www.cppri.org.in Recruitment 2012 Central Pulp and Paper Research Institute : Scientific Assistant

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  1. Post Count Number #1
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    www.cppri.org.in Recruitment 2012 Central Pulp and Paper Research Institute : Scientific Assistant

    Name of the organisation : Central Pulp and Paper Research Institute (cppri.org.in)
    Name of the post : Recruitment for Scientific Assistant in 2012

    Advertisement for the post of Senior Scientific Assistant published in Employment News, dated 31st Dec.2011 -6 January 2012

    Advertisement for the post of Senior Scientific Assistant in the pay scale of 9300-34800+4200 (GP)

    Post : Senior Scientific Assistant

    Number of Post : 1 (One)

    Scale of Pay : 9300 -34800 + GP 4200

    http://www.cppri.org.in/job-openings.html
    http://www.cppri.org.in/gifs/SSA.doc

    Essential Qualification : M.Sc.(Chemistry) or B.E./B.Tech. (Pulp & Paper/Chemical Engineering/Pulp & Paper Engineering) or recognized equivalent qualifications with minimum 60% marks

    Age limit : 28 years

    GENERAL CONDITIONS :
    1. The prescribed qualification should have been obtained from recognized University/ Institutions.
    2. The post carries usual allowances i.e. D.A., H.R.A., Transport allowance as per Central Government rules and benefits like Contributory Provident Fund, Group Saving Linked Insurance, Medical as per Institute rules.
    3. The retirement age is 60 years.
    4. The crucial date for determining the upper age limits, qualifications, and/or experience shall be the closing date of receipt of applications.
    5. Age limit is relaxable as per Govt. rules issued from time to time for SC/ST/OBC/PH and other categories. Persons suffering from not less than 40% of the relevant disabilities shall alone be eligible for benefit for the relaxation.
    6. Photocopy of the Caste/Tribe and physical handicapped certificate issued by competent authority is required to be attached.
    7. Application duly completed in all respect should be submitted to
    Director,
    Central Pulp and Paper Research Institute,
    Post Box No. 174,
    Saharanpur-247001 (U.P.)

    within 30 days of publication of the advertisement together with Demand Draft of Rs. 100/- non-refundable with the validity of six months drawn in favour of Central Pulp And Paper Research Institute, payable at Saharanpur. (No demand draft is required from SC/ST, Physically Handicapped an female candidates and from departmental candidates, if any).
    Attached Files Attached Files
    Last edited by mariammal; January 12th, 2012 at 11:58 AM.

  2. Post Count Number #2
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    Name : Vipul joshi
    Email : vipuljoshi7 AT yahoo.com
    Designation / Skillset : QC Manager
    Dear Sir,
    Iam vipul joshi, working as mangar-QC in one of the reputated pharmaceutical formulation company in Dehradun. I am also looking QA activities for last one year. I have around 15 years experience & worked in maharashtra, Gujarat & mumbai with big groups like glaxosmithkline, aventis phama etc.
    I am very keen to relocate in maharashtra & mumbai. Hoping to receive your positive response for equivalent position in QC / QA. Please find attached herewith my CV for your kind consideration.
    Thanks & regards
    vipul joshi

    Resume :
    OBJECTIVE :
    Fifteen years of versatile experience in quality control department of Indian & Multinational pharmaceutical organizations and exposure to QA activities that
    can make full use of my skills and abilities.
    EDUCATIONAL QUALIFICATION :
    M.Sc. ( Organic Chemistry ) with First division from University of Garhwal, Uttarakhand in 1994.
    B.Sc. ( Chemistry, Botany ) with First division from University of Garhwal, Uttarakhand in 1991.
    12th & 10th with First division in the year 1988 & 1986 respectively.
    ADDITIONAL QUALIFICATION :
    Computer Diploma in Office Automation.
    FDA APPROVAL :
    FDA approval in Chemical and Instrumentation from FDA Maharashtra.
    EXPERIENCE :
    1.Uni Medicolabs, Dehradun
    ( Associated with Unichem Laboratories Ltd. )
    Duration : June 2010 to till date
    - Working as Manager-Quality Control ( Also Managing QA from Aug.2010 )

    2. Hema Laboratories Pvt. Ltd., Dehradun
    Duration : Jan. 2010 to June 2010 ( 6 Months )
    - Worked as Manager-Quality Control
    3.Raptakos, Brett & Co. Ltd., Thane
    Duration : From Oct. 2007 to Sep. 2009 ( 2 Years )
    - Worked as Manager -QC & pkg.
    4. Aventis Pharma Ltd., Ankleshwar
    Duration : From Sep. 2006 to Oct. 2007 ( 1 Year )
    - Worked as Quality Control Executive
    5. GlaxoSmithkline (GSK) Pharmaceuticals Ltd., Nashik
    Duration : April 1998 to Aug. 2006 (More than 8 Years )
    - Worked as Skilled Staff ( Quality Control Chemist) in Q. C. Department
    6. Frontline Pharmaceuticals Pvt. Limited, Vasai, Thane
    Duration : Feb. 1997 to April 1998 ( 1 Year )
    -Worked as Quality Control Chemist
    7. Bassin Drugs Limited , Vasai, Thane
    Duration : Aug. 1995 to Feb. 1997 ( 11/2 Years )
    -Worked as Quality Control Chemist
    Expertise :
    Technical :
    1. Proficient with sophisticated instruments like GC, HPLC, IR, NIR, UV etc.
    2. Calibration of various laboratory equipments like GC, HPLC, IR, UV etc.
    3. Trouble shooting for most of the sophisticated instruments.
    4. Knowledge of testing of Raw Materials, Packaging Materials, Finished Products ( Liquids, Tablets, Capsules, Injectables, Ointments & Creams ).
    5. Analytical method validation for different products.
    6. Knowledge of Regulatory requirement and drug rules.
    7. Well conversant with Stability studies & date expiry samples.
    8. Knowledge of MSA study ( Measurement System Analysis ), pertaining to validation with six sigma tools.
    9. Involved in extensive analysis during new product launching.
    10. Exposed to Microbiological Section including Antibiotic assay, Sterility, Pyrogens etc.
    11. Inprocess GMP rounds in Production area.
    12. Art-Work preparation for all packaging materials of Local & export products.
    13. Faced WHO-GMP audit & also exposed to EU-GMP.
    14. Preparation of process validation protocol.
    15. Handling of change control & deviation.
    Managerial :
    1. Responsible for planning the work so that material can release at the earliest to Production / Packing / Sale.
    2. Approval or rejection of Raw Materials, Packaging Materials, Intermediates, Bulk & Finished Products.
    3. Responsible for preparation of SOPs / PQS /ATR.
    4. Handling of failure / deviation & OOS / OOT results.
    5. Handling of Market complaints.
    6. Vendor audit- Exposed to big suppliers like Hindalco, PG Foils etc.
    7. To review & check the BMR / BPR for its compliance as per requirement.
    8. Arrange & coordinates meetings with Managers/ Staff.
    9. Documents-Verification & Approval.
    10. Approval of master checklist for audits, trainings & delivering seminars.
    Seminar Attended :
    Attended seminar on HPLC method validation & trouble shooting organized by IDMA in Mumbai.

    -------------------------------------------------------
    More Information about this submission and submitter :-
    ___________________________________________________
    Submission ID : 4440087
    Date & Time : 3rd Aug 2011 10:40 AM (UTC)
    IP Address : 117.241.219.229
    Browser Info : Mozilla/4.0 (compatible; MSIE 8.0; Windows NT 5.1; Trident/4.0; InfoPath.2; .NET CLR 1.1.4322)
    Predicted Country : India

  3. Post Count Number #3
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    LOOKING FOR A JOB

    IS DER ANY VACANCY FOR RETIRED NAVY PERSON HAVING EXP OF 28 YEARS IN AVIATION BRANCH.. INTERESTED IN FIRE FIGHTING OFFICER AND SECURITY OFFICER

    There is no vacancy for retired navy person in this recruitment to keep a watch on the official website.
    Last edited by Answer; February 28th, 2012 at 12:45 PM.