Quality Assurance Specialist

JR United Kingdom; Luton; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading company in global development is seeking a motivated Quality Assurance Specialist based in Luton. The role involves reviewing clinical batch records ensuring compliance with GMP, collaborating with supply chain teams, and maintaining high standards for life-saving treatments. Candidates should possess a scientific degree and have strong organizational and communication skills, with preference for prior experience in QA environments.

Qualifications

• Bachelor’s degree in a scientific discipline.
• Strong attention to detail and organizational skills required.
• Experience in QA or GMP environments preferred.

Responsibilities

• Perform final review of clinical batch records for compliance.
• Compile and approve data packs for Qualified Person (QP) release.
• Collaborate with global supply chain teams and manage documentation.

Skills

Attention to detail

Organizational skills

Communication

Interpersonal abilities

Independence

Education

Bachelor’s degree in Chemistry, Biology, or Pharmacy

Job description

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Quality Assurance Specialist, luton, bedfordshire

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Client:

Planet Pharma

Location:

luton, bedfordshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

1

Posted:

04.06.2025

Expiry Date:

19.07.2025

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Job Description:

An exciting opportunity is available for a motivated and detail-oriented Quality Specialist to join a Global Development Quality team. This role offers exposure to a wide range of investigational medicinal products, from small molecules to advanced immunotherapies, contributing directly to the delivery of life-saving treatments to patients.

Key Responsibilities:

• Perform final review of clinical batch records to ensure compliance with GMP and regulatory filings.
• Compile and approve data packs for Qualified Person (QP) release.
• Collaborate with global clinical supply chain teams and manufacturing sites (internal and external).
• Manage issue resolution and ensure timely documentation and communication.
• Maintain high standards of accuracy and compliance throughout the review process.

Qualifications & Skills:

Required:

• Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy).
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities.
• Ability to work independently and manage multiple priorities.

Preferred:

• Prior experience in a QA or GMP-regulated environment.
• Familiarity with clinical manufacturing and regulatory compliance processes.