Ajhar Hussain Email & Phone Number | Have expertise in Stable, Robust, Cost effective, Bioequivalent Formulation Development for dosage forms like Immediate Release Tablets, Delayed Release Tablets/Capsules, Modified Release Tablets, Dry Powder for Suspension. Extensive experience in formulation and process development of oral solid dosage forms. Excipients compatibility, formulation screening and prototype development to support early phase clinical studies through to further optimisation of formulation and manufacturing process to support late phase 2/3 clinical trial supplies and ICH stability programmes in a GMP facility. Technology transfers of late stage development projects to include a review of technical package, performing gap analysis, quality risk assessment, planning and execution of tech transfer batches to support site stability and registration batches. Review of project proposals including strategic and technical discussions with clients to establish project scope, timeline and key deliverables. URSs, Vendors selection, FAT and SAT

Ajhar Hussain

Have expertise in Stable, Robust, Cost effective, Bioequivalent Formulation Development for dosage f...
Gillingham, England, United Kingdom

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Ajhar Hussain’s Location Gillingham, England, United Kingdom

Ajhar Hussain’s Current Industry Recipharm Recipharm Queenborough

Ajhar Hussain’s Prior Industry Watson Pharma Mumbai | Dr Reddys Lab | Watson Pharma

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Senior Formulation Scientist

2021-12-01 00:00:00 - Present

Senior Formulation Scientist

2021-12-01 00:00:00 - Present

Executive Formulation R&D

2011-01-01 00:00:00 - 2013-02-01 00:00:00

Jr. Manager

2009-08-01 00:00:00 - 2010-12-01 00:00:00

Formulation Officer

2007-01-01 00:00:00 - 2009-08-01 00:00:00

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Ajhar Hussain is a Have expertise in Stable, Robust, Cost effective, Bioequivalent Formulation Development for dosage forms like Immediate Release Tablets, Delayed Release Tablets/Capsules, Modified Release Tablets, Dry Powder for Suspension. Extensive experience in formulation and process development of oral solid dosage forms. Excipients compatibility, formulation screening and prototype development to support early phase clinical studies through to further optimisation of formulation and manufacturing process to support late phase 2/3 clinical trial supplies and ICH stability programmes in a GMP facility. Technology transfers of late stage development projects to include a review of technical package, performing gap analysis, quality risk assessment, planning and execution of tech transfer batches to support site stability and registration batches. Review of project proposals including strategic and technical discussions with clients to establish project scope, timeline and key deliverables. URSs, Vendors selection, FAT and SAT