Quality Assurance Officer II

# Quality Assurance Officer II*15802**Permanent*£41,000 - £53,000Site BasedOxfordshire, United Kingdom Updated on: Apply 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* #J-18808-Ljbffr