- Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods.
- Creating and following up maintenance plan for all instruments in R&D analysis lab.
- Securing & following up availability of all analytical resources (Columns, reference standards, reagents, solvents …..etc).
- Sampling and testing of raw materials, intermediates and finished products using current pharmacopoeias, any associated ‘wet’ chemistry and instrumental techniques (HPLC, IR, UV), as appropriate.
- Preparing R&D reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (CoA) (for finished products) and stability reports.
- Stability testing of products for new formulations and ongoing stability trials, using physical (pH, viscosity) and instrumental (HPLC, UV) techniques, as appropriate.
- Writing/reviewing Standard Operating Procedures (SOPs).
- Supervise, develop and train R&D analysts.
- Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion.
- Observing and complying with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP).
- Observing and complying with company Health and Safety Policies.
- Observing and complying with company Standard Operating Procedures (SOPs)
- Review SOPs related to R&D department.
- Review CTD, export & MOH registration files.
Experience:6-9 years.Education:Bachelor in Pharmacy & Pharmaceutical Sciences.Technical Training:Analytical method validation.Development of analytical methods.Knowledge:Highly proficient in the use of key analytical equipment (HPLC, GC, IR, UV) and the testing of finished products.Good IT skills e.g. Microsoft Office (Word, Excel, PowerPoint and Outlook).Abilities:Ability to operate analytical instruments, analyzing information.Ability to report and document analytical results.Ability to read and write English language fluently.