Quality Assurance Specialist

JR United Kingdom; Peterborough; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading company in global development is seeking a motivated Quality Assurance Specialist in Peterborough. The role involves ensuring the quality of investigational medicinal products through compliance reviews, issue resolution, and collaboration with clinical supply chain teams. Ideal candidates will possess a scientific degree and strong attention to detail.

Qualifications

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

Responsibilities

• Perform final review of clinical batch records for compliance with GMP and regulatory filings.
• Compile and approve data packs for Qualified Person release.
• Collaborate with global clinical supply chain teams and manage issue resolution.

Skills

Attention to Detail

Organizational Skills

Communication

Interpersonal Abilities

Education

Bachelor’s degree in scientific discipline

Job description

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Quality Assurance Specialist, peterborough

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Client:

Planet Pharma

Location:

peterborough, 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.