QA Specialist

CK Group- Science, Clinical and Technical; Chester; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading global pharmaceutical company is seeking a QA Specialist to join their team on a contract basis for 9 months. This role involves reviewing batch documentation, supporting investigation of quality incidents, and ensuring adherence to regulatory standards. The position allows for a hybrid working model based in Chester. The ideal candidate will have a degree in a science-based subject with extensive pharmaceutical industry experience.

Qualifications

• Extensive experience in the pharmaceutical industry.
• Labelling experience in the pharmaceutical industry is desirable.
• Understanding of pharmaceutical or medical terminology.

Responsibilities

• Review batch and test documentation for investigational medicinal products.
• Support investigation of non-conformances and quality incidents.
• Review and approve vendor-generated label proofs/specifications.

Skills

Pharmaceutical documentation practices

Regulatory principles understanding

Proficiency in Microsoft Suite

Education

Degree level qualification in a science-based subject

Job description

Overview

CK Group is recruiting for a QA Specialist (GMP) to join a global pharmaceutical company on a contract basis for 9 months.

Salary

Paying up to £20 per hour PAYE

QA Specialist Role

• Review all batch and test documentation associated with investigational medicinal products (IMPs) and packaging components.
• Support in the investigation of non-conformances and quality incidents.
• Resolve and documents any deviation or problem relating to the audit of documents.
• Track and trend deviation investigations and CAPA.
• Review client and label vendor specifications in accordance with relevant regulatory requirements.
• Review and approve vendor-generated label proofs/specifications and other related documents.

Your Background

• Educated to Degree level qualification, ideally in a science-based subject
• Relevant and extensive experience in the pharmaceutical industry.
• Labelling experience in the pharmaceutical industry is highly desirable.
• Ability to understand and apply regulatory and CGMP principles.
• Good understanding of pharmaceutical or medical terminology
• Proficiency in standard office technology, including Microsoft Suite (Outlook, PowerPoint, Excel)
• Good knowledge of rigorous pharmaceutical and/or scientific documentation practices and change control processes (e.g., revision control) is preferred.

Company

Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.

Location

This role is based at our clients site in Chester, but allows for 50/50 hybrid working (50% from home, 50% from office)

Apply

For more information, or to apply for this QA Specialist please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (phone number removed).

It is essential that applicants hold entitlement to work in the UK

Please note:This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check