Qualified Person

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We are supporting a growing pharmaceutical company with a strong pipeline and established manufacturing operations, as they look to appoint a Qualified Person (QP) to join their Quality and Supply organisation. This is a permanent role offering long-term impact, high visibility, and an opportunity to contribute to both commercial and clinical product release in a specialist setting.

Key Responsibilities:

• Act as a named QP for the certification and release of licensed and investigational medicinal products
• Ensure all batches meet regulatory, GMP, and internal quality requirements prior to release
• Work closely with Quality Assurance, Manufacturing, Regulatory Affairs, and Supply Chain functions
• Participate in internal and external audits, including those by regulatory authorities
• Support continuous improvement of quality systems and manufacturing processes
• Provide expert guidance on GMP compliance and regulatory expectations across the site

Candidate Requirements:

• Eligible to act as a QP in the UK
• Significant GMP experience within pharmaceutical manufacturing, ideally across both clinical and commercial environments
• Excellent knowledge of quality systems, regulatory frameworks, and pharmaceutical supply chain requirements
• Strong communication skills and a collaborative working style
• Ability to operate effectively in a high-standard, fast-paced environment

What the Role Offers:

• The opportunity to play a key leadership role within a specialist pharmaceutical organisation
• Visibility across manufacturing, quality, and regulatory functions
• A supportive, flexible working environment with a strong focus on quality and compliance

• Seniority level
  
  Mid-Senior level

• Employment type
  
  Full-time

• Job function
  
  Science, Quality Assurance, and Supply Chain
• Industries Pharmaceutical Manufacturing, Biotechnology Research, and Research Services

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