Quality Assurance Officer II

Hyper Recruitment Solutions Ltd; United Kingdom; Remote; GBP 41,000 - 53,000; Full time

Job summary

Hyper Recruitment Solutions Ltd is assisting a leading biotech/pharmaceutical organisation based in Oxfordshire to hire a Quality Assurance Officer II. The role focuses on developing, implementing, and maintaining quality systems to ensure GMP compliance and product integrity.

You will support batch reviews, drive CAPA and change controls, and lead root-cause investigations while collaborating with cross-functional teams and regulators to uphold high standards.

Qualifications

• Experience of Assays
• Proven extensive experience (5+ years) working within quality within a pharmaceutical environment.
• Experienced working within Aseptic manufacturing environments

Responsibilities

• 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

Skills

Quality Assurance

GMP

Regulatory Compliance

Batch Review

Root Cause Investigation

CAPA

Audit

Risk Management

Vendor Oversight

Process Improvement

Job description

# Quality Assurance Officer II*15802**Permanent*£41,000 - £53,000Site BasedOxfordshire, United Kingdom Updated on: 13-09-2026Apply Now**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 integrity.In 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*