
Timeline
Skills
GmpPharmaceutical industryPharmaceuticsRegulatory affairsFormulationDissolutionSopHplcDrug deliveryStandard operating procedureGlpUvU.s. food and drug administrationTechnology transferPharmaceutical researchAbout me
Formulation and development of Solid Oral Dosage Forms (ANDA/MAA) - Tablets, Hard gelatin Capsules For US and Europe Market. Strong community and social services professional with a Master's Degree focused in Pharmaceutics from NDMVP's College of Pharmacy (CPN) Nashik.
Education

College of pharmacy, nashik
2010 - 2012Master's degree pharmaceutics
Satara college of pharmacy
2003 - 2005D. pharmacy pharmacy
Shree deshikendra vidyalaya, latur
1990 - 2000
Shivlingeshwar college of pharmacy, hasegaon, tq. ausa
2005 - 2009Bachelor of pharmacy - bpharm pharmacy distinction
Experience

Gsk
Jun 2012 - Jun 2013Research traineeResearch training at “GlaxoSmithKline" Pharmaceutical Research and Development Center, Nasik involved Packaging Development Project titled stability evaluations of water soluble vitamins with minerals in different primary packs.

Mylan
Aug 2012 - Apr 2014OfficerInvolved in shop floor day-to-day production activities, handling of equipment's, ensure maintenance of cGMP, ensure implementation of SOPs and work allocation.Key role in managing Production target in given shift.Filling of BPCR and review of BPCR. Initiation of Change control and DeviationsAllocation of manpower in a shift and working with team.Part of team in various regulatory body’s audits.To co-ordinate with other departments related to complete given job.

S.zhaveri pharmakem pvt. ltd.
Apr 2014 - Apr 2016Research associate -iWorking as a Research Associate-I in Formulation Development Department of Crontract Research organisation For Regulated Market (Europe and US) in Oral Solids. Literature search through internet,journal,Patents,FDA official websites.Innovator product characterization and reverse engineering.To assists Pre-formulation and compatibility studies prior to the formulation studies.Design and Execution of lab scale trials for product development in consultation with senior.Interpretation of analytical lab tests results to support development work.Stability study as per ICH guideline, stability data compilation and interpretation.Packaging Development.Preparation of compatibility study protocol, stability testing protocol along with technical documents like Product development report (PDR), Master Formula record (MFR). Show less

Enaltec labs pvt ltd
Apr 2016 - nowResearch officer
Licenses & Certifications

Registered pharmacist
Maharashtra state pharmacy council - india
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