Reporting to the QC Manager, the selected candidates will be responsible to: Carry out analysis on finished sterile and non-sterile products, according to approved monographs or methods using various analytical equipment within an EUcGMP environment.
The role is intended for candidates looking to broaden their knowledge base to various analytical techniques commensurate with the analysis of various dosage forms and garner expertise in physical parameters testing, chromatography (HPLC/UPLC/GC), Dissolution, and handling of sterile products in general. The ideal candidates would be: In possession of a degree in Pharmacy, Chemistry, or a related science subject. Candidates having the BTEC National Diploma in Applied Science will also be considered. Have excellent organisation and communication skills. Be able to work on own initiative, as well as in a team and under pressure to meet pre-set deadlines.
