Engineer Project

Objective: Seeking a full time or an Internship position as a Validation

and Process/Automation engineer for a Chemical, Pharmaceutical, Device

manufacturing, Biotech or R&D facility within an environment where I can

utilize and apply skills to develop my career, which involves application

of cGMP, ISO13485, 21 CFR parts 11, IQ/PQ/OQ, facility Inspection, OSHA.

Work specialties and area of Interest: Process and system automation

experience particularly DeltaV DCS and relevant other sub systems of

Emerson Process Management. More interested in areas such as Automation

system and data Validation, cGMP, FDA Compliance, IQ/PQ/OQ, Six Sigma

implementation and support.

Work experience: System Engineer / Executive with Emerson Export

Engineering Centre, India, from June 2005 - August 2008 (3

years and 3 months).

. Migration and System level design projects for different versions of

systems which include: Usage of basic Batch process, RS3, Fix32 to I

Fix, Provox, Upgrades from old versions of DeltaV to Newer ones.

. Graphics (GUI) configuration and testing, Faceplates and DFP's, Dynamo

configuration and testing: for above mentioned versions of automation

software, code debugging and support for customer queries as part of

standard procedures adopted.

. FAT and SAT support-on site project commissioning, assistance,

debugging and Implementation.

. Configuration with P&IDs, PFD's, and Customer provided materials like

DDS (detail design Specifications), configuration and testing of

process loops and customized logic configuration, testing.

. Various levels of experience ranging from Project execution and

Management, documentation, OSHA implementation, Queries,

Programming/application involving VBA, code debugging and support

(Upgrade projects-I Fix to IFix, NT to Xp or Vista), Alarms and events

management, Events Historian.

. Plant shutdown and startup activities and support, online testing with

DeltaV controllers.

. OPC mirror configuration, A&E server configuration, Field cabinet

testing, hardware wiring, Cabinet expansion and update, installation

and wiring support, loop communication tests.

. Visual Basic tools utilization, Profibus and Field bus testing, use of

AutoCAD for designing/modifications.

. In house configuration, checks and communication with customer or

third party for the offline or online testing and subsequent

debugging, design changes, handling design issues, other duties as

assigned.

DeltaV Assignment with AIV Solutions, LLC, NJ for a Project: GSK Bio-

fermentation:

Month of March 2010 (120 Engineering Hours):

. Graphics (GUI) configuration/ testing, new GUI checks, code debugging

and support for customer inputs as part of standard procedures

adopted. Configuration with P&IDs, PFD's. Dynamo replacement.

. Configuration checks and error spot checking for Unit procedures,

Phase classes and Equipment modules. Standard documentation as

required. Updated design specifications/ protocols for testing.

Specialization: Oil and Gas and refinery projects, Chemical plants and

Biotechnology, Pharmaceuticals.

Achievements: Project timely execution and good customer ratings for many

projects, good project charter management, successful implementation of

quality standards, project performance award.

Computer Skills: usage of 'C' programming, VBA, Matlab, LabView, Cadence,

Orcad, AutoCAD, assembly language programming, Hands on usage of: Windows

98 to Vista, MS Office and Access, tools and utilities usage, Inter and

intra office utilizes for software data sharing and communication, data

access.

Languages Known: Marathi, Hindi, English, French (passed Level 1 exam), and

Sanskrit.

Education: At Wayne State University, MI, Detroit: Completed M.S. in

Biomedical Engineering, August 2008 - May 2010 (Current GPA = 3.71/4).

. University of Pune, M.Sc., Instrumentation Science, University Rank

Holder, 2003 - 2005.

. University of Pune, B.Sc., Electronic Science, University Rank Holder,

2000 - 2003.

M.S. in Biomedical Engineering from Wayne State University:

Completed Masters Degree courses such as Business of Biotechnology,

Clinical Engineering,

. FDA-Drug and Devices evaluation with small test project in Stent

reconstruction, novel stent design with application of 21 CFR, IQ-PQ-

OQ standards, Manufacturing standards, Risk analysis, In vitro and In

vivo studies, Animal and Human studies, drug stability tests and

Investigations, PMS.

. Course work includes Human Physiology and Molecular Biology, Smart

Sensors - designing using Cadence software, Enabling Technology with

design enhancements, better facilities for Assistive living.

. Green Belt: Six Sigma Certification.

. Projects, activities performed:

* Algorithm for localization and multi dimensional scaling for

placement of different nodes in military or communication

applications.

* Developed a prototype for the ultimate web design with different

categories and classifications for Assistive technology and daily

living i.e. Activities of daily living, education, employment,

transportation and other sub categories.

* Seminar on 'Human Factor Engineering approaches in Clinical

Engineering'.

. Case Study: Indian Biotech major "Biocon"-analysis of products and

services offered, IND, NDA, Quality highlights, approved product

pipeline, Trends in Industry, cost effectiveness, R&D, IPO, Strengths,

protocols followed, benchmark and targets, Patents, Violations and

concerns, Acquisition and mergers, joint ventures and business

strategies, Risks and Investments, Social commitments.

. Currently working in area of bone, tissue engineering research Lab.

Experiment: Calcium polyphosphate deposition, bone repair,

cyclodextrin and PVA loading for the complex, RNA Synthesis.

Ready to relocate: anywhere in USA, outside USA for work and related visits

and References: Available on request.

Contact this candidate