Maimuna H. Email & Phone Number

London, Gb

London, Gb

Basildon, England, United Kingdom

Ware, England, United Kingdom

Ware, England, United Kingdom

Authored Laboratory Analytical Method, Authored and updated SOPs, WI, Job Aids. Reviewed Pharmacopoeias like USP, Eur. Ph, BP. supported other controlled documents and authored in house compliance documents.

Ware, England, United Kingdom

Karāchi, Sindh, Pakistan

• Head of Department - Chemistry.• British curriculum.• Created interesting and educational experiments to capture students’ imaginations.• Prepared daily lesson plans and scheduled engaging classroom activities.• Liaised with parents to encourage continued learning at home.• Set realistic goals for students and tracked progress.• Administered practice exams to enhance students’ skills.

Riyadh, Saudi Arabia

• Taught chemistry and physics to higher grades (O/A Level)• American curriculum.• Preparing session, semister, weekly and daily lesson plans.• Taught students using various methods including presentations and projects.

Karāchi, Sindh, Pakistan

• Performed finished product and stability sample testing using HPLC, UV/VIS spectrophotometric analysis.• Performed blend uniformity, assay, content uniformity, residual solvents, dissolution, TLC, FTIR, and water determination offinished product and stability samples.• Performed all job responsibilities in safe and efficient manner.• Released product before deadline.• Trained other personnel in analytical instrumentation, test methodology and auditing the analytical… Show more • Performed finished product and stability sample testing using HPLC, UV/VIS spectrophotometric analysis.• Performed blend uniformity, assay, content uniformity, residual solvents, dissolution, TLC, FTIR, and water determination offinished product and stability samples.• Performed all job responsibilities in safe and efficient manner.• Released product before deadline.• Trained other personnel in analytical instrumentation, test methodology and auditing the analytical work.• Performed LIR investigation as needed. Followed corrective action and preventing action to eliminate the cause of non- conformities. Show less

Karāchi, Sindh, Pakistan

• Performing the analytical method evaluation, method development, raw material, finished product, cleaning agent and cleaning validation of carryover from previously run product on pharmaceutical equipment.• Performing qualitative and quantitative analysis of raw material, finished product, stability, process validation, and cleaning validation sample-using analytical instrumentation such as GC, UPLC, HPLC, TLC, UV/VIS Spectroscopy, pH meter analysis, particle size analysis, Karl Fischer… Show more • Performing the analytical method evaluation, method development, raw material, finished product, cleaning agent and cleaning validation of carryover from previously run product on pharmaceutical equipment.• Performing qualitative and quantitative analysis of raw material, finished product, stability, process validation, and cleaning validation sample-using analytical instrumentation such as GC, UPLC, HPLC, TLC, UV/VIS Spectroscopy, pH meter analysis, particle size analysis, Karl Fischer, FTIR, wet chemistry, etc.• Auditing/Reviewing the routine analytical work such as QC release, stability testing, method validation, cleaning validationperformed by another analyst. (Peer review)• Have in depth knowledge of chromatographic analysis such as tailing factor, resolution, peak purity, purity angle, purity threshold, capacity factor, theoretical plate count, chromatographic peak. As a professional chromatographer, troubleshoots the instruments, method development challenges and routine LIR investigations.• Serving on a laboratory committee such as safety, suggestion, cGMP, SOP, and news latter.• Maintaining laboratory notebook as per the FDA regulation and cGMP requirement.• Performing other duties as assigned such as product technical package and specification evaluation.• Performed finished product and stability sample testing using HPLC, UV/VIS spectrophotometric analysis.• Performed blend uniformity, assay, content uniformity, residual solvents, dissolution, TLC, FTIR, and water determination offinished product and stability samples.• Performed all job responsibilities in safe and efficient manner.• Released product before deadline Show less

Masters Of Science - Msc, Pharmaceutical Science With Management Studies

Master’s Project: Synthesis of Sugar-Responsive Polymers using Reversible Addition-Fragmentation Chain Transfer RAFT for the treatment.

B.Sc (Hons.), Chemistry, 4 Gpa

Inorganic Chemistry, Organic Chemistry, Physical chemistry, Biochemistry, Biostatistics

Masters Of Science - Msc, Analytical Chemistry, 3.5 Gpa

Course module in Analytical Chemistry: Molecular and atomic spectroscopy, Separation science, Specialized Analytical Techniques, Data.

Master'S Degree, Analytical Chemistry, 1St