Shveta Mehta

HSEQ Manager, ANZ at IMCD Australia Ltd
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Melbourne Area
Languages
  • Hindi -
  • Punjabi -

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Credentials

  • Leadership Training
    Catalent Pharma Solutions
    May, 2014
    - Oct, 2024
  • Introduction to Regulatory Affairs in Australia
    ARCS Australia Ltd
    Feb, 2014
    - Oct, 2024
  • Kaizen Training
    Kaizen
    Feb, 2009
    - Oct, 2024

Experience

  • IMCD Australia Ltd
    • Chemical Manufacturing
    • 1 - 100 Employee
    • HSEQ Manager, ANZ
      • Apr 2022 - Present

  • Max Biocare
    • Australia
    • Wellness and Fitness Services
    • 1 - 100 Employee
    • Head Of Regulatory Affairs
      • Nov 2016 - Present

    • Regulatory Affairs Manager
      • Nov 2014 - Nov 2016

  • Catalent Pharma Solutions
    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Quality and Regulatory Affairs Associate
      • Dec 2012 - Nov 2014

      - Listing and registering products - Checking the art work - Provide regulatory input to product lifecycle planning - Evaluate regulatory impact on proposed products - Dossier preparation and gap analysis for dossier submitted to customers for listing or registration purposes - Applying and maintain different licenses - Maintain relationships with customers and suppliers - Responding to customer queries for Quality and regulatory requirements on daily basis - Preparing SOPs and Work instructions and training of relevant staff. - Updating and maintaining Product specifications - Conducting Product Quality reviews, preparing PQR/APR reports and follow ups - Conducting Raw Material Evaluation (RME), thorough knowledge of RME process - Preparing New Raw material specifications as per monographs and internal standards - Maintaining and updating RM specifications

    • Team Leader – Quality Department
      • Jun 2008 - Mar 2010

      - Lead a team of nine analysts to adhere to daily business requirements of production environment. - During this time she also developed new processes to get efficient results via parallel testing techniques. This led to completion of results before time thus achieving Service Level Agreements.- Prepared the lab for external audit and conducted internal audits. This helped to ensure that company is working under prescribed regulations.- Participated and contributed in the company Kaizen process. - Encouraging strong team work within the team, leading to high efficiency with personnel and customer satisfaction - Liaising with warehouse, Planning and purchasing department on regular basis- Regular contact with suppliers and customers (internal and external)- Training of new staff, development of staff on regular basis (cross training)- Directly reporting to QC manager- Handling everyday issues in the team and within the laboratory, contributing to overall management of the lab- Coordinating multiple projects, completing projects well within given timeline- Yearly and half yearly reviews of team- Gaining deep knowledge of raw materials, herbals, their maintenance and best methods of testing’s as per BP, USP and BHP- Writing and controlling SOPs, regular updating and maintaining- Purchasing and looking after the maintenance of Instruments

    • Analytical Scientist
      • Jan 2006 - Jun 2008

  • Mayne Pharma
    • Australia
    • Pharmaceutical Manufacturing
    • 400 - 500 Employee
    • Analytical Scientist
      • Nov 2004 - Aug 2005

Education

  • Punjab Agricultural University
    Master's Degree, Microbiology, General
    1997 - 1999
  • Panjab University
    Bachelor's Degree, Chemistry and Biology
    1994 - 1997

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