QC Radiochemist - Radiopharmaceuticals, GMP Training

We have a fantastic opportunity for a QC Radiochemist to join our Radiopharmacy Team.

If you are a newly qualified graduate or an experienced individual with an Analytical Chemistry background looking for a challenging yet rewarding career, then this may be the opportunity you are looking for.

Candidates working in QC will report to the QC Manager and shall receive training in all aspects of radiopharmaceutical testing for release including GC, HPLC, r-TLC, Gamma spectroscopy etc. Extensive training in Good Manufacturing Practice (GMP), radiation safety and Quality Management Systems will be delivered to all.

Radiopharmaceuticals by their very nature have an extremely short shelf-life. As such these roles will entail unsocial hours and shift work. This is reflected in the remuneration with a local shift pattern to assure a harmonious work-life balance is maintained.

The role includes routine progress assessments and staged salary uplifts that are awarded as training milestones are achieved.

Hours of work for the roles are 40 hours per week Monday-Sunday.

We are inviting applications from newly and experienced graduates from a scientific background. To be considered for the role you must hold a BSc/MSc (or expect to graduate at the end of this academic year).

Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date.

Operate and maintain routine protocols for the chemistry laboratory in strict adherence to GMP and relevant EU pharmacopoeia standards. Manage raw material sampling, testing and release system.

Ensure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including HPLC (radio chemical and chemical purity of 18F FDG), Gas Chromatography, pH measurement, Osmolality and LAL.

Maintain records of faults on any dysfunction - operational or equipment.

In association with the QC Manager to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard PET tracers.

Ordering of chemicals, glassware, cleaning and other consumables for routine QC analysis. Formulation of reagents for radiochemistry, mixing of solvents for HPLC and other analyses, cleaning of glassware and disposal of waste chemicals and materials.

Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by QAand adoption by the unit.

Provide training and support for others selected as rota / backup in undertaking routine QC operations.

Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules.