Company Description: Vieco Pharmaceuticals, founded in 2014, is a pharmaceutical factory in JAFZA, Dubai, producing solid (Tablets and Capsules), Liquid (Syrups), and semi-solid (Ointments and Creams) pharmaceutical products. established to meet the rising demand for high-quality medicines in the region. The company focuses on using the latest pharmaceutical production technologies while adhering to international standards.
Responsibilities:
o Perform pre-formulation studies including physicochemical characterization, solubility, stability screening, and compatibility assessment of APIs and excipients.
o Perform formulation development studies for oral solid, semisolid, and liquid dosage forms, including trial batches and optimization runs.
o Perform analytical method validation studies, protocols, and final reports.
o Perform recovery studies and execute cleaning validation and verification runs.
o Analyse raw materials as required.
o Perform physicochemical testing of samples during product development per approved SOPs.
o Perform analytical transfer analysis per respective protocols.
o Prepare and execute development stability protocols and final reports.
o Perform chemical and physical testing at development stability time points.
o Calibrate instruments per work instructions to ensure compliance with standards.
o Issue and sign specifications and test certificates.
o Prepare and document pre-formulation, formulation, and analytical characterization in the respective product development report.
o Report and participate in OOS and NCR investigations via AmpleLogic eQMS.
o Handle deviations, lab incident reports, and CAPAs via AmpleLogic eQMS.
o Prepare SOPs on AmpleLogic eDMS.
o Perform any other tasks as assigned
Qualifications:
Bachelor of Pharmacy / Master of Pharmacy
More than 5 years of experience in the pharma field
Relevant Experience in R & D
