ROLE OVERVIEW
We are currently looking for a QA/QC Officer to join a leading provider in the nuclear medicine sector based in our client’s state‑of‑the‑art facility. This exciting opportunity is ideal for professionals with a background in radiopharmacy or laboratory quality control, eager to contribute to innovative healthcare solutions that make a real difference worldwide.
As QA/QC Officer, you will be instrumental in ensuring site compliance with GMP standards, international pharmaceutical legislation, and company requirements. This is a key role supporting the quality assurance and quality control functions within a dynamic, fast‑paced environment, with a focus on maintaining high standards of safety, accuracy, and regulatory adherence.
KEY DUTIES AND RESPONSIBILITIES
- Ensure site compliance with GMP, Specials guidelines, and relevant pharmaceutical legislation through review and oversight of production and analytical methods.
- Manage documentation processes including reviewing, updating SOPs, and writing new procedures to uphold quality standards.
- Support investigation activities related to deviations, OOS results, CAPA, change controls, and release of incoming materials.
- Review QC tests and microbiological results, managing out‑of‑specification outcomes, and ensuring timely record updates.
- Perform analytical method validation, execute validation protocols, and support equipment calibration and requalification activities.
ROLE REQUIREMENTS
- A Degree or higher level in a related science field (e.g., Pharmaceutical Chemistry, Quality Assurance, Quality Management).
- Proven 2‑3 years of radiopharmacy or laboratory experience, with knowledge of GMP compliance and QC processes.
- Familiarity with equipment qualification, process validation, and working within a quality department is highly desirable.
WHAT’S IN IT FOR YOU?
Joining our client offers an excellent platform to develop your career within the innovative field of nuclear medicine. You will be part of a globally recognized organization committed to excellence and continuous improvement. The role provides exposure to cutting‑edge radiopharmaceutical processes, working with a dedicated team in a collaborative environment, alongside competitive salary and bonus potential.
Key Words: QA / Quality Assurance / QC / Radiopharmacy / GMP / Validation / Documentation / Microbiology / Regulatory / Good Manufacturing Practice / Drugs / Pharma / Radiation / Laboratory / Compliance / SOPs / Process Validation / Micro Results / Root Cause Analysis / CAPA / Equipment Calibration / Validation Protocols / Microbiological Testing
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.
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