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Training Analyst

Location:
Mumbai, MH, India
Salary:
60,000 US dollar p.annum
Posted:
September 08, 2013

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Resume:

CAREER OBJECTIVE

Incessantly striving for the knowledge acquisition and take up more

challenges for achieving excellence of the organization with my strong

determination and knowledge besides my individual growth.

Quest for challenging job that provides more opportunities to grow to

take up more responsibilities with independent decision making environment

that requires utilizing my skills and abilities.

ACADEMIC QUALIFICATION

* M.SC (IND. Chemistry) from Deptt of Chemistry VNSGU Surat (2005-2007)

* B.Sc (IND. Chemistry) from Rofel college Vapi affiliated to VNSGU

Surat (2002-2005)

* Intermediate (Science) from Upasana Lions English school Vapi,

affiliated to GSEB Gujarat,(2001-2002).

* S.S.C from Upasana Lions English School Vapi, affiliated to GSEB

Gujarat

( 1999-2000).

TECHNICAL QUALIFICATION

* Pursuing MBA from IGNOU Open University.

* Pursuing Graduate Diploma in Packaging from IIP Hyderabad.

* Diploma in Web Designing from NIIT Vapi Gujarat in 2004.

* Attended Internal Auditor Training Programme for ISO 9001: 2000, QMS &

ISO 19011 Part I, II, III for Audit Management from ICS Technologies.

PROFESSIONAL EXPERIENCE :

* Serving pharma formulation industry from more than 6 years

specifically in Packing material linked overall activities from

start to end with full regulatory compliance and full co-operation

to other all linked departments such as Regulatory,PRD,Production

etc and achieve company goal.

* Presently working in Aurobindo Pharma Ltd Unit -IV Injectable

Formulation Unit in Hyderabad as QC Executive from 3rd Jan 2011

till date as below :

Aurobindo Pharma Ltd

Uni-IV, Plot No-4, 34-48, Phase-III,

APIIC,EPIP,Pashamylaram,Medak (DT) Andhra Pradesh

ANVISA,USFDA approved facility.

* Previous Company worked as QC Executive: Since 30 March 2010 to

till 25 Dec 2010 in Formulation Tablet & injection facility as

below:

Torrent Pharmaceuticals Ltd, Indrad.

(WHO Geneva,FDA Uganda,NDA Romania,IDA Netherland,MHRA(U.K),USFDA

(America),TGA (Australia) certified located in Ahmedabad-Mehsana

Highway,

Village: Indrad, Taluka : Kadi, Dist: Mehsana. GUJARAT

* Previous Company worked as a QC Officer: Since 3rd Dec 2007 to 25

march 2010 in Formulation Tablet & injection facility as below :

Macleods Pharmaceuticals Ltd.

(WHO Geneva,FDA Uganda,NDA Romania,IDA Netherland,MHRA(U.K),USFDA

(America) certified located in

Plot No: 25-27, Premier Ind. Estate, kachigam Daman. Pin: 396210

* Previous Company worked as a Production Officer: Since 25 May 2007

to 30 Nov 2007.

Alpha Sanjivani Pharmaceuticals Ltd.

Bhimpore Daman. Pin: 396210

CURRENT JOB PROFILE :

* Responsible for MRR Receiving, Sampling & Analysis allotment of

Packing Material and proper release of material after compliance to

Specification, STP & SOP with advance LIMS,DMS,QMS,TRIMS & ERP

software .

* Initiating PNC, investigation of OOS, Exception, Deviation, Change

Control and regular follow-up till its approval in QMS software.

* Responsible for Training the analyst to perform the testing as per

STP, GTP and SOP with GLP compliance practices.

* Responsible for allotting work to respective analyst and reviewing

the analysis completed documents with respect to the Standard

testing procedure (STP) and Standard operating procedures (SOP)

wherever applicable.

* Responsible for review of Eye drops components, Rubber stopper,Vials & flip off seal & all sorts of Tablet, capsules, Injection

related packing material testing with compliance to world level

regulatory guidelines.

* Responsible for proper submission of all required documents for

regulatory compliance.

* Responsible for preparing Specification & Datasheet, review of

various products.

* Responsible for preparing SOP & reviewing as per due date &

maintaining all document of packing material.

* Verification of Instrument calibration daily & quarterly as per

SOP.

* Responsible for preparing Regulatory COA on letter head as foreign

organization requirement.

* Responsible for preparing & maintaing Specifications & master

specimen card of each product received from PRD respectively.

* Responsible for preparing shade card of carton catch cover, strip &

blister foil.

* Maintaining all the necessary records and registers confirming to

CGMP guidelines.

* Update Transparency of different foreign language with approval of

QC, QA & PRD.

* Coordinate with Head Office and PRD through mail, phone & fax.

* Handled instruments for Finish & RM analysis in Training period.

INSTRUMENT OPERATED

* Atomic Absorption Spectrophotometer (AAS)

* Differential Scanning Calorimeter (DSC)

* FTIR Spectrophometer

* UV Spectrophotometer

* Dissolution & Disintegration apparatus

* Ampoule Snap Tester

* Scuff Proof Tester

* Melt Flow Index Apparatus

* Bursting Strength

* Friability

* Sieve Shaker etc and other all instruments used in regular RM/PM

analysis.

CORE COMPETENCIES:

* Willingness to learn and develop, punctual & progress.

* Positive Attitude and Belief in hard work.

PERSONAL DETAILS :

Name : Vijay.R. Tripathi

Fathers Name : R.S.Tripathi

Date of Birth : 14 Nov' 1984

Gender : Male

Nationality : Indian

Languages Known: English & Hindi, Gujrati.

Passport No. : J4915777

Marital status : Married

Expected Salary : Negotiable

Permanent Add :

Vijay.R. Tripathi

S/O R.S.Tripathi

172, M.L.I.G Barra-5

Near Hanuman Mandir Chauraha.

Kanpur -208027 (U.P)

Corresspondence Address :

Vijay.R. Tripathi

C/O B.Nagaraju

Plot No.316,Sai Bhagwan Colony,

Near Sai Baba Temple,Beeramguda

Medak Dist.,Patancheru Mandal

Hyderabad -502032 (A.P)

DECLARATION:

I here by declare that all the information given by me above is

true to the best of my Knowledge and i hold the responsibility of its

authencity.

Sign:

Date:

(Vijay .R Tripathi)



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