QC Radiochemist

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Date: 12 Mar 2026

Location: Dublin, Ireland, A94 E4X7

Company: curium

About Curium

Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service.

 

With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.

 

Summary of Position


To perform quality control analysis on radiopharmaceuticals for patient use and raw material testing in accordance with principles of Good Manufacturing Practice (GMP).
 

Essential Functions

 

  • Accurately perform Quality Control testing on all manufactured products on site according to MA, GMP and EP guidelines; use of gas chromatography (GC), TLC and HPLC 
  • Manage the Environmental Monitoring process and ensure data is recorded and trended in the QMS
  • Reading Microbiological plates, bioburden and sterility samples
  • Interpretation and recording of Microbiological data and report any out-of-specification, ensuring appropriate action is taken in a timely manner
  • Review and maintain QC logbooks and data to ensure the site meets all its objectives in relation to data integrity policy
  • Perform and manage maintenance and calibration of lab equipment 
  • Partake in validation activities, preparation and execution of protocols 
  • Liaise with Quality Management on validation strategy and training
  • Checking stock level and ordering supplies
  • Endotoxin testing
  • Raw materials testing
  • Goods in check/inspection as part of quality inspections of incoming materials
  • Reviewing compliance of analytical methods with GMP/special guidelines and EP/USP
  • Ensure timely completion and update of all Quality records and trackers
  • Raising and completing deviation reports, OOS, and change controls where applicable
  • Participate in Root Cause Analysis and CAPA identification
  • Effective communication with all colleagues to facilitate efficiency in both production and quality-related matters
  • Maintain paper and electronic records from all QC processes for statutory purposes, including quality control under GMP
  • Comply with the requirements of the Pharmaceutical Good Manufacturing Practice (GMP), Ionising Radiation Local Rules, COSSH and Health & Safety procedure

Requirements

  • Level of professional and intellectual ability
  • Knowledge of Ionising Radiation Local Rules, COSSH and Health & Safety procedure (desirable)
  • Knowledge of working within a GMP environment
  • A willingness to work flexibly and commit to early working hours in a shift pattern.

Education/experience

  • Related Science Degree, i.e. analytical science, chemistry or related discipline
  • Working knowledge of pharmaceutical chemistry and good manufacturing practice is desirable
  • Experience in using QC equipment: GC, TLC, HPLC, and pH meter would be advantageous

Skills

  • Excellent team player
  • Able to work on own initiative
  • Good customer relationship skills
  • Communication skills
  • Practical ability
  • Excellent timekeeping competences
  • Stress handling
  • Excellent attention to detail
  • Full Driving licence (required)
  • Work permit Visa (required)
     

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

 

Equal Opportunity Employer

Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality.  All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.