Radiopharmaceutical QC/QA Specialist

Curium Live Forward; Newcastle upon Tyne; On-site; GBP 42,000 - 60,000; Full time

Job summary

Curium Live Forward is seeking a Quality Control professional to perform QC on radiopharmaceuticals and assist with maintenance of the Newcastle Radiopharmacy in line with GMP. You will review production methods against EP/BP/SmPC guidelines, update SOPs, and support deviations, CAPA and QMS activities.

Skills include teamwork, attention to detail, good communication, and the ability to manage logs and environmental monitoring. Shift work is required; related science degree preferred.

Qualifications

• Requires a related science degree and quality control experience are desirable.
• Desirable radiopharmacy experience; working knowledge of pharmaceutical chemistry and GMP is required.

Responsibilities

• Quality control on radiopharmaceuticals in compliance with GMP/EP/BP/SmPC
• Review and update SOPs and forms
• Assist with deviations, incidents, investigations and CAPA activities
• Review QC tests and microbiology results and manage Out of Specification results
• Maintain quality records and trackers; ensure GMP compliance across the site
• Support QMS elements including deviations, complaints, CAPA, change control and recalls
• Conduct environmental monitoring and aseptic suite activities including isolators
• Record logs for equipment, fridge/freezer and other QA checks
• Participate in root cause analysis and CAPA identification
• Communicate effectively to enhance production and quality processes

Skills

Team player

Basic computer skills

Customer relations

Communication skills

Practical ability

Timekeeping

Stress management

Attention to detail

Education

Related Science Degree

Quality Control experience desirable

Radiopharmacy experience desirable

Knowledge of GMP

Job description

Curium Live Forward is seeking a Quality Control professional to perform QC on radiopharmaceuticals and assist with maintenance of the Newcastle Radiopharmacy in line with GMP. You will review production methods against EP/BP/SmPC guidelines, update SOPs, and support deviations, CAPA and QMS activities.

Skills include teamwork, attention to detail, good communication, and the ability to manage logs and environmental monitoring. Shift work is required; related science degree preferred.