Quality Assurance Specialist

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

Job summary

A leading company offers an exciting opportunity for a Quality Specialist within a Global Development Quality team. This role involves reviewing clinical batch records, ensuring compliance with GMP standards, and contributing to life-saving treatments. Candidates should have a scientific background and possess strong organizational and communication skills.

Qualifications

• Strong attention to detail and organizational skills are required.
• Excellent communication and interpersonal abilities needed.
• Ability to work independently and manage multiple priorities.

Responsibilities

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

Skills

Attention to detail

Organizational skills

Communication

Interpersonal abilities

Education

Bachelor’s degree in a scientific discipline

Job description

Social network you want to login/join with:

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.