Quality Assurance Officer II

Location: Kingston upon Hull

# Quality Assurance Officer II
* 15802
* * Permanent*£41,000 - £53,000

Site Based Oxfordshire, United Kingdom Updated on: 13-09-2026

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** ROLE OVERVIEW
** We are currently looking for a Quality Assurance Officer II to join a leading biotech/pharmaceutical organisation based in a collaborative and innovative environment. This is an exciting opportunity for a skilled QA professional to contribute to the development, implementation, and maintenance of essential quality systems that ensure compliance and product  this role, you will play a pivotal part in supporting batch reviews, managing quality investigations, and driving continuous improvement initiatives.

You will work closely with cross-functional teams, external vendors, and regulatory bodies to uphold the highest standards of GMP compliance and assist in audit preparations and execution.
** KEY DUTIES AND RESPONSIBILITIES
** Your duties as the Quality Assurance Officer II will be varied however the key duties and responsibilities are as follows:
* Provide guidance and coordination in the development, implementation, and maintenance of Quality Assurance systems and activities.
* Manage batch review and final quality review activities supporting QP release and prioritisation.
* Drive improvement of GMP compliance, Change Controls, Deviations, and CAPA systems.
* Lead thorough root cause investigations and quality improvement activities.
* As the QA Officer II, you will review and approve SOPs, validation documents, GMP records, and other quality documentation.
** ROLE REQUIREMENTS
** To be successful in your application to this exciting role as the QA Officer II we are looking to identify the following on your profile and past history:
* Experience of Assays
* Proven extensive experience (5+ years) working within quality within a pharmaceutical environment.
* Experienced working within Aseptic manufacturing environments
** WHAT’S IN IT FOR YOU?
** Joining our client offers the opportunity to work at the forefront of biotech and pharmaceutical manufacturing, supporting critical quality functions, and developing your expertise in a dynamic industry setting. You will be part of a collaborative team committed to excellence and continuous improvement, with access to ongoing training and development.

Key Words:
* Quality Assurance* /
* GMP* /
* Regulatory Compliance* /
* Batch Review* /
* Root Cause Investigation* /
* CAPA* /
* Audit* /
* Risk Management* /
* Vendor Oversight* /
* Process Improvement
*