Description
QUALIFICATIONS: Pharm. D (Doctor of pharmacy) University College of pharmacy, University of the Punjab. PRACTICAL SKILLS GAINED DURING MY DEGREE: * I.R spectra and analysis, HPLC. Thin Layer Chromatography. UV and KF Titrator. * Wide knowledge of pharmaceutical development and analytical testing requirements. * Good understanding of pharmaceutical compositions and processing perspective. Familiarity with pharmaceutical production, G.M.P, elementary processes, fabrication processes, profound knowledge of industrial pharmacy. * Ability to prepare and dispense drugs and pharmaceutical preparations. * Packaging material analysis and maintenance of record. * Testing of raw materials such as solubility, titration, dissolution, and assay where required, and assay of grains. Furthermore, assay of finished sample is also performed according to B.P and U.S.P. Stability testing of accelerated pharmaceutical products after 6 months. It was a 8 months work experience in Schazoo pharmaceutical laboratories (SPL) in Research and Development Department. What I learnt in laboratory is as under. "Receiving of sample materials and unit carton design type and product name from planning department. We conduct trials on the sample materials given and type of dosage forms that we prepare. We prepare dossiers and SOPS in collaboration with the quality assurance department. We design the instrumentation for testing the raw materials. We design the types of machines and their instruments for the production department. For testing of materials in large quality control department assists us in many ways. I make 3 genuine reports of one product against one protocol and BMR. After consulting with manager these reports are sent to the director of the plant and then a copy of which is retained back. Much work for testing I conducted was on hplc both for batch and for the dissolution in case of stability testing." In case of packing materials say unit carton width length height grammage proof reading clarity of appearance compliance of colour with standard are recorded manualy in packing materials register. If it falls under the given limit as per SOP of packing materials the sample is accepted otherwise rejected.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| (Confidential) | Principal | / - Present |
Accomplishments
Highlights:
Keywords
