About The Role

What can we offer you?

Apart from job satisfaction, we can offer you

YOURSELF

25 days’ holiday (with the option to buy more)

HEALTH

Private Healthcare
Optional dental insurance, health assessments and health cash plans
Cycle to Work scheme

WEALTH

Company Pension Scheme, matching contributions up to 5% of salary
Life assurance
Annual staff bonus scheme
Season ticket loans

Job Summary

In this role you'll perform QC method development and routine analysis of PET radiotracers to support clinical and pre-clinical studies in a GMP environment.

Job Responsibilities

QC of assigned radiotracers according to project distribution and the scanning schedule.
QC implementation of newly assigned radiotracers: method development, validation and documentation.
Providing routine QC support to clinical and pre-clinical studies.
Providing analytical chemistry support for precursor characterization, radiotracer and radioligand purification.
Data processing including HPLC and GC.
Documenting QC records to ensure compliance with cGMP.
Raising and investigating Out Of Specification (OOS) results and Deviation within QMS.
Presenting technical QC issues to internal and external audits, if required.
Training and educating others in your area of expertise.
Keeping up to date with relevant procedures and policies, as well as new analytical techniques and processes (small molecules and biological products).
Presenting results to internal and external audiences, when required.
Maintaining adequate stocks of laboratory supplies
Completing routine laboratory tasks, e.g., preparing HPLC buffers, calibration standards, etc.

Required Skills

Minimum 2 years' experience in a QC laboratory.
Experience in HPLC
Experience in a GMP environment

Knowledge and Preferred Skills

Experience in GC is an advantage.
Experience working with short-lived radioisotopes preferable (especially carbon-11 and fluorine-18) is desirable.
Experience in change control is preferable.