Responsabilities:
– Conduct stability studies of intermediates and active subtances as per predefined protocol , data compilation and evaluation as per ICH guidelines.
– Analysis of finished products as per the specifications, MoA and data compilation.
– Analytical method validation protocol , execution and final report preparation.
– Analytical method transfer
– Write standard operation procedures, analyticcal tests methods, protocols/reports for various analytical projects , or stability reports, when required.
– Review of data generated by chemist
– OOS and investigation reports
– To ensure that all the work is carried out in compliance with the required standards, conforming to company, cGMP, SOPs, regulatory regulations and guidelines, safety and evironmental guidelines.
Experience:
Candidates will need to show evidence of the following :
- Preferably hold a degree in Chemistry
- Very high english level is a must.
- Must have a minimum of three years of previous experience of working within a QC Lab , but experience in analytical development will be also valuable.
- Theoretical and practical knowledge of various analytical techniques such as HPLC, GC, GC-HS, IC, FT-IR, PSD, KF titration
- Extremely organised to deal with a variety of projects and able to priorities conflicting demands.
- Abitly to work under pressure with multiple projects to strict on-going deadlines.
- Excellent communication skills (oral and written) and interpesonal skills.
