Koladiya Vitthal
****, *.*. ******* ****• Jersey City, N.J 07307•m201-772-6812•
***************@*****.***
OBJECTIVE: Experienced Professional seeking to secure a position with a well established
organization with a stable environment that will lead to a lasting relationship in the field of
Pharmaceuticals.
SUMMARY OF QUALIFICATIONS
• Execution of daily / monthly production schedule by planning and making the most effective
use of available resources i.e. personnel, machinery in order to meet schedule & agreed upon
goals and objective.
• Identifying and taking action to improve quality, safety and efficiency of production process.
• Tracking of current work in process (WIP) products.
• Daily observation and audit of production floor for compliance with all regulatory requirements
(cGMP, SOP, Safety) and company’s policies.
• Regularly checking various equipment logbooks, daily observation records etc.
• Participate and lead in making process improvements.
• Prepared Training Matrix and Training Module for staff and worker and involved in training and
evaluation.
• Played major role during regulatory audits such as FDA, TGA, MHRA, and ANVISA.
• Being a part of Internal Quality Audit team responsible for internal plant inspection.
EDUCATION :
Keller Graduate School of Managemen
Master of Business Administration
Graduation Date: April 2010 GPA: 3.14
S .K.Patel College of Pharmaceutical Education & Research, India
Bachelor of Science in Pharmacy
Graduation Date: May 2003 GPA: 3.64
EXPERIENCE
Marg Pharmacy Inc. NY
Assistant Manager 06/2010 to Present
• Responsibilities as an assistant store manager include management of the schedules and
processes.
• Control the expenses, provide best customer service and train the employees.
Supervise display merchandising and maintenance of the store.
Torrent Pharmaceutical Ltd., India 4/2006- 3/2007
Senior Technical Assistant
• Motivated and guided staff of thirty, as well as provided timely performance recognition,
counseling and identified their training needs in various areas.
• Ensured employees participated and received all relevant training within required timeframes.
• Tracked department’s performance by preparing and reviewing daily and monthly reports.
Claris Life Sciences Ltd., India 2/2004-4/2006
Production Officer
• Managed staff of thirty five in manufacturing department.
• Participated and lead in making process improvements such as reduction of customer complaints,
product quality improvements and efficiency of man power.
• Suggested modification or corrections to the management if required and initiated change
requests to improve current practices through change control policies.
• Significant contribution made in projects involving reducing manufacturing cost, productivity
enhancement and continuous quality improvement programs.