Thomas Blandford Email & Phone Number

Dartford, England, United Kingdom

Kent Science Park

Worked alongside formulators in assessing feasibility of new product by supporting product development using analytical techniques such as UPLC, GC-HS, Dissolution and Density. Presented data to supplement clinical trial data to internal stakeholders to aide a decision on transferring product from Phase I to Phase II clinical testing. Issued testing CoAs to external CROs. Became an EHS Representative maintaining Safety Standards across all working areas, and became a DEIB Champion promoting… Show more Worked alongside formulators in assessing feasibility of new product by supporting product development using analytical techniques such as UPLC, GC-HS, Dissolution and Density. Presented data to supplement clinical trial data to internal stakeholders to aide a decision on transferring product from Phase I to Phase II clinical testing. Issued testing CoAs to external CROs. Became an EHS Representative maintaining Safety Standards across all working areas, and became a DEIB Champion promoting Neurodiversity across the global workplace. Show less

Queenborough, England, United Kingdom

Senior Analyst also doubling as acting Team Leader for Raw Materials and Commodities including liaising with Contract Laboratories to organise testing for product, sending material and receiving CoAs. Assigned testing plan to analysts and led a team of six people. Attended tiered meetings to support the manufacturing and production plants to ensure product timelines were adhered to. Verified data and released material for use. Lead OOS investigations in-line with current procedures. Created… Show more Senior Analyst also doubling as acting Team Leader for Raw Materials and Commodities including liaising with Contract Laboratories to organise testing for product, sending material and receiving CoAs. Assigned testing plan to analysts and led a team of six people. Attended tiered meetings to support the manufacturing and production plants to ensure product timelines were adhered to. Verified data and released material for use. Lead OOS investigations in-line with current procedures. Created, updated and maintained documentation updates from internal SOPs through to compendial texts. Maintained documentation practices in-line with cGDP requirements including internal audits, and supporting external audits with knowledge when required. Show less

Queenborough, England, United Kingdom

QC Analyst working on cGMP testing on Raw Materials, Commodities, In-Process and Intermediate Product Formulations, Finished Dose drug product and Stability testing using analytical techniques such as HPLC, GC, FT-IR, UV-Vis Spectroscopy, Refractive Index, Brookfield Viscometry, Moisture Determination via KF and LOD, Dissolution, and physical testing including hardness, appearance, dimensions and disintegration.