To pursue a rewarding career with an organization that gives me an opportunity for taking on greater responsibilities, newer challenges, acquiring skills while providing an atmosphere for professional growth. Continual learner, able to easily grasp and implement new ideas and concepts. Ability to maintain good inter-personal relations. Highly energetic, enthusiastic and with an ability to achieve the targets even under pressure. Focused with determination and effective supervision.
Experience: A highly trained individual with approx. 17 years of experience ,excellent interpersonal skills, can manage workers issues and able to resolve effectively, proficient in computer skills which makes work faster, ability to meet deadlines, great attitude towards work and ensures all standards are met.
Compliance: Ensured compliance of various quality measures by appropriate requisite documentation/ records.
Current Industry: Pharma/ Manufacturing of Pharmaceuticals / Technical.
Current Location: Baddi (Himachal Pradesh) AUDIT FACED: International audit faced like USFDA, TGA, MHRA, WHO (Geneva), ANVISA and other audits like Uganda, Ukraine etc. AREAS OF EXPOSURE: Documentation / Quality compliance: Responsible for planning and review for the RM section. Responsible for QC functioning as per Regulatory aspects and maintaining QC compliance as per cGMP norms. Responsible for report and investigate the OOS, OOT, Atypical, Deviations, Incidents in the laboratory. Participates in troubleshooting laboratory instruments failure and provide proposals for improvements. Identifying and reporting critical & major quality and compliance Risks and gaps during audit activities. Review of Specifications, Standard Testing Procedures, Analytical Test Data Sheets and General test procedures. Instrumentation: HPLC Agilent attached with Chromeleon & Chemstation software. HPLC Shimadzu attached with Chromeleon & Class VP software. HPLC Dionex attached with Chromeleon software. HPLC Shimadzu attached with LC Solution software. HPLC Prominence attached with Chromeleon software. HPLC Waters attached with empower-2/empower-3 software. UPLC Waters attached with empower-2 software. U.V. Spectrophotometer (Perkin Elmer & Shimadzu 1700). Dissolution Tester (Electro Lab, Lab India). Disintegration Tester (Electro Lab) and other lab equipments like Refrectometer, Polarimeter etc.
Overview
1
1
Language
18
18
years of professional experience
Work History
Deputy manager in QC
M/s Oxalis Labs
09.2016 - Current
Working with M/s Oxalis Labs, Baddi as Deputy manager in QC from Sep 2016 to till date.
Sr. Officer in QC
SUN Pharmaceutical Ltd
01.2015 - 08.2016
Worked with SUN Pharmaceutical Ltd, Mohali as Sr. Officer in QC from January 2015 to August 2016.
Glenmark Pharmaceutical Ltd.
03.2012 - 01.2015
Worked with Glenmark Pharmaceutical Ltd. Baddi from March 2012 to January 2015
Fresenius Kabi Oncology Ltd
05.2010 - 03.2012
Worked with Fresenius Kabi Oncology Ltd (USFDA AND MHRA Approved plant) from May 2010 to March 2012
Cipla Ltd.
05.2008 - 04.2010
Worked with Cipla Ltd. WHO Certified plant. Baddi in QC from May 2008 to April 2010.
Education
Bachelor of Education -
University of Jammu
Jammu
Master of Science - Biochemistry
HNB Garhwal University
Srinagar
Bachelor of Science - CBZ
H.P. University
Shimla
Intermediate - PCB
HPBSE
Dharmshala
Matriculation - undefined
HPBSE
Dharmshala
Skills
Operating system: - Window 2010, Window XP
Accomplishments
Good Exposure in New Pharma Projects.
Control on Documentation.
DECLARATION:
I have a flair for learning new things and accepting challenges, I also have a realization and strongly believe that skill, determination, logical thinking and devotion, can prove to be an asset to any organization.