Quality Assurance Specialist

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

Job summary

A leading company is offering an exciting Quality Assurance Specialist position in Basingstoke. This role is essential in ensuring the compliance of clinical products with GMP standards, collaborating with global teams, and contributing to life-saving treatments. Candidates should possess a scientific degree and demonstrate exceptional organizational skills to thrive in a fast-paced, detail-oriented environment.

Qualifications

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

Responsibilities

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

Skills

Attention to detail

Organizational skills

Communication

Interpersonal abilities

Ability to work independently

Time management

Education

Bachelor’s degree in a scientific discipline

Job description

Quality Assurance Specialist, Basingstoke

Client:

Planet Pharma

Location:

Basingstoke, UK

Job Category:

Other

Work Arrangement:

Virtual job fairs

EU work permit required:

Yes

Posted:

04.06.2025

Expiry Date:

19.07.2025

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.

Additional Notes:

Please note that if you are NOT a passport holder of the country for the vacancy, you might need a work permit. Check our Blog for more information.

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Created on 04/06/2025 by JR, United Kingdom