Background

Wiltshire, United Kingdom
I am an analytical chemist with thirteen years' experience in the pharmaceutical industry. I have worked for a number of reputable companies in the sector. During this time I have gained a broad range of experience, from QC analysis, Stability analysis, validation and research and development. I am currently employed as an analytical 'bench' chemist, but have experience and a proven track record at a higher level. I would like to return to that level, either in a more senior technical capacity or in a project/team leadership role. My career history is listed below, if you need to know more get in touch, or leave a post ...

Saturday 10 October 2009

The Beginning ...

I am currently searching for my next employment opportunity. This is the first time I have published a blog, but it seemed a potentially useful addition to the usual recruitment channels. Hopefully, if I get it right, it should increase my visibility to potential recruiters. Let me know what you think, especially if you think I can improve on what I have done so far -or if you have the opportunity that might just be what I am looking for ...

My Career So Far ...

Scientist

September 2007 – Present

  • Performed analytical development experiments on new drug compounds
  • Developed and validated analytical methods.
  • Performed stability analysis and prepared stability reports.
  • Performed in-process analysis, in support of scale-up manufacturing and technology transfer projects –including preparation and issue of reports.

Project Leader

July 2006 – September 2007

  • Reviewed current analytical chemistry methodology, advised on potential areas for improvement/optimization.
  • Developed and validated new analytical methods where necessary.
  • Validated new analytical equipment for the QC Chemistry laboratory.
  • Trained QC Chemistry analysts in use of new equipment and methods.
  • Prepared SOPs, protocols –including technology transfer protocols, equipment IQ, OQ, PQ and associated reports.
  • Coordinated and contributed to cross functional validation activities.
  • Participated in analytical investigation/root cause analysis committees.

Higher Analytical Scientist

October 2005 – July 2006

  • Performed analytical development experiments on new drug compounds.
  • Transferred, developed and validated analytical methods and equipment.
  • Prepared SOPs, protocols and reports, for use in-house and externally.

Analytical Development Scientist

April 2005 – September 2005

  • Performed solubility enhancement experiments on new drug compounds.
  • Transferred, developed and validated analytical and cleaning verification methods.
  • Prepared SOPs, protocols and reports, for use in-house and externally.

Pharmaceutical Scientist

October 2003 – March 2005

  • Analysed propriety formulations for drug content by HPLC and surface area by nitrogen adsorption.
  • Assisted in the development of MaxSol technology platform, including optimisation of methods for drug content analysis by HPLC.

Senior Research Associate

January 2003 – September 2003

  • Contributed to preformulation studies on new chemical entities.
  • Determined the solid-state physical properties of NCEs by various techniques, inc. XRPD, DSC, TGA and GVS.
  • Implemented HPLC assay platform to determine purity of NCEs.
  • Developed and implemented assay platform for determining thermodynamic/kinetic solubility of NCEs.
  • Screened salt-forms of drug candidates for purity, solubility and intrinsic dissolution rate.

QC Shift Analyst

September 2001 – January 2003

  • Analysed finished solid dose and controlled release pharmaceutical products and raw materials in a GLP environment.
  • Shift Lead for maintaining and calibrating laboratory equipment.
  • Reviewed results produced by other analysts and performed investigations.

QC Analyst

April 1997 – August 2001

  • Analysed finished solid dose pharmaceutical products, to in-house and client methods –in a GMP environment. Trained, mentored and supervised less experienced analysts.
  • Validated analytical methods.
  • Maintained and calibrated laboratory equipment.
  • Prepared SOPs for use in the laboratory.

Followers