Proalgen Biotech Ltd Chennai : Executive Formulation

[Rajkumargautam]

Proalgen Biotech Ltd. Chennai : Executive-Formulation & QA

Website: http:// www.proalgenbiotech.com

Keywords: Formulation Executive


Designation: Executive-Formulation & QA
Experience: 3 - 7 Years
Location: Chennai
Compensation:
Rupees 50,000 - 2,25,000
Education:
UG - B.Pharma - Pharmacy
PG - M.Pharma - Pharmacy
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Healthcare, Medical, R&D
Posted Date: 27 Apr

Job Description:
Exposure in good pharma industry specific. Formulation and Quality Assurance

Desired Candidate Profile:
Experience in good pharma Company-3 years

Company Profile:
We are a leading biotech house working pan India and catering neutraceuticals /pharmaceuticals/ cosmoceuticals. Currently we have an opening based in Chennai.

Address: Not Mentioned

Email Address: formulation.biomax@gmail.com

Telephone: 044-42919400

Reference ID:
Exec/PBL/Chn/Form

Keywords: Formulation Executive

[Guest]

RESUME
SAGADEVAN.M
Mail Id : Sagadevan79 AT yahoo.co.in
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OBJECTIVE :
Seeking a challenging assignment to utilize my professional skills in the area of quality control laboratory to build a motivated and skilled workforce and they’re by upholding the name of the organization.
WORK EXPERIENCE :
- Currently employing as an QA-Executive in SGS india Pvt. Ltd., Chennai. since Oct 2009 to till date.
- Worked as a QC- Executive in Pharmazell india Pvt. Ltd., Chennai. since Sep 2008 to Oct2009.
- Worked as a Analytical Development Executive in Micro Labs Pvt. Ltd., Hosur, since May 2005 to sep 2008.
- Worked as a QC- Analytical chemist in Avon Organics Pvt Ltd.Solapur Maharastra, India, since August 2002 to May 2005.

Job Responsibilities :
- Having thorough knowledge in complete Review of Analytical method validation, reports for Raw materials, Intermediates, Finished products, Stability samples, calibration documents and Analyst Qualifications.
- Provide leadership to staff in the form of motivating, training and technical assistance.
- Having experience in handling of QMS documents like Deviations, OOS, CAPA, OOT and Change control.
- Investigation of Customer’s Complaints.
- National/International Customer’s Audits faced during the career like,WHO and USFDA.
- Having Experience in Methods, Facilities and Equipment.
- Organizing and follow-up internal audits and reviews.
- Having Experience in Pharmaceutical products and analysis of different types of Raw materials, Syrups, Tablets, capsules and liquid oral formulations.
- Having experience and capabilities to undertake Instrumentation and Calibration of HPLC, GC, UV, Dissolution apparatus, FTIR.
- Stability studies of drugs at real time and accelerated conditions

- Preparation of analytical procedure for analysis.
- Preparation of SOP’s for instruments.
- COA Authorization for Test Reports.
SOPHISTICATED INSTRUMENTS HANDLING :
Instrumental Exposure :
HPLC :
SHIMADZU LC 10 ATVP, SHIMADZU LC2010AHT, AGILENT 1100, WATERS 2695
SOFTWARE :
CLASS –VP, CHROMELEON, EMPOWER, MILLINIUM, LC SOLUTION
SPECTROPHOTOMETER :
FTIR-8300 SHIMADZU, UV-160A SHIMADZU
DISSOLUTION APPARATUS :
Electrolab –TDTO8L
GAS CHROMATOGRAPHY :
Perkin Elmer-Clarus 500
EDUCATIONAL QUALIFICATION
EXAMINATION YEAR OF PASSING BOARD/UNIVERSITY PERCENTAGE
S.S.L.C 1994 Govt.High School, Melmoil. 77.5 %
HSC 1996 National High Sec .School, Gudiyatham. 75.6 %
B.Sc (Chemistry) 1999 University of Madras 63.4%
M.Sc (Chemistry) 2002 University of Madras 57.2%

[Guest]

VIJAYAKUMAR.M
mvk226 AT gmail.com
SUMMARY OF QUALIFICATIONS
Over 9 years of experience in Pharma industry with good Analytical skill and problem
solving ability and capable of meeting deadlines in Pharma industry.
- Proven skills as a good team leader, developing and motivating teams to achieve their
targets.
Professional communication skills include fluency in English, kannadam, Tamil.
- Knowledge of principles and operations of all major analytical instruments and
equipments such as HPLC, Gas chromatographs, Spectrophotometers (UV/IR), Polari
meter, Titrators, stability chambers etc.
- Knowledge of Analytical method development and validation.
- Total QC/QA activities including stability, QA/QC documentation, review, Release &
developmental quality assurance etc.
PROFESSIONAL EXPERIENCE
Current Employment
: Biocon Limited, Bangalore (From may-2006 to till date)
Designation
: Sr. Executive Quality control
Previous Employment- 2 : Shasun Chemicals & Drugs Ltd., Pondicherry.
An ISO 9001 :2000 & USFDA accredited company.
Designation
: Officer - Quality Control. From May 2003 to April 2006.
Previous Employment- 1 : Shasun Research & Development centre, Velacherry, Chennai
Designation : Management Trainee
From Dec 2001 to April 2003.

Key area responsibilities (KRA) :
- Completely Taking care of Analytical method validation team and actively
Participating in Analytical and Cleaning Method Validation according to ICH
guidelines and ensuring lab compliance as well regulatory requirements and also timely
completing the projects with online documentation.
Planning and execution of complete validation team functions.
Preparation Protocols, Observation data sheet & reports, review and execution of
quality control procedures,
Planning & execution of Analytical Method transfers to
inter-lab as well customers.
Ensuring compliance as per cGMP/GLP requirements
Analytical support to process validations.
Preparation of calibration schedule weekly, monthly and yearly.
As per the schedule executed the calibration for analytical instruments.
Working in close coordination in work groups for conducting process audits and d
detailing on quality requirements and finalizing the quality plan.
Worked as a group leader for Intermediates and finished products.
Planning and executing various analytical methods, Pharmaceutical
Development System and New Drugs and Intermediates.
Responsible for all group leader activities related to analysis, Review,
Documentation & approval for all intermediates and finished products.
Work allotment, laboratory investigations/ deviations/incident & OOS etc.
Responsible for 21CFR part 11 compliance.
Planning of analysis on daily, monthly and yearly basis, according to our
Production and marketing plan.
Making COA as per the customer requirements.
Review and approval of laboratory results and documentation.
Analytical support to process validations.
Preparation of calibration schedule weekly, monthly and yearly.
As per the schedule executed the calibration for analytical instruments.
Working in close coordination in work groups for conducting process audits and
Detailing on quality requirements and finalizing the quality plan.
INSTRUMENTS HANDLED
HPLC - Agilent , Waters & SHIMADZU
GC - Agilent ; SHIMADZU 17A, GC2010 ; Perkin Elmer Gc
FTIR -Perkin Elmer 1600 Series ; Thermo Nicolet FTIR 5700
UV – Vis Spectrophotometer (UV240PC) Shimadzu – Japan.
Polarimeter – Autopol Riv Automatic and Ruddloph advanced instrument.
Particle Size analyzer-Malvern Master sizer (Hydro 2000S)
EDUCATION
M.Sc., Chemistry (First class)
A.V.V.M Sri Pushpam College,
Poondi, Thanjavur (Dt),
Affiliated to Bharathidhasan University Trichirapalli.
B.Sc., Chemistry (First class)
T.U.K. Arts College,
Thanjavur (Dt)
Affiliated to Bharathidhasan University, Trichirapalli.