Highlights:

Skills:Method validation, Method verification and also involved in investigation

Scientist 04/15/2016 - current
Torrent Phrama Inc., Levittown, Pennsylvania United States
Industry: Pharmaceutical
Analytical method validation scientist
Responsibilities 1. Involved in method validation, method verification and method transfer for raw materials and liquid products 2. Analysis of stability products such as liquid, sterile and solid dosage form. 3. Qualitative and quantitative analysis of Bulk Finished and Stability sample by using HPLC and UV. 4. Identification test by UV and IR. 5. Qualitative and semi quantitative analysis by TLC. 6. Determine percentage release of dosage form by dissolution.--
Assistant Manager in Quality Assurance 09/2015 - 03/2016
Torrent Pharmaceuticals ltd, Indrad, Gujarat India
Industry: Pharmaceutical
Assistant Manager in Quality Assurance
Responsibilities 1. Section in-charge of Standard Testing Procedure (STP) and Protocol/Test Data Sheet issuance. 2. Responsible for audit compliance of both internal audit and external audit in quality control department. 3. Review of daily software audit trial and reconciliation of electronic file generated on workstation of instrument other than HPLC in quality control. 4. Review online work of analyst at work bench, i.e. review test data sheet regarding online reporting, verify glassware and interrogate with analyst regarding preparation. 5. Review of out-of-specification and out-of-trend test results with Department Head and initiate investigation.--
Software functional Head 05/2010 - 08/2015
Cipla Ltd., Prithampur, Indore, Madhya Pradesh India
Industry: Pharmaceutical
Software functional Head
Responsibilities 1. Review if Chromatography data, UV data and Stability protocol. 2. Review of daily software audit trial and maintain user management control to software in quality control regarding 21 CFR. 3. Review online work of analyst at work bench, i.e. review test data sheet regarding online reporting, verify glassware and interrogate with analyst regarding preparation. 4. Initiate investigation regarding Incidence, Out-Of-Specification and Out-Of-Trend 5. Qualification and calibration of instrument.--
Senior Officer 01/2009 - 04/2010
Sun Pharmaceutical ltd, Silvassa, Gujarat India
Industry: Pharmaceutical
Senior Officer
1. Reviewing of stability and calibration data. 2. Documenting work process and reporting in compliance with regulatory requirements. 3. Ensure that safe systems of work are practiced with due regards to Health and safety and Good manufacturing Practice. 4. Fundamental knowledge and experience about Out of specification 5. Checking and verifying data of other analysts as per GMP and regulatory standards.--
Senior Officer 08/2004 - 12/2009
Zydus Cadila Healthcare ltd., Ahmedabad, Gujarat India
Industry: Pharmaceutical
Senior Officer
Responsibilities 1. Analysis of various pharmaceutical products for development purpose. 2. In Vitro dissolution study of various pharmaceutical products. 3. Stability study as per ICH guidelines for different dosage form. 4. Documentation as per regulatory requirement. 5. Analytical method transfer to quality control--
Analyst 07/2001 - 07/2004
S Kant Healthcare ltd, Vapi, Gujarat India
Industry: Pharmaceutical
Analyst
Responsibilities 1. Involved in analysis of stability products such as liquid, sterile and solid dosage form. 2. Qualitative and quantitative analysis of medicines by using HPLC and UV. 3. Identification test by UV and IR. 4. Qualitative and semi quantitative analysis by TLC. 5. Determine percentage release of solid dosage form by dissolution and UV. 6. Concern in proper management of references and working standards for accuracy of analytical data.--

South Gujarat University, Gujarat, India 06/1995 - 04/2001
Valsad, Gujarat, India
Degree: Bachelor's Degree
Major:Chemistry
Minor:Physics
Analytical chemistry

Tarik Resume