• Gender: Male
• Age: 54
• Designation: Manager
• Highest Education Level: Post Graduate Diploma
• Current Gross Salary: INR  425000 /Annum
• Preferred Country: India
• Preferred Location: Anywhere
• Work Experience: 29.4 Year(s)

Education

Pursuing M.B.A. from P.T. University, Patiala (Punjab)
Master degree in Science (M.Sc.) with Chemistry from M.P. Bhoj University Bhopal (M.P.) in 2007.
Bachelor degree in Science (B.Sc) with Chemistry, Physics and Maths from A.P.S. University Rewa (M.P.).
L.L.B. from A.P.S. University, Rewa (M.P.) in 1995.

Skill Sets

Quality Assurance.

Work Experience

Manager - QA & QC
Since March 2008 to till date.
Presently working with a leading medical device manufacturer

Manager - Quality Control in CGMP
Since April 2006 to February 2008
Worked with M/s Lyra Laboratories Pvt. Ltd., Barotiwala Distt., Solan (HP)

Senior Officer - Quality Control
Since January 2004 to March 2006
Worked with M/s Charak Pharma Pvt. Ltd., Baddi Distt., Solan (HP).

Analyst - Quality Control (Incharge)
Since November 1997 to January 2004
Worked with M/s Maharishi Ayurved Corp. Ltd., Faridabad (HR).

Junior Chemist (Quality Control)
Since August 1995 to November 1997
Worked with M/s Dee Pharma Pvt. Ltd., Sikandrabad, Distt. Bulandshahar (UP).

Job Responsibility:
Independently handling complete quality control and quality assurance from Raw material to
finished Product.
To manage and assist with all requirement of QC lab and day to day working
Reporting to Director.
Job Profile:
Preparations of Master Formula record and BMR & BPR according to regulating authorities.
Validation Protocol for process validation, cleaning validation, Method validation according to regulating authorities.
Routine analysis of raw material semi-finished and finished product viz Tablet, Capsule, Oral Syrup, Oral Dry Suspension, Sterile Ophthalmic product (Eye Drops), and External application (Ointment & Lotion) as per IP, BP, USP & IH specification and their record as per WHO cGMP & ISO 9001.
Handling the different types of instrument like HPLC, UV Spectrophotometer, FTIR, Brookfield viscometer, TLC, Karl- Fischer Titrimeter, Potentiometer Auto titrator, Polarimeter, Melting point App., Refractometer, Friability test app., Bulk Density app., Bursting Strength app. and their Calibration record as per GMP & ISO 9001.
Approved technical person for analysis from FDA Shimla (HP).
Analysis of ETP, Soft, WFI, Purified and drinking water as per IS 10500 standard & IP.
Handling of analysis related to market complaint and comparing the same with the control sample as per GMP specification.
Preparation of SOP & STP for finished product, Raw materials and Packing Material as per GMP & WHO.
Preparation of SOP for Laboratories instrument as per GMP & ISO.
Analysis of Packaging material viz. Label, Carton, Catch cover, Corrugated box, Plastic Containers, PVC & PVDC, Blister foil, Glass bottle and Aluminum Collapsible tube etc.
Preparation of Calibration and Validation formats as per GMP & ISO.
Participate in ISO 9001 auditor training program and successfully completed.
Documentation as per GLP, GMP and ISO 9001.

Future Goals

Desirous of working with a company which can offer me a unique opportunity to learn and grow with and within organization and exploit my potential to the fullest.