Qualified Person

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Removing Recruitment Stress in Life Sciences - Director at Nexia

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

Seniority level
Mid-Senior level

Employment type

Employment type
Full-time

Job function

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

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