EDUCATION / EXPERIENCE REQUIRED:

• B.S./M.S. degree in Analytical Science, Chemistry, Pharmacy, or equivalent industry experience, with minimum 1-3 years’ experience in a laboratory-based role, primarily in pharmaceutical industry.
• Experience of working to industry expectations for data integrity within a non GxP environment.
• Knowledge and experience of bio-enhancement techniques to improve drug solubility
• Knowledge and experience of in vitro characterisation methods such as solubility and dissolution
• Some knowledge and experience of solid state analytical methodologies such as X-Ray powder diffraction and Raman spectroscopy.

SUMMARIZED PURPOSE:

In this role you will perform Bio-enhancement and pre-formulation characterization studies to support oral formulation development. This will include performing in vitro performance analysis to assess improvements to solubility/bioassessability using a range of techniques and to exploring sample preparation to improve bio-enhancement outcomes.
This position is based at our client site in Stevenage, travel to the Ware site may also be required.

RESPONSIBILITIES:

• Perform screening assessment of various bio-enhanced formulation options using a variety of techniques including spray drying (SD), small scale hot melt extrusion (HME), lipid based formulations (LBFs) and size reduction via micronisation and cryo-milling.
• Perform physical characterisation using techniques such as differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), microscopy (Optical and Hot Stage), xray powder diffraction (XRPD), scanning electron microscopy (SEM), Raman spectroscopy, particle size analysis , rhelogy and viscometry.
• Perform in vitro performance analysis using HPLC, Mass Spectrometry, UV-Spectroscopy, dissolution, artificial membrane permeability
• Complete the write-up of experimental results on electronic notebook system, provide technical reports for all work conducted and present findings/recommendations to project leads/supervisors
• Participate in Lab meetings - raising safety and quality concerns and participate in management/housekeeping audit activities