Radiopharmacy QC Radiochemist — GMP QA & Analysis

Alliance Medical Ireland; Dublin; On-site; EUR 52,000 - 70,000; Full time

Job summary

Alliance Medical Ireland is expanding its Radiopharmacy Unit in West Dublin and seeks a Quality Control Radiochemist to ensure the QC of radiopharmaceuticals under EU GMP guidelines. You will contribute to start-up, operation and ongoing development of a state-of-the-art facility, performing analyses, maintaining equipment and drafting compliant QC documents.

The role is full-time (37.5 hours/week) with duties spanning early-morning production coordination, QC analyses, documentation and method

Qualifications

• A recognised qualification/degree in natural sciences or human/veterinary medicine.
• 2 years of relevant industry lab work experience.
• Experience in radiochemistry and GMP.
• Ability to produce clear reports.
• Ability to work in a team environment.
• Method optimisation experience.

Responsibilities

• Coordinate within a team for early morning production and distribution times, starting around 3 am.
• Perform GMP-compliant QC analyses of radiopharmaceuticals.
• Document QC results accurately and ensure compliance with EU GMP guidelines.
• Inspect and maintain analytical equipment.
• Validate/qualify procedures and support new analytical method development.
• Assist in development and establishment of GMP-relevant QC documents.
• General lab tasks including preparing buffers and solvents.
• Other duties as required by management.

Skills

Radiochemistry

GMP

Producing reports

Teamwork

Method optimisation

Education

Degree in natural sciences or veterinary/animal medicine

Tools

pH meter

TLC

HPLC

GC

Activimeter/Dose calibrator

Gamma-ray spectrometer

BET/LAL

Job description

Alliance Medical Ireland is expanding its Radiopharmacy Unit in West Dublin and seeks a Quality Control Radiochemist to ensure the QC of radiopharmaceuticals under EU GMP guidelines. You will contribute to start-up, operation and ongoing development of a state-of-the-art facility, performing analyses, maintaining equipment and drafting compliant QC documents.

The role is full-time (37.5 hours/week) with duties spanning early-morning production coordination, QC analyses, documentation and method