www.ipft.gov.in Recruitment 2011 Institute of Pesticide Formulation Technology : Analytical Scientist, Technical Officer

[muthukalee]

INSTITUTE OF PESTICIDE FORMULATION TECHNOLOGY (IPFT)
(An Autonomous Institution of Ministry of Chemicals & Fertilizers,
Department of Chemicals & Petrochemicals, Govt. of India)

1. Technical Officer [Pay Band Rs. 15,600-39,100 with GP of Rs. 5,400.00]
No. of Posts : 01
Essential Qualifications & Experience : B.Sc. in Chemical Engineering / B.Tech. with 6 years experience in Central / State Govt. / PSUs / Universities / Research Institute of Repute / Laboratories / Reputed Private Companies.
OR
Ph.D. in Engineering.

2. Scientist (Analytical) [Pay Band Rs. 9,300-34,800 with GP of Rs. 4,200.00]
No. of Posts : 01
Essential Qualifications & Experience : B.Sc. with 65% marks & minimum 2 years experience in Central / State Govt. / PSUs / Universities / Research Institute of Repute / Laboratories / Reputed Private Companies.
OR
Master Degree in Organic / Analytical / Agricultural Chemistry with not less than 55% marks.

3. Scientist (OPCW) [Pay Band Rs. 9,300-34,800 with GP of Rs. 4,200.00]
No. of Posts : 01
Essential Qualifications & Experience : B.Sc. with 65% marks & minimum 2 years experience in Central / State Govt. / PSUs / Universities / Research Institute of Repute / Laboratories / Reputed Private Companies.
OR
Master Degree in Organic / Analytical / Agricultural Chemistry with not less than 55% marks.

4. Scientist (Pilot Plant) [Pay Band Rs. 9,300-34,800 with GP of Rs. 4,200.00]
No. of Posts : 01
Essential Qualifications & Experience : B.Sc. in Physics, Maths & Chemistry with minimum 65% marks and 2 years experience in the field.
OR
Three years Diploma in Engineering with 3 years experience.

5. Scientist (Biosciences) [Pay Band Rs. 9,300-34,800 with GP of Rs. 4,200.00]
No. of Posts : 02
Essential Qualifications & Experience : B.Sc. with 65% marks & minimum 2 years experience in the field.
OR
Master Degree in Plant Pathology / Agriculture / Entomology / Agronomy with not less than 55% marks.

HOW TO APPLY :
Interested candidates may download application form from our website www.ipft.gov.in and send duly filled application in the prescribed format, super-scribing the name of the post applied for, along with a Non refundable fee of Rs. 300.00 (For General & OBC) by Demand Draft from any Nationalized Bank favoring “Institute of Pesticide Formulation Technology, Gurgaon” payable at Gurgaon so as to reach the office of the Director indicated below within 30 days from the date of publication of the advertisement. SC/ST and Physically Handicapped candidates are not required to submit the application fee.

The complete application along with recent passport-size photograph and copies of relevant certificates and other testimonials in support of age, qualification, caste & experience etc. should be sent in a closed cover super scribing.

“Application for Technical/Scientific Position for the post S. No. [ ] of “___________”

To,
The Director
Institute of Pesticide Formulation Technology (IPFT)
(An Autonomous Institution of Ministry of Chemicals & Fertilizers,
Department of Chemicals & Petrochemicals, Govt. of India)
Sector-20, Udyog Vihar, Opposite Ambience Mall, NH-8,
Gurgaon – 122 016 (Haryana)

So as to reach within 30 days from the publication of the advertisement.

More Details : http://www.ipft.gov.in/career1.htm

[Guest-IJT]

Name : sachin
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Email : sachinrana11@rediffmail.com
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Designation / Skillset : sr research scientist
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SACHIN RANA
________________________________________

Dear Sir


This is in reference to the advertisement I am writing to express my interest in joining your team as a SR RESEARCH SCIENTIST.
My resume is enclosed for your review and consideration. To describe myself in a nutshell, I am hardworking; ready to take up any challenge of life abreast with the latest trends and a team player with excellent communication skills.

My basic objective is to hone in my skills for comprehensive personality development and be an epitome of trust and reliability in the corporate world. My prime goal is to understand professional environment and capitalize on opportunities.

Professionally I am looking for an opportunity that will help me utilizing my skills in the above areas. My detailed resume is enclosed herewith for your kind perusal and consideration.

I am confident that you would find my strong initiatives and commitments to excellence coupled with demonstrated experience and exposure ideal for the position.
I would welcome a personal meeting to further discuss your requirements and my ability to meet the same.

Thanking you for your consideration and forthcoming response.

Yours Sincerely

Sachin Rana

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Resume :
SACHIN RANA

________________________________________
RESEARCH SCIENTIST - CLINICAL PHARMACOLOGY & PHARMACOKINETICS

• Technically astute, diligent & passionate professional with an experience of over 6 years in the field of Bioanalytics using HPLC and LCMS/MS in Bioequivalence and Bioavailability studies, currently spearheading with Ranbaxy Research Laboratories as Sr. Research Scientist - Clinical Pharmacology and Parmacokinetics.
• Keep abreast with the new technologies in this field. Expertise in developing products with effective and modernized tools and equipments while managing the inventory in the company. Successfully performed several Bioanalytical Studies for submitting to various regulatory agencies like CPMP, USFDA, Brazil.
• Knowledge of GLP and GCP techniques. Expertise in developing and validating bioanalytical methods as per FDA guidelines and Brazilian resolution for validation.
• Ability to conceptualize the processing for the product development with careful & sophisticated quality control measures in compliance to the specified standards while performing root-cause analysis to prevent any reoccurrences & defective issues.
• Participate in protocol development, Sop training, Trouble shooting of LCMS\MS for review of QA procedures, Audit Plans and checklists Monitoring of clinic (e.g stability related issues for some moleculesetc.)
• Ability to use sound decision-making skills and effectively perform in a self-directed work environment.
• Demonstrated ability to manage human, financial and material resources towards the achievement of stated objectives, to plan and manage work programs and to lead, motivate and provide effective guidance to a team of professional and support staff.
________________________________________
CAREER HIGHLIGHTS

RANBAXY RESEARCH LABS Since Mar 2005
Sr. Research Scientist - Clinical Pharmacology and Parmacokinetics

• Responsible for the Method development and validation for Finasteride, Atorvastatin, Acyclovir, Omeprazole, Ramipril.
• Work on BA (Bioavailability)\BE (Bioequivalence) Studies which is an important part of clinical research. Conduct BE studies for Itraconazole, Divalproex, Loratadine, Psedoehedrine & fexofenadine, Ramipril, Acyclovir, Felodipine, Perindopril, Mycophenolic acid. Process clinical samples of both test and reference drug and then analyze them on LCMS\MS.
• Maintained Database for drugs under following categories - Antimanic, Antihypertensive, Antipsychotic, Antibiotics, NSAIDS, Antianxiety, Anticonvulsant. Prepare database for over 150 drugs targeted for ANDA submission.
• Determine Biological matrix using LCMS/MS following GLP techniques.
• Ensure that Documentation are done as per the departmental standard operating procedures (SOPs) & regulatory guidelines. Manage the printing of all the analytical data including chromatograms in Nugenesis (a central data base).
• Identify the advancements in the field of clinical pharmacology and pharmacokinetics
• Carry out BA-BE (Bio availability- Bio equivalence) studies. Provide support to the various PDTs.
• Prepare synaptic protocol and submit it to CROs (Clinical Research Organization).
• Review the Draft protocols and send it back to CROs with modifications, if any.
• Get IRB approval for the new product. Get BENOC (Bioequivalence No Objection Certificate) from DCGA.
• Conduct statistical and pharmacokinetic analysis of the pilot study report. Respond timely and adequately to FDA deficiencies and prepare justification reports. Review reports of pivotal tests and submit them to RA.
• Part of the BAT to discuss the development of the new product and approve/reject it for further studies.
• Gather useful information on drug molecule by reviewing research articles and review articles; information on Internal Standard to be used for the drug molecule by reviewing various sites on internet.
• Work under the GLP environment as per the prescribed procedures defined in SOP’s (Method SOP, General SOP, and Laboratory SOP) and Protocol. Research literature on various useful sites which give important information about the drug before and during Method Development is the key part of my job.
• Perform all Exercises of Method Validation. Write Method SOPs.

SUNPHARMA ADVANCED RESEARCH CENTER (SPARC) Dec 2004 – Mar 2005
Research Assistant, Analytical Division

• Conducted Analytical testing of finished products for ANDA submission using HPLC, Dissolution techniques.

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EDUCATIONAL CREDENTIALS

Masters of Pharmacy in Quality Assurance 2004
Faculty of Pharmacy, Hamdard University, New Delhi

Bachelors in Pharmacy 2002
Hamdard University

Diploma in Pharmacy 1998
PUSA

Computer Proficiency
Office Automation, Internet Applications

Trainings Attended
• Liquid Handling system at Ranbaxy R&D.
• “Columns used in LCMS/MS and Extraction Techniques” at Le Meridian conducted by waters.
• Communication skills, Motivation, Leadership qualities, Team building and Time Management.

Academic Accolades
Qualified GATE in 2002

Languages Known : English, Hindi, i
References : Available on Request



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More Information about this submission and submitter :-
___________________________________________________

Submission ID : 4211548
Date & Time : 4th Jun 2011 5:51 PM (UTC)
IP Address : 14.98.87.114
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