Experience

Globyz Biopharma Services

• United States
• Biotechnology Research
• 1 - 100 Employee

• Director Global Business Development

  • Oct 2020 - Present

  Globyz Biopharma Services are End to End Service Provider of Comparators/ Princep (Small Molecule Therapeutics, Large Molecules, Products of Biological origin, Solid Orals, Injectables, Monoclonal Antibodies etc.). We specialise in HARD TO GET Princep and complete Clinical Trial Solutions. Clinical/Commercial Secondary Packaging, Labelling, Placebo Manufacturing for CT, Blinding/Randomisation, Clinical Trial Cold Chain Management, Speciality and Life Saving Medicine are some of our offerings. With Regulated Warehouses Spread across Canada, US, Brazil, UK & offices across Germany, USA, and Singapore, we can help our partner with unmatched reach and Best Quality in Services. Show less



Succor Pharma Solutions (Clinical and Formulation Development Consultant)

• Co-Founder

  • Dec 2018 - Present

  SUCCOR in French is 'Helping Hands', and I started this consultancy with an objective to help small/medium and virtual companies for their Product Development (Formulation, Clinical Development) needs. We are apt for your needs: 1. Identifying the right fit for the product (CRO Selection) 2. Negotiating the best quote. 3.Identifying the right source of API and raw materials. 4. Providing Project Management and technical hand holding during development. 5. Handling the entire Clinical Development (Identification of CRO-Clinical Development-Monitoring/Audit-CSR) 6. Handling of queries and CAPA management for both development data and Clinical phase etc. Show less


Epione Labs Private Limited
• India
• Pharmaceutical Manufacturing
• 1 - 100 Employee
• Head Of Business Development

  • Feb 2019 - Sep 2020


Jubilant Life Sciences Ltd.

• Business Development| GCLP| Data Integrity

  • Nov 2017 - Feb 2019

  Faculty trainer for GCLP, Data integrity, CGMP-CRO, ALCOA, BE data review, 21 CFR part 11, 210, 211.... Faculty trainer for GCLP, Data integrity, CGMP-CRO, ALCOA, BE data review, 21 CFR part 11, 210, 211....



RA Chem Pharma Ltd - India

• Deputy General Manager-Business Development & Project Management

  • Apr 2015 - Nov 2017

  CRBio is a full service CRO providing services for BA-BE, Clinical end point studies, Phase trials (I-IV), Statistical Services and Data Management. Inspected by USFDA, WHO-Geneva, UKMHRA, BPFK, MOH-Turkey and MOH-UAE. CRBio is a full service CRO providing services for BA-BE, Clinical end point studies, Phase trials (I-IV), Statistical Services and Data Management. Inspected by USFDA, WHO-Geneva, UKMHRA, BPFK, MOH-Turkey and MOH-UAE.



Laboratories GENPHARMA

• Morocco
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• • Oct 2011 - Mar 2015

• • Aug 2009 - Oct 2011

  Head Bioanalytical, Involved into the technical and operational aspects of running a BA Lab.



Jubilant Clinsys

• United States
• Research Services
• 100 - 200 Employee

• Project Leader Bioanalytical

  • Jan 2007 - Aug 2009

  Various administrative functions, including project management, audit from external regulatory bodies and many more. Also review of the Bioanalytical data. Various administrative functions, including project management, audit from external regulatory bodies and many more. Also review of the Bioanalytical data.



Glenmark Generics Ltd.

• Senior Research Officer

  • Jul 2006 - Jan 2007

  Method Development for the Drugs for the Quantitative Estimation in Biological Matrix. Bioanalytical Method Validations. Documentation of the Developed Methods, Method Validations and Bioequivalence Studies as per SOP. Overseeing the ongoing Bioanalytical studies are completed on the given time lines. Formulation of SOPs covering various aspects of Bioanalytical lab in conformation with regulatory guidelines , their periodic revision and organizing in-house training on SOP'S and other technical updates. Review of the study reports. Review for some of the Glenmark sponsored project in CRO's. Overall review of the system and building up a system in accordance with the regulatory requirements, working in close proximity with the QA group on the various aspects of a GLP and their implementation. Show less



Ranbaxy

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Research Scientist ( Ranbaxy Research Limited)

  • Mar 2003 - Jun 2006

  Development of the LCMS/HPLC method into the Biological matrix. Validating the developed methods. Bioanalysis of the samples. Development of the LCMS/HPLC method into the Biological matrix. Validating the developed methods. Bioanalysis of the samples.



HAMDARD UNIVERSITY

• Pakistan
• Higher Education
• 700 & Above Employee

• • 2001 - Mar 2002

  Research title:Extraction, Isolation and Characterisation of the extract from Embelia Ribes.CNS protective activity of the drug was also studied extensively using animal model.

• • 1996 - 2002

  Graduation and Post graduation