IPQC of Pharmaceutical Dosage Form at Pharmaceutical Industry mahbub tanim
This slides contents some details on In Process Quality Control (IPQC) of pharmaceutical dosage form (tablet, capsule, syrups, sterile etc.) at pharmaceuticals before sent them to Quality Control (QC) department.
IPQC of Pharmaceutical Dosage Form at Pharmaceutical Industry mahbub tanim
This slides contents some details on In Process Quality Control (IPQC) of pharmaceutical dosage form (tablet, capsule, syrups, sterile etc.) at pharmaceuticals before sent them to Quality Control (QC) department.
IPQC cover the entire chain of operations from the receipt of raw material in the warehouse to the release of finished products from the warehouse for distribution and or sale. IPQC is a process where quality of a product is ensured that it meets the standard according to regulatory authority guidline.
IPQC cover the entire chain of operations from the receipt of raw material in the warehouse to the release of finished products from the warehouse for distribution and or sale. IPQC is a process where quality of a product is ensured that it meets the standard according to regulatory authority guidline.
Focused Chemical/Microbiological technician highly effective at following USP methods and GMP practices with pharmaceutical and medical device experience.
Chemist accomplished in GC, HPLC, analytical and assay methods used on raw material and finished products to assure the quality and purity of products. Certified in Clinical Trials and Drug Development and worked side by side a chemical formulator R&D chemist for 3 years. Coordinated process validation procedures, stability program, chemical waste management system, calibration program, laboratory set up, ordering and SOP procedural writing.
Versed Microbiological surface and air quality testing, process validation, microbiological identification, trending, tracking, gram staining techniques and microbiological morphology. Certified in Pharmaceutical Microbiology.
Similar to MOHAMMED AMINUR RAHMAN Final Nov 2014 (1) (20)
1. MOHAMMED AMINUR RAHMAN
4165 75 St. Apt#A6, Elmhurst, NY 11373
Cell: 347-653-0090
Email: aminurrahman80@gmail.com
Objective: Seeking a QC Chemist post in a Pharmaceutical company having a knowledge and experience in this
field. Can be performed in any department in the QC Lab.
Work Experience:
Advance Pharmaceutical Inc. 895, Waverly Ave, Holtsville, NY 11742 Date of Hire- Present
Position: Chemist
Job description:
• Performed all kinds of testing in QC lab i.e. raw materials, blend, finished product and blend study of
different times & rotation. Conduct process validation & stability testing of pharmaceutical product to
determine the viability under different environment condition.
Analyzed with laboratory instruments such as: HPLC, UPLC, LCP, UV, IR, Dissolution, DT, Titration, LOD, Karl
Fischer, Particle size, pH meter etc.
• Performed all kinds of tests specially assay, dissolution, content uniformity or dosage units, know &
unknown impurities of Sodium by carbonate, Calcium by carbonate, Ferrous Sulfate core and coated.
• Performed mineral test by ICP of Ca, Mg, Fe, Mn, Pb, Zn, Ni, Cu etc.
Feni Govt. College [2003-2011], Bangladesh.
Title: Assistant Professor & Lecturer (Chemistry)
Job description:
Facilitated undergraduate classes in chemistry and instructed undergraduate laboratory courses in general
chemistry and organic chemistry which include: pre-laboratory session, proctored examinations, critiquing
homework, lab report, quizzes and exams. Also designed a chemistry curriculum to assist college undergraduate
students in Organic & inorganic Chemistry.
UFFL (Urea fertilizer factory Ltd) [1997 July, 03 to September, 30] Bangladesh.
Job description: (Internship)
• Characterization of raw materials, synthesis catalyst, catalyst development, regeneration of catalyst,
acid quality & corrosion problem.
• Performed all kinds of tests especially assay, dissolution, content uniformity of dosage unite, known &
unknown impurities of different ingredients.
OSL (Opso Saline Ltd) [1996, July to December] Bangladesh.
Job description: (Internship)
• Performed all kinds of testing in QC lab, i.e. raw material, blend, finished product, conduct validation &
stability testing of pharmaceutical product to determine the viability under different environmental
condition.
• Performed preparation & standardization of VS & TS.
• Maintain all reports & data sheet according SOP.
• Performed disintegration, hardness, friability test.
• conducted various tests with osmosis & diffusion technology.
Computer Skill: MS Word, MS Excel.
Status: Permanent Resident Alien.
Educational Qualification:
Diploma in Analytical Chemistry and Green Building, From Cooper Union School of Engineering, New York, USA.
B.Sc (Honors) Dhaka University 1992-1996 in Applied Chemistry & Chemical Engineering.