Qualified Person

Nexia; England; On-site; GBP 50,000 - 70,000; Full time

Benefits offered by this job

Flexible working environment

Visibility across company functions

Job summary

A leading pharmaceutical company in the United Kingdom seeks a Qualified Person (QP) to join their Quality and Supply organization. This permanent role involves acting as a QP for certification of medicinal products and ensuring all batches meet regulatory requirements. The ideal candidate will have significant GMP experience, strong communication skills, and the ability to thrive in a fast-paced environment. Competitive salary and a supportive working environment are offered.

Qualifications

• Significant GMP experience in pharmaceutical manufacturing.
• Ability to operate effectively in a high-standard, fast-paced environment.
• Excellent knowledge of regulatory expectations.

Responsibilities

• Act as a named QP for certification and release of products.
• Ensure batches meet regulatory quality requirements.
• Participate in audits by regulatory authorities.

Skills

Strong communication skills

Collaborative working style

GMP experience

Quality systems knowledge

Regulatory frameworks knowledge

Education

Eligible to act as a QP in the UK

Job description

1 day ago Be among the first 25 applicants

Direct message the job poster from Nexia

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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