NetSysCon : Mumbai

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  1. Post Count Number #1
    Freelancer
    Join Date
    August 18th, 2010
    Location
    India
    Posts
    16,237

    NetSysCon : Mumbai

    Company Name : NetSysCon

    Company Location : Mumbai

    Company Profile :
    NetSysCon consists of highly qualified professional human resource consultants who have extensive experience of practicing in the field of human resources as line managers. Our advantage is our talent pool, professional commitment and collective knowledge base acquired through intensive training in HR and Quality. This ensures a healthy combination for client organizations in their improvement efforts through one agency

    Services Offered :
    HR Practices
    Reward and Recognition
    End to End Recruitment
    HR Strategy Planning

    Company Address :
    NetSysCon
    G-11, Ground Floor, Suyog Industrial Estate,
    Vikhroli (W), Mumbai 400079

    Website : http://netsyscon.net

    How to submit CV / resume : drsarma@netsyscon.net

    Placement Agencies Mumbai, Manpower Consultants Mumbai, Staffing Companies Mumbai

  2. Post Count Number #2
    IJT addict Guest-IJT's Avatar
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    October 15th, 2010
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    Name : Kumudini Phapale
    Email : kumudini.123.u AT gmail.com
    Designation / Skillset : Regulatory Affairs
    Cover Letter
    To,
    HR,
    Subject : Application for a post of Regulatory Affairs /QA
    Dear Sir,
    I would like to introduce myself as Kumudini Phapale, I wish to apply for a suitable position in Regulatory Affairs based on scientific knowledge, and having knowledge of ICH, CFR GUIDELINES, Documentation in Regulatory Affairs like DMF, CTD, ACTD and Clinical Research. I possess Bachelor of Science (Biotechnology) & basic diploma in clinical research and also did post graduation in drug regulatory affairs (PGDRA). Having 3 months experience as trainee in QA/QC and production at Varun Medico Pvt. Ltd. And 6 months experience in Regulatory as a Trainee in Perfect Pharmaceutical Consultancy Services.
    With utmost respect to values, I promise to serve your organization with integrity, through innovation and by applying thought, day after day. Sincerity, commitment, honesty and best for learning and hard work will be my virtues for the Organization.
    I am attaching my updated CV for your kind perusal.

    Looking forward for your favorable response, thanking you in anticipation

    Thanks and Regards
    Kumudini Phapale

    Resume :
    Objective :
    Seeking to be a part of an internationally recognized progressive organization that offers scope for boosting my knowledge, research and management skills in accordance with the latest trends
    Area of Interest : Drug Regulatory Affairs/QA/QC
    Professional Exposure : Completed 6 months internship at Perfect Pharmaceutical
    Consultancy Services, Pune in Regulatory Affairs.
    Projects Handled : Compilation of QOS, Module 3 as per ICH CTD guidelines.
    Education :
    Course College/University Year Passed
    Advanced Post Graduation Diploma in Drug Regulatory Affairs Global institute of regulatory affairs (GIRA) Institute, Pune 2011
    Basic Diploma Clinical research Management & Regulatory Affairs Haffkine Institute for Training Research & Testing, parel, Mumbai. 2010
    BSc. Biotechnology Mumbai University 2010
    Projects During PGDRA :
    - Project on Common Technical Document (CTD) (quality module) to acquire marketing authorization in ICH countries for Terbinafine Hydrochloride 250 mg Tablet.
    Projects during basic diploma in clinical research and regulatory affairs
    - Project on Committee for Proprietary Medicinal Product (CPMP) to get marketing authorization for TAMIFLU.
    Regulatory Skills :
    - Knowledge of DMF, CTD Module 3 for ANDA and MAA for EU markets through different routes of filing CP, MRP, DCP, National and for US market.
    - Knowledge of Hatch Waxman Act, Schedule Y, Clinical Research.
    - Knowledge about the Requirement of ACTD dossier to get marketing authorization in ASEAN countries.
    - Knowledge about Basic requirements for Dossiers preparation for Marketing Authorisation in Row Market.
    In-plant Training : Completed 2 months inplant training at Varun Medico Pvt. Ltd., at Rabale, New
    Mumbai in Production, QA & QC and was involved in routine activities of
    Production, QA & QC as mentioned below-
    Quality Control/ Quality Assurance :
    A. Hands-on experience of using instruments during training in Quality Control Department : during routine analysis like L.O.D. Analysis, Weight Variation, TLC (Thin Layer chromatography) and Karl Fischer Auto Titrator, UV-Spectrophotometer, IR moisture balance, Polarimeter, Pycnometer, pH meter, Moisture Balance (IR), Melting Point Apparatus, Dissolution Test Apparatus, Disintegration Test Apparatus, Friability Test Apparatus, Leak Test Apparatus..
    B. Maintenance of Quality Control Record in compliance with WHO-GMP and D and C Act, and their Documentation (CoA, MOA, STP, BMR, SOP).
    C. Testing of raw materials, packing materials and finished products (Tablets) as single & multi ingredients as per Pharmacopoeia.
    D. IPQC (In-Process Quality Control) of finished products during manufacturing.
    E. Product Stability Data Preparation.
    Manufacturing and Packing :
    - Manufacturing of different type of oral solid doses form like tablets (coated and uncoated) and powder with the equipment used in Granulation, Compression, Coating, and Packing.
    Conferences and Workshop Attended :
    - BioPharma Institute Programme GMP : Documentation and Record Keeping for Good Manufacturing Practices (An Abridged Course).
    - Conference on IDMA-APA IPC 2010 Thirteenth Pharmaceutical Analysts convention at Hotel Hyatt Regency, Andheri, Mumbai.
    - Workshop on Drug Regulatory Affairs QA/QC by Asian Institute of Health Sciences, Mumbai.
    - Workshop on ICH GCP and pharmacovigilance by Asian Institute of Health Sciences, Mumbai.
    - Workshop on CDM and Medical writing by Asian Institute of Health Sciences, Mumbai.
    - Seminar on Regulatory Affairs by VPM’s Advance Study Centre, Thane.
    Computer Expertise
    - MSCIT in Computers from Govt. Of India
    - Data mining on RA using internet, HTML, XML
    References :
    Mr. Vishweshwar L. Sangmuly Mr. Sanjiv Kumar
    (Director (Technical)) at Regulatory Affairs Manager at
    Perfect Pharmaceutical Consultants Services. Alkems Laboratories Pvt. Ltd.
    -------------------------------------------------------
    More Information about this submission and submitter :-
    ___________________________________________________
    Submission ID : 4212027
    Date & Time : 4th Jun 2011 10:00 PM (UTC)
    IP Address : 120.61.11.48
    Browser Info : Mozilla/5.0 (Windows NT 5.1; rv:2.0.1) Gecko/20100101 Firefox/4.0.1
    Predicted Country : India