatory Affairs to ensure compliance and product quality.

The role offers visibility across the business, opportunities to influence quality culture, and involvement in continuous improvement initiatives within a GMP manufacturing environment.

Qualifications

• Eligible to act as a Qualified Person under EU legislation.
• Experience working in a GMP-regulated pharmaceutical manufacturing environment.
• Strong knowledge of EU GMP guidelines and regulatory requirements.

Responsibilities

• Certify and release medicinal product batches in line with EU GMP and regulatory requirements.
• Ensure products are manufactured, tested, and released in compliance with marketing authorisations and GMP.
• Review batch documentation, deviations, investigations, and change controls prior to release.
• Provide expert GMP and quality guidance to cross-functional teams.
• Support internal and external audits and regulatory inspections.
• Contribute to quality risk management, CAPA implementation and continuous improvement.

Skills

EU GMP knowledge

QA collaboration

Attention to detail

Regulatory knowledge

Cross-functional communication

Education

Pharmacy degree

Job description

What You Need to Know

An exciting opportunity has arisen with a leading pharmaceutical company seeking an experienced Qualified Person (QP) to join their growing team. This is an excellent opportunity for a quality-focused professional looking to play a key role in ensuring compliance, product quality, and patient safety within a dynamic GMP manufacturing environment.

Your New Job

As the Qualified Person, you will be responsible for the certification and release of medicinal products in line with EU GMP requirements. Working closely with Quality Assurance, Manufacturing, Supply Chain, and Regulatory Affairs teams, you will ensure products meet all regulatory and quality standards before release. This is a highly visible role offering the opportunity to influence quality culture and support continuous improvement initiatives across the business.

Key Duties and Responsibilities

• Certify and release batches of medicinal products in accordance with EU GMP and relevant regulatory requirements
• Ensure all products are manufactured, tested, and released in compliance with marketing authorisations and GMP guidelines
• Review batch documentation, deviations, investigations, and change controls prior to product release
• Provide expert GMP and quality guidance to cross-functional teams
• Support internal and external audits, including inspections by regulatory authorities
• Contribute to quality risk management, CAPA implementation, and continuous improvement initiatives
• Work closely with manufacturing and quality teams to resolve quality-related issues efficiently
• Maintain up-to-date knowledge of evolving pharmaceutical regulations and industry best practices

What Are We Looking For

• Eligible to act as a Qualified Person under EU legislation
• Degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related scientific discipline
• Previous experience working within a GMP-regulated pharmaceutical manufacturing environment
• Strong knowledge of EU GMP guidelines, quality systems, and regulatory requirements
• Excellent attention to detail with strong decision-making and problem-solving skills
• Ability to communicate effectively and build strong working relationships across multiple departments
• A proactive approach with the ability to manage priorities in a fast-paced environment

Company Culture

We Value Your Trust.