Andy Gibson

Head of Manufacture and Supply at SiSaf Ltd
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United Kingdom, UK

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Satish Kumar V

Andy Gibson is a goal oriented professional and his extensive experience in Quality speaks for itself in terms of his excellence at work. He was a Project Quality head for a 100M GBP greenfield project in Bengaluru. Andy was involved in developing and implementing a comprehensive validation and qualification strategy for all utilities, equipments and processes and ensured compliance as per GSK requirements. One thing that sets Andy apart from his peers is his willingness to put in more than his 100% to be able to capitalise on an opportunity when it shows itself. Apart from being a good person, Andy is a great leader and mentored many people during his tenure. I had a wonderful time working with him in GSK Vemgal project for a period of 3 years. His extensive experience will be a great asset to any organization he chooses to work for.

Pooja Grover

I had the pleasure of working with Andy for about four years at GlaxoSmithKline for a factory project. His skills and expertise in Pharmaceutical Project Management are exceptional (I have learnt a lot from him!). He has excellent domain knowledge. Andy is a stickler for time management with an eye for details. He encourages problem solving through team engagement. He is also a great coach and mentor, always empowering, inspiring and looking out for his team. Andy would be an invaluable asset to any role or assignment he decides to take up.

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Credentials

  • Fellow Chartered Chemist of the Royal Society of Chemistry
    Royal Society of Chemistry
    Mar, 2021
    - Sep, 2024
  • Chartered Chemist (CChem)
    Royal Society of Chemistry
  • Fellow of Royal Society of Chemistry (FRSC)
    Royal Society of Chemistry

Experience

    • United Kingdom
    • Biotechnology Research
    • 1 - 100 Employee
    • Head of Manufacture and Supply
      • Jan 2020 - Present
    • IT Services and IT Consulting
    • 1 - 100 Employee
    • Director Of Quality
      • Sep 2019 - Dec 2019

      Having left GSK after completing a Global Assignment, I am now seeking a new role. Having left GSK after completing a Global Assignment, I am now seeking a new role.

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Product Quality Leader
      • Dec 2018 - Sep 2019

      Supporting product transfers to North African and Gulf markets to deliver localised manufacturing strategies.

    • Project Quality Lead
      • Jun 2015 - Nov 2018

      A global assignment providing Quality leadership to a 100M GBP greenfield factory project in Bengaluru (India). Major achievement include; • Selection and on-boarded Quality team (25 FTE) into project roles with clear transition path into operation roles post start-up. • Implementation of lean and effective site Quality Management System focused on ensuring clear and simple instructions were provided at operational level. • Championing use of Quality Risk Management techniques and coaching of team to ensure Right First Time product transfers were achieved. • Developing and implementing a comprehensive validation / qualification strategy for all utilities, equipment and processes that ensured compliance and supported project timelines and requirements. • Creating and delivering a Data Integrity plan with major focus on communication and education to ensure a sustainable data integrity culture was established. • Establishing a class leading QC team leveraging Laboratory Operational Excellence techniques to maximise efficiency during both process qualification and business as usual activities. Show less

    • Product Quality Leader
      • Mar 2011 - Jun 2015

      Leading transformational quality improvement projects for both major assets and new technologies. Major achievements include; • Remediating of 2 key products using Quality Risk Management techniques to implement effective product control strategies thereby mitigating quality and supply risks and reducing waste. Delivered annual savings of over 1M GBP. • Leading a project across more than 50 sites supplying markets in climatic Zone IV to ensure appropriate stability data were available. Where risks were identified a programme of mitigating actions was implemented. Project eliminated compliance risk, ensured continuity of supply and enabled progression of market expansion strategy. • Creating control philosophies for both continuous manufacturing and bio-transformation technologies to facilitate introduction of these transformational technologies into manufacturing. • Leading US-FDA Pre-Approval inspection preparation activities across 6 sites including R&D, Manufacturing and CMOs to achieve successful approval of NCE. • Providing Quality guidance and leadership during design phases for 100M GBP project to build a factory on greenfield site in India. Show less

    • Site Quality Director
      • Sep 1999 - Mar 2011

      Site Quality Director leading a Quality Department of 150 staff supporting a complex vertically integrated manufacturing site supplying over 100 markets including EU, US and Japan. Major achievements include; • Leadership of QA Department through changes associated with major transformation of site activities. • Quality leadership for antibiotic ‘network transformation’ project requiring multiple product transfers to consolidate production from 5 to 2 sites. • Establishing a Penicillin Stability Testing Hub centralising stability testing activities for 3 sites. Show less

Education

  • King's College London
    BSc, Chemistry
  • Kingston University
    MSc, Analytical Chemistry
  • University of Brighton
    PGDip, Industrial Pharmaceutical Studies

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