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Quality Assurance Specialist

JR United Kingdom

City of Edinburgh

On-site

GBP 30,000 - 50,000

Full time

4 days ago
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Job summary

A leading global development quality team is looking for a Quality Specialist. Responsibilities include reviewing clinical batch records and ensuring compliance with GMP standards. Ideal candidates have a scientific background and strong organizational skills. This role provides an opportunity to contribute to the delivery of life-saving treatments.

Qualifications

  • Bachelor’s degree in Chemistry, Biology, Pharmacy or similar required.
  • Strong attention to detail and organizational skills essential.
  • Excellent communication and interpersonal skills needed.

Responsibilities

  • Perform final review of clinical batch records for GMP compliance.
  • Compile and approve data packs for QP release.
  • Collaborate with clinical supply chain and manufacturing teams.

Skills

Attention to detail
Organizational skills
Communication
Interpersonal skills
Independence

Education

Bachelor’s degree in a scientific discipline

Job description

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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.
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