Senior QA Officer

ROLE OVERVIEW

We are currently looking for a Senior QA Officer to join a leading nuclear medicine company based in our client’s Oxford Radiopharmacy facility. This is an exciting opportunity for a dedicated professional to become a vital part of a global leader in radiopharmaceutical development, manufacturing, and distribution. The role offers the chance to work in a dynamic environment dedicated to innovative healthcare solutions, supporting the delivery of life-changing treatments to patients worldwide.

This full-time, onsite position involves ensuring site compliance with GMP standards, international pharmaceutical legislation, and company quality requirements. It’s perfect for someone with substantial quality assurance experience and a proven track record in GMP environments, looking to contribute to a company committed to excellence and innovation in nuclear medicine.

KEY DUTIES AND RESPONSIBILITIES

Your duties as the Senior QA Officer will be varied, but the key duties and responsibilities include:

• Ensuring site compliance with GMP, international pharmaceutical legislation, and company standards.
• Reviewing and approving validation reports, SOPs, and quality documentation to maintain audit readiness and ongoing compliance.
• Supporting investigations related to deviations, incidents, OOS results, and CAPA processes to uphold quality standards.
• Assisting in preparing for regulatory inspections, ensuring ongoing inspection readiness and timely completion of corrective actions.
• Managing all elements of the Quality Management System, including deviations, complaints, change controls, and trending activities.

ROLE REQUIREMENTS

To be successful in your application for the Senior QA Officer role, we are looking to identify the following on your profile and work history:

• A Degree or higher qualification in Pharmacy, Chemistry, Pharmaceutical Chemistry, or Biology.
• Proven experience in quality systems within GMP-compliant facilities, with extensive knowledge of current EU GMP guidelines.
• Significant experience managing quality documentation, investigations, and audit processes in a regulated environment.

WHAT’S IN IT FOR YOU?

Joining our client offers the opportunity to work within a pioneering company dedicated to innovation in nuclear medicine. You’ll be part of a collaborative team with access to professional development opportunities, a competitive salary, and benefits including a performance-based bonus. Additionally, you’ll contribute to a company that values quality, integrity, and the well-being of its patients and employees alike.

Key Words: Senior QA / Quality Assurance / GMP / Regulatory Compliance / Validation / Investigations / Audit Readiness / Microbiology / Radiopharmaceuticals / Inspection Readiness / Continuous Improvement / Team Collaboration / On-site / Oxford Radiopharmacy

"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.