Mellcon Engineers Pvt Ltd Delhi : QA QC Quality Assurance

[Admin]

Mellcon Engineers Pvt. Ltd.
http://www.mellcon.com

Keywords: QA QC Engineer, QA, QC, QA QC Engineer Mechanical production fabrication

Designation: Engineer QA, QC Quality Assurance
Experience: 3 - 7 Years
Location: Delhi
Education: UG - B.Tech/B.E. - Mechanical,Diploma - Any Specialization
PG - Any PG Course - Any Specialization,Post Graduation Not Required
Industry Type: Industrial Products/Heavy Machinery
Functional Area: Production, Maintenance, Quality
Posted Date: 31 Oct 2008

Job Description
1. Preparing & Maintaining all quality documents like QAP /QCP plans, raw material , in process test reports & final documentation

2. Preparing of QA/QC procedures, QA plan, welding inspection RT, NDT like DP Test hydrotest for Pressure Vessels , Heat Exchangers & related Eqpts. Should have welding certificate AWS, CSWIP & NDT Level II Preferably.

3. Coordinate with client's / Consultant representative for QA/QC activities during approval & Inspection etc.

Desired Candidate Profile
Degree / Diploma in Mechanical / Engineering with 3-10 years experience in Quality Assurance / Quality Control in Industrial Equipments Fabrication Industry, process plant manufacturing like boilers, Pressure vessels, heat Exchangers, Water treatment plants.pumps , compressors etc. Should be proficient in preparing plans and work procedures and familiar with relevant ASME & IS Standards & Codes Interpretation.

Company Profile
Mellcon Engineers Pvt. Ltd. is a closely held Company. It has Production units in Okhla Industrial Area New Delhi, India manufacturing a complete range of Compressed Air & Gas Dryers, Water/Brine/ Refrigeration Chillers, Cold Rooms Equipments & Walk in coolers , PSA Nitrogen Gas Generators.

The Company's products are approved by NTPC, BHEL, EIL , TOYO etc.

The company has also been accorded ISO-9001-2000 certification by BSI.

Executive Name: Director - HRD

Address:
Mellcon Engineers Pvt Ltd
Mellcon Engineers Pvt. Ltd.
B-297, Okhla Industrial Area, Phase - I
New Delhi - 110020
Delhi,Delhi,INDIA 110020

Email Address: jobs@mellcon.com

Telephone: 91-011-26816103

[Guest-IJT]

Trupti Patil
trupti.patil01 AT gmail.com
Quality Assurance

Ms. TRUPTI ASHOK PATIL.
Tal.- Karad Dist : Satara.
Maharashtra.
trupti.patil01 AT gmail.com

CAREER SNAPSHOT
Seeking position in an organization where I can apply my thoughts and skills for the development of the organization as well as my personal growth.
EXPERIENCE DETAILS
- Working in Quality Assurance as management staff in Cipla Goa Unit III, Plot No.L-143 and L-144, Verna Industrial Estate, Salcette, Goa –403722 from date May24, 2007 to till date.
- Worked in a Quality Control Department as QC Executive for Six month in Lupin Limited, B-15, and phase 1A Verna Industrial Estate, Salcette Goa -403722. from date November 23, 2006 to May22, 2007.
- Worked in a Quality Control Department for two and half year as a Section Head in Okasa Pharma (Cipla Ltd.) Private limited,L-2 additional MIDC area Satara -415004 from date March 05, 2004 to September 02, 2006.
- One and half month in plant training in Mediorals Labs. Pvt. Ltd . , J-4/2 Additional MIDC, Satara – 415004.
SPECIAL ACHIVEMENT
- FDA Approval in Chemical and instrumental analysis.
ACADEMIC DETAILS
Examination Institute / University Year Percentage
Advance Diploma in Pharmaceutical Quality Assurance Management Institute Of Pharmaceutical Education and Research, Pune. (Maharashtra).
09.10.2006 56.00%
Maharashtra state Certificate in information Technology Maharashtra State Board of Technical Education, Mumbai. 05.01.2005 83.75%
B.Pharmacy Satara College of Pharmacy, Nigadi,
Dist-Satara, Shivaji University, Kolhapur (Maharashtra)
31.12.2003
65.75 %
COMPUTER SKILLS
Knowledge of MS Office, Power point Excel, Internet operations.
CO-CURRICULAR ACTIVITIES
Participate in 54 th Indian Pharmaceutical Congress 2002.
JOB RESPONSIBILITIES
1. Job Profile in Okasa Pharma ( Solid and injectable Dosage form) :
- Instruments Handled :
o HPLC : Shimadzu, TSP, Agilent, Dionex
o GC : Chemito 8610 HT, Perkin Elmer
o TOC : Shimadzu (TOC VCSH)
o IR : Shimadzu (FTIR 8300)
o Melting Point : Lab India
o Dissolution Test Apparatus : Lab India, Electra lab.
o Autotitrator : Methrohm.
o KF Coulometer : Methrohm
- Qualification, Calibration, and SOP of Instrument and Equipment.
- Preparation of the working standards and Test standards.
- Testing of Validation, Raw Material, Finished Products, and Stability Samples.
- Audit Faced : FDA Inspection, WHO, TGA.
2 Job profile in Lupin Ltd ( Solid Dosage form) :
- Instruments Handled :
o HPLC : Dionex
o GC : Perkin Elmer
o TOC : Shimadzu (TOC VCSH)
o Melting Point : Lab India
o Dissolution Test Apparatus : Lab India, Electra lab.
o Autotitrator : Methrohm.
o KF Coulometer : Methrohm
- Qualification, Calibration, and SOP of Instrument and Equipment.
- Preparation of the working standards and Test standards.
3 Job profile in Cipla Unit –lll Goa ( Solid Dosage form) :
- Creating and Handling quality system and procedure.
- Fulfillment of current needs of Training with respect to cGMP, GLP and GEP.
- Handling of Complaint, Deviations ,Change Controlsand CAPA.
- Participate in investigation of deviation, Complaints and out of specification test result.
- Establish and approval process validation and cleaning validation programme.
- General document preparation including Product History File, APQR, Flow sheet, Master protocol and report.
- Batch Record review.
- Rejection Handling.
- Dossier review and ensuring the sourcing of material, manufacturing and testing is carried out as per dossier.
- Co-ordination with RA for the document required by them for purpose of registration.
- Risk assessment: FMEA.
- Self inspection of all departments.
- Audit Faced : MCA, MCC, FDA Inspection, WHO,TGA,USFDA,MHRA .
TRANING ATTENED

- Training attended of Dr. Nilgel Halls , UK, GMP, Consultant, Australia on different topics such as Microbiology Aspects of Cleaning Validation , Detection of Objectionable Microorganism, Investigation of Microbiology failure ,Identification of Microorganisms media fill , Changes of FDA etc.
- Training attended of Mr. Derek Smith, GMP, Consultant, Ex.Inspector, TGA, Australia on Cleaning validation.
- Training attended of Michael Ansifiled Director of Globepharm on Risk Management, OOS Investigations and CAPA, Global Regulatory Affairs.
- Training attended of Dr. Nrapentra Nath Avenue, a Grange Park on Sterility Assurance review.
- Training attended of Mr. Destin LeBlanc on Cleaning validation.
- Training attended of Kent Faul Lachman Consultant, Services Inc on Best Practices in performing effective investigation for OOS results and extraneous peak to meet current FDA expectation.
- Training attended of Ziva Abraham , Micro rite, Inc on Microbiology laboratory practices.
- Training attended of Randy Hutt ,Lachman Consultant, Services Inc on Aseptic Processing an Investigation in Aseptic processing
CTC
Current : 5.0 lac per Annum.
Expected CTC : 7.0 to 8.0 lac per Annum Negotiable


Ms. Trupti A. Patil
Date
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Place
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