www.cosmicbschool.in Cosmic Academy Delhi : Web Developer / Web Designer

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Cosmic Academy
http://www.cosmicbschool.in

Cosmic Academy : Delhi : web developer / web designer

Keywords: web designer web developer

Company Profile
Cosmic Business School is a center of excellence in management imparting UGC recognized postgraduate and undergraduate programs in Management and computer application. The institute is also affiliated to All India Management Association (AIMA)

web developer / web designer
Experience:
1 - 6 Years
Location:
Delhi/NCR
Compensation:
Rupees 1,00,000 - 2,00,000
Education:
UG - Any Graduate - Any Specialization;Graduation Not Required

PG - Any PG Course - Any Specialization;Post Graduation Not Required
Industry Type:
Education/ Teaching/Training
Functional Area:
Web, Graphic Design, Visualiser
Posted Date:
16 Sep


Job Description
Responsible for Website designing and development.

Desired Candidate Profile
He should have knowledge and work exp in
1.ASP
2. JSP
3. PHP
4. My Sql
5. SQL
6. Adobe and Corel.

Executive Name:
HR

Address:
Not Mentioned

Email Address:
hr@cosmicbschool.in

Telephone:
Not Mentioned

Reference ID:
web designer / HR/ 07

[Guest-IJT]

Name : Anand Ingole
Email : ingoleanand AT gmail.com
Designation / Skillset : Manager Quality Assurance
Dear Sir,
With reference to Mr. Patil, I am enclosing herewith my
resume for your perusal.
I would like to express my interest in a position as “Manager Quality
Assurance or Quality Control of your organization. I have total 25
years of experience in QA & QC department with strong administrative
skill.
Thank you so much for your time & consideration.
Sincerely
Anand Ingole

Resume :

A Pharmaceutical Quality Assurance professional with 25+ years’ experience from India and UAE. Currently working as Manager, Quality Assurance and Quality Control at Neopharma, LLC, Mussafah, Abu Dhabi since October 2010.
Professional Synopsis
1. Total 25+ years’ experience in analysis of Pharma Quality Control and QMS; out of which 11 years are at Manager’s level.
2. Presently working at Neopharma, LLC in Mussafah, Abu Dhabi as Manager –Quality Control from 25th of October 2010.
3. Guidance to Management of Pharmaceutical Quality Control Laboratories and Quality Assurance departments.
4. Support to Regulatory department both for export dossiers, QA audits, Validation related issues.
5. Developing entire systems of control in Quality Control lab, personnel training and QC documentation per GMP/GLP regulatory requirements
6. Guidance to developing systems related to Calibrations, Qualifications and Validations of analytical instruments such as pH meter, DT Apparatus, Dissolution Apparatus, Refractometer, Polarimeter, Bulk density apparatus, TLC, conductivity meter and sophisticated instruments like UV-VIS spectrophotometer, Gas Chromatography, HPLC and FTIR.
7. Accredited as an expert staff for Chemical, Instrumental and Microbiological testing by state Food and Drugs Administration.
8. Conducting Plant and Quality Audits in accordance with guidelines of WHO-GMP, MHRA, TGA, ANVISA & AFSAPS for Pharma formulations.
Previous job at Cipla LTD., Unit-IV, Verna–GOA, India.
Designation : Management Staff
Period : From September 2010 to October 2010
JOB PROFILE
Quality Control :
Overall in charge for cGLP compliance, day-to-day activity & Quality issues
Previous job at ENCUBE ETHICALS PVT. LTD., Madkaim, Ponda –GOA, India.
Designation : General Manager - Quality Control
Period : From April- 2009 to September 2010
JOB PROFILE
Quality Control :
To coordinate with loan licensee parties for day-to-day activity & Quality issues.
- Operation, Calibration & Trouble Shooting of modern Pharma analytical Instruments such as UV-VIS Spectrophotometer, HPLC, GC, FTIR, FTNIR, AAS, Autotitrator etc.
- Analytical Methods Development and validations
- Microbiology study (MLT, Assay, Environment Control, & Water, PET and support to validation studies)
- To conduct internal training, audit & analyst’s validation
- To evaluate OOS & OOT in routine practice
- To implement Good Laboratory practices in all QC functions
- Maintain and prepare Reference as well as Working standard
- To implement sampling instructions, specifications, test methods & other QC procedures
- Raw material & Packing material vendor audits
- Contract laboratory audit
- Successfully faced ANVISA Brazil & AFSAPS France audit
Past Experience :
1. Served in BLUE CROSS LABORATORIES LTD. Verna, GOA.
Designation : General Manager Quality Assurance
Period : From July- 2003 to March 2009
Quality Assurance
- Preparation, review and implementation of all ‘Standard Operating Procedures [SOPs]’.
- To prepare & maintain Master Document,
VMP, Site Master, Self-Inspection, Training Manual, Process Deviation, Change Control,
NCR, FIR, Annual Product Review, Market Complaint & Product Recall.
- Well versed with Validation,
Process, Equipment, Cleaning, HAVC, Water, Environment & Analyst.
- Raw material & Packing material vendor audits.
- Implement Good documentation practices w.r.t. Specs / STPs / SOPs / Protocols / BPR.
- To evaluate Good Warehouse practices for control & storage of RM/PM/FP.
- Monitoring & Execute Stability studies as per regulatory requirements.
- Review of batch manufacturing records, compliances & Approve/Reject batch for sale.
- Knowledge of Regulatory guidelines
- Preparation, review and implementation of ‘Standard Analytical specification’ for raw material, In-process Samples, Packing material, and finished product.
- To implement self inspection program & ensure all time readiness for external audits.
Production
- Process scale up in coordination with formulation development, production & technology
transfer documents.
- Preparation & implementation of Batch Manufacturing / Packing Record [BMR/BPR]
- Preparation of Master Formula Cards.
- Production equipment cleaning & stress study validation.
- Monitoring & execute the process validation.
- Shop-floor quality assessment and compliance to production SOP on day-to-day basis.
- Brief idea of process of formulation in dosage forms & External preparation.

Quality Control
- Operation, Calibration & Trouble Shooting of Advance Instrument,
HPLC, GC, FTIR, Autotitrator & UV-VIS Spectrophotometer.
- Analytical Methods Development.
- Microbiology study (MLT, Assay, Environment control & Water)
- To conduct internal training, audit & analyst validation.
- To evaluate OOS & OOT in routine practice.
- To implement Good Laboratory practices in all QC functions.
- Maintain and prepare Reference as well as Working standard.
- To implement sampling instructions, specifications, test methods & other QC procedures.
- Raw material & Packing material vendor audits.
- Contract laboratory audit.
2. Served in CFL Pharmaceuticals Ltd.( CMM Group of Company), Ponda, Goa.
Designation : Manager QA
Period : February- 2001 to June 2003
Developed Quality Control Department in a defined manner.
- Initiated and established Q C system, which include total documentation related to GLP practices,
- Qualified the areas, modified man movements and material flow
- Number of analytical Methods developed for new products by using HPLC, UV-VIS and Gas
chromatograph.
- Prepared validation master plan of Instruments for Calibration.
- Stability study master plan for existing and new formulations.
- All working standards developed for API.
- Conducted in house GLP training programs.
- Prepared ISO 9001-2000 Certificates documentation.
- Successfully faced audits of WHO- GMP (Geneva- Auditors) & ISO.

Achievements :
- Successfully handled the WHO-GMP inspection of Small volume injectable and
ISO- 9001- 2000 certificate audits.
3. Served in Encube Ethicals Pvt. Ltd. Madkaim, Goa
Designation : Asst. Manager QA
Period : November - 1999 to January – 2001
Developed Quality Assurance and Quality Control Department in a defined manner
- Initiated and established Q.A. system, which include total documentation related C GMP practices, document control, IPQC activities.
- Prepared validation Master plan, prepared and executed validation protocols.
- Qualified the areas, modified man movement and material Implemented upgraded Batch Manufacturing records.
- Conducted In house training programs.
- Prepared Raw Material , Packing Material and Finished products specifications.
- Successfully launched 45 products of Ointments with validation.
- Stability testing
- Validation of cleaning procedure.
- Analytical Method Validations
Achievements :
Successfully handled WHO, M/s Aventis Pharma International audit, M/s Galderma
France audit.
4. Joined Ranbaxy Labs Ltd. Pune in 1994 as QC Executive. Served for 5 years.
The significant contribution included laboratory management systems and system improvement in Quality Assurance though Gap analysis, internal audits of warehouse, plant and laboratory.
- Calibration of Instruments
- Preparation of Working standard and reference standards
- Stability testing
- Microbiological analysis.
- Process validations
- Validation of cleaning procedure.
- Analytical Method Validations
- SOP’s Preparations
- Documentations as per TGA and MCA requirements.
- Analysis of Raw Materials, Finished Products and Packing Materials
Achievements : Presented relevant documents as requested by the TGA, MCA and WHO
Inspectors and accompanied during factory inspection Got WHO-GMP, TGA and MCA.
Got approval of Expert staff in Microbial testing by Maharashtra FDA Pune division.
5. Started career with Li Taka Pharmaceuticals Ltd, Pune as QC chemist in Oct. 1986 to Nov 1994 Served for 8 years.
Learned basics of analytical testing techniques typical Pharma dosage forms like Tablets, Capsules, Liquid orals and powders. This included analysis of raw and packaging materials, In-process testing, testing of Finished products and Stability study.
Participation and significant contribution in the system development in QC lab led to promotion to QC executive level.
- To analyse packing Materials
- To analyse raw material analysis
- To Calibrate UV-VIS Spectrophotometer, HPLC and FTIR
- Analytical Method developments.
- To monitor all Quality control Activities.
- Stability testing
- Analysis of Loan Licence products analysis.
- SOP’s Preparations
- Training to QC Officer.
Achievements : Presented relevant documents as requested by the MNC’s Auditors
and accompanied during factory inspection.
Got approval of Expert staff in Chemical and Instrumentation by Maharashtra FDA Pune
division.

Qualification :
B. Sc. (Chemistry)-First Class
Advance Diploma in Analytical Chemistry- First Class
M.Sc. - First Class.
Date of Birth : June 1, 1962.
Family Background :
Married- House wife
1 sons - Studding ( 2nd year Diploma in Computer Engineering)
1 daughter- Studding ( X- STD )
Passport Details : F8419127, Date of Expiry: July 18, 2016.
ANAND INGOLE
July 22, 2011
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More Information about this submission and submitter:-
___________________________________________________
Submission ID : 4445308
Date & Time : 4th Aug 2011 2:49 PM (UTC)
IP Address : 117.212.180.72
Browser Info : Mozilla/4.0 (compatible; MSIE 8.0; Windows NT 6.1; WOW64; Trident/4.0; GTB7.1; EasyBits GO v1.0; SLCC2; .NET CLR 2.0.50727; .NET CLR 3.5.30729; .NET CLR 3.0.30729; InfoPath.2; .NET4.0C)
Predicted Country : India