Quality Assurance Specialist

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

Job summary

A leading global company is seeking a motivated Quality Specialist to join their Global Development Quality team. The position involves reviewing clinical batch records to ensure regulatory compliance and maintaining high standards of data accuracy. Candidates should possess a science degree and strong attention to detail, with preferred experience in QA or GMP environments.

Qualifications

• Degree in Chemistry, Biology, or Pharmacy required.
• Strong attention to detail and excellent communication skills.

Responsibilities

• Perform final review of clinical batch records for GMP compliance.
• Compile and approve data packs for QP release.
• Collaborate with global teams to manage documentation.

Skills

Attention to detail

Organizational skills

Communication

Interpersonal abilities

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.