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.
QC Routines
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.
Maintenance
Ensure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including HPLC (radiochemical and chemical purity of 18F FDG), Gas Chromatography, pH measurement, Osmolality, and LAL.
Faults
Maintain records of faults on any dysfunction - operational or equipment.
Quality Systems
In association with the QC Manager to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard PET tracers.
Materials
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.
Standard Operating Procedures
Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by QA and adoption by the unit.
Training Others
Provide training and support for others selected as rota/backup in undertaking routine QC operations.
Regulatory
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.
#J-18808-Ljbffr