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The role is covered in the following locations: Edinburgh

Company Information

My client are a specialty vaccine company across several infectious diseases. They are soon to launching a new vaccination in the UK and the company has more than 700 employees across 6 countries.

Role Overview

Duties will include:

To represent the company to external authorities on liaison with MHRA with regards to product defect reporting
Manage the batch disposition process and file compilation
Oversee the systems and processes for the management of product technical complaints
Assist with the preparation, review and approval of quality agreements
Internal & external audits
Implement and maintain Standard Operating Procedures

Key Duties and Responsibilities

Excellent base salary
Company bonus
Stock options (LTI)
25 days holiday

Person Specification

Eligible QP (UK qualified, under the Permanent Provisions)
Relevant experience of UK, EU and FDA cGMP requirements.
Good understanding and working knowledge of the Pharmaceutical Industry


The Qualified Person will be overseeing the review, approval and certification of products, maintaining internal and external manufacturing testing activities whilst adhering to UK, EU and FDA regulatory requirements. This permanent position is based at my clients location in Scotland.

05 Dec 2023

Alex Martin

Recruitment Team Leader 01494 818 028

Marcus Chalk

Specialist Recruiter 01494818003

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¿Por qué Zenopa?


legal    public protection    public health    product safety