Ajmil Enterprises : Mumbai
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  1. March 2nd, 2011, 01:14 PM Post Count Number #1
    muthukalee
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    August 18th, 2010
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    Ajmil Enterprises : Mumbai

    Company Name : Ajmil Enterprises

    Company Location : Mumbai

    Company Profile :
    We are one of the leaders in Manpower recruitment consultancy in India, we have associated offices are in Delhi, Bangalore, Cochin and Trivandrum. We are highly equipped and undergone an intense STUDY, SURVEY and ANALYSIS of all categories of Manpower in India. Because of this professional dedication, we are well established in recruitment of personnel in variety of INDUSTRIES and other SERVICE ORIENTED JOBS

    Services Offered :
    Advertisement
    Requirement Programme
    Data Bank
    Foreign Employer's Duty

    Company Address :
    Ajmil Enterprises
    21, Dr. V. B. Gandhi Marg,
    Opp. Forbes, Fort, Mumbai - 400001.

    Website : http://www.ajmilenterprises.com

    How to submit CV / resume : ajmilenterprises@gmail.com

    Placement Agencies Mumbai, Manpower Consultants Mumbai, Staffing Companies Mumbai
  2. June 4th, 2011, 11:54 AM Post Count Number #2
    Guest-IJT
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    Name : Narayni Jay. Kate
    Email : narayani_jay AT rediffmail.com
    Designation / Skillset : Regulatory Affair Executive
    Dear HR,
    Here I am Enclosing my C.V. Currently I am working with Mihika Pharmaceuticals as an Regulatory Affair Executive,
    located at Mulund (Mumbai), I am Staying in Airoli, Navi mumbai, INDIA.
    Thanks & Regards
    Mrs. Narayni Jay Kate

    Resume :
    Summary
    Graduate of a Pharmacy with 5.7 years of experience out of which 1.6 years in Quality Assurance and 1.7 years in regulatory affairs and 2.4 years of experience in pharmacy practice. Expertise includes documentation in Quality Assurance and preparation of dossiers in Regulatory Affair.
    Employment
    Currently working with :
    - Organisation : Mihika Pharmaceuticals, Mulund (Mumbai).
    Designation : Regulatory Affair Executive.
    Duration : From 3rd March, 2011-till date.
    Job Profile involves –
    1. Prepare documents required to apply WHO GMP certificate, Applied for COPP certificate
    2. Prepared ACTD dossier for Cameroon, Sierra Leone, Nigeria, ect.
    - Organisation : Kilitch Drugs India Ltd., Rabale (Navi Mumbai).
    Designation : RA Officer.
    Duration : From 17th May 2010-03rd March 2011
    Job Profile involves –
    1. Preparation of dossiers for registration of Pharmaceuticals products for Russia, Ukraine, Mosambique, Oman, Chile, Panama, GCC, Philippines, Kenya, Paraguay, Nigeria, Nepal, Mali, Sierra Leone etc.
    2. Sample preparation for registration in various countries.
    3. Checking of Artwork for above mention countries.
    4. Replying queries for Unichem, Lupin, Oman.
    Previous Employment :
    - Organisation : SVS MEDICO located at Chembur, Mumbai
    Designation : Pharmacist.
    Duration : From 15th January 2008 – 15th May 2010.
    - Organisation : CIPLA located at Vikroli, Mumbai.
    Department : Product Registration Cell
    Designation : Trainee.
    Duration : From 21st May 2007 – 26th October 2007.
    Job Profile involves -
    1. Preparation of dossiers for registration of Pharmaceuticals products for Kenya, Hongkong, Mauritius.
    2. Replying queries received from above mention countries.
    3. Checking of Artwork for above mention countries.
    4. Preparation of dossiers for Tenders purpose for Burkina Faso, Kenya, Hongkong, Mauritius, Burundi.
    - Organisation : BDH Industries Ltd. located at Kandivali, Mumbai.
    Department : Quality Assurance
    Designation : Junior Chemist
    Duration : From 3rd November 2005 – 18th May 2007.
    Job Profile involves -
    1. Preparation of documents as required by the WHO-GMP such as Standard Operating Procedures relating to various aspects of Production activity.
    2. Documentation of Master Validation Programme, Master Calibration Programme, Annual Product review & Retrospective validation, Process validation.
    3. Updating of Specifications of Raw materials, Bulk and Finished Products for various Dosage forms.
    4. Monitoring Stability studies data.
    5. Perform IPQC Test for various Dosage forms.
    6. Prepare Q.A. Calender, Site Master File.
    7. Keep records for Destruction of dosage form, labels, cartons, literature, aluminium foil, container of various products, etc.
    8. Log Book check for Tablets, Bond, External Liquid, Raw material store room, Ointment, Capsule and Injection Department.
    9. Temperature mapping.
    Other Activities : Attended GMP training Programme.
    Education
    Bachelor of Pharmacy (1st Class), March 2005
    SNDT Women’s University of Mumbai, C. U. Shah College of Pharmacy.
    Academic
    - Industrial Training
    Organisation : FRANCO-INDIAN PHARMACEUTICALS PVT. LTD. Located at Andheri, Mumbai.
    Designation : Trainee.
    Duration : One month.
    - Projection & Seminar on
    Semecarpus Anacardium – A Drug Profile
    Guide – Dr. Mrs. Nirmala Grampurohit.
    -------------------------------------------------------
    More Information about this submission and submitter:-
    ___________________________________________________
    Submission ID : 4207536
    Date & Time : 3rd Jun 2011 2:00 PM (UTC)
    IP Address : 113.193.65.56
    Browser Info : Mozilla/5.0 (Windows NT 5.1; rv:2.0.1) Gecko/20100101 Firefox/4.0.1
    Predicted Country : India