Within this Analytical Development Scientist role you will provide analytical support to the development and manufacture of a wide range of dosage forms from early formulation studies and clinical trial manufacture to NDA registration. The work is very varied and includes method development and validation, provision of support during formulation development and manufacture, release testing and stability studies.
Our client is a global CMO based in Wiltshire. The nature of the environment is fast paced. As such you would have a number of projects to work on at any one time spanning a diverse product, dosage form and client range. With this in mind good organisational skills are essential.
To be considered for this Analytical Development Scientist role, it is essential that you have considerable experience in reversed phase HPLC / UV / DAD detection, sample preparation (solid phase, liquid and solvent extraction) and method development / validation.
You must be qualified in Chemistry or a related subject (or equivalent) and previous laboratory experience, preferably in pharmaceutical analytical development is required. Proven experience in HPLC method development and validation are essential. You will also have experience of working to cGLP / GMP and will have used the techniques as described above as well as GC, UV and dissolution techniques.
For more information or to apply for this Analytical Development Scientist position, please contact Jason Johal at CK Science on 01438 723 500 or email email@example.com. Please quote reference ST20890 in all correspondence.