Dimple Sutaria MRSC

Senior Quality Assurance Officer at Noumed Life Sciences Limited
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Contact Information
us****@****om
(386) 825-5501
Location
Southampton, United Kingdom, GB

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Experience

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior Quality Assurance Officer
      • Nov 2017 - Present

    • Germany
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • QA Specialist - Task Force Team
      • Mar 2016 - Mar 2017

    • Senior Quality Assurance Officer
      • Sep 2015 - Mar 2016

    • Senior Quality Engineer
      • Jul 2014 - May 2015

      Working in the Supplier Quality Management Team, responsible for Suppliers and Distributors management lifecycle for Medical Devices and Medicinal Products; executing through to approval of Quality Agreements and maintaining the Approved Supplier List.Ensuring compliance with company standards by incorporating 100% of the distributors into the Supplier Management lifecycle and completing 25% of the supplier periodic reviews and.

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior QA Officer
      • Jun 2008 - Dec 2013

      Responsible for the execution, co-ordination and maintaining the GMDP Quality System, ensuring that medicinal products supplied by the company are manufactured and distributed in compliance with the law and the respective Marketing Authorisations. Providing technical and quality support for existing commercial products with from approximately 90 third-party suppliers.

    • QA Officer
      • Aug 2006 - Jun 2008

      Reporting to the Quality Manager, responsible for solely maintaining the key compliance QA systems and undertaking QA activities in key functional areas for the whole company and in doing so supporting Production, QC, Microbiology, Warehouse, Engineering, IT and HR departments on QA related activities.

    • QC Chemist
      • Jun 2005 - Aug 2006

      Performing laboratory procedures and tests including data analysis to the latest Pharmacopoeial methods and in-house test methods for APIs, raw materials and Sterile In-process samples, Finished Product release samples and Stability samples.

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Supervisor/Pharmaceutical Scientist
      • Nov 2003 - May 2005

      Responsible for the management of daily operations and activities of the laboratory and acted as direct source of feedback to the Senior Management Team. Developed formulations and analysed them using techniques such as HPLC, UV spectrometry, Centrifugation, Rheology and Franz cells (in vitro technique)

    • Oligonucleotide Technician
      • Jul 2003 - Nov 2003

      An analytical role focusing on detailed study and characterization of Oligonucleotides.

    • Production Technologist
      • Sep 2001 - Jul 2003

      Working to GMP, ISO9001 and other regulatory standards for a Pharmaceutical Production Area. Responsible for Reagent and media preparation and sterilisation, specialised equipment assembly and sterilisation, environmental monitoring and maintaining cleanroom standards.

    • United Kingdom
    • Retail
    • 700 & Above Employee
    • Optical Assistant
      • 1992 - 1999

      A large number of responsibilities including liasing with customers, repairing spectacles, training customers on aspects of contact lens use and general reception duties.

    • Post Office Counter Assistant
      • 1994 - 1994

      1994-2008 Responsible for over the counter activities involving customer focus, promoting new products and weekly stock balancing and accounting

Education

  • University of Leeds
    Certificate in Clinical Research
    2002 - 2003
  • University of Portsmouth
    BSc (Hons) Pharmacology
    1996 - 2000
  • Totton College
    'A' Levels in Biology, Chemistry and Maths & Mechanics
    1993 - 1996

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