Mohamed Fouad

New Product Development Project Manager at Brauer Natural Medicine
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Adelaide Area
Languages
  • Arabic Native or bilingual proficiency
  • English -

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William Teags

I have had the pleasure of working with Mohamed on several projects as part of the Johnson & Johnson (J&J) Supplier Quality team. In his role on these projects, Mohamed provided manufacturing, quality, product and process expertise to valuable J&J suppliers, assisting in their efforts to improve the quality of products supplied to J&J. Mohamed has global experience in the pharmaceutical and medical device industries, and his ability to effectively communicate positively as a team leader has proven valuable on numerous occasions. Mohamed is a very reliable, thorough and well-respected resource, and I welcome the opportunity work with him in the future.

mohamed ibrahim

Mohamed Waleed is an excellent man and he have a very good vision

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Credentials

  • Essential and Practical GCP Training for New Monitors and CRAs
    ARCS Australia
    Jun, 2021
    - Nov, 2024
  • Good Clinical Practice
    The National Institute on Drug Abuse (NIDA)
    Aug, 2020
    - Nov, 2024
  • Certified Manager of Quality/Organizational Excellence
    Ammerican Society of Quality
    Oct, 2006
    - Nov, 2024

Experience

  • Brauer
    • Australia
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • New Product Development Project Manager
      • Nov 2019 - Present

      I am driving NPD (New Product Development) process at Brauer Natural Medicine. I have deployed new stage-gate process for the NPD that divide the NPD into (Research brief, feasibility, development, and commercialization). I am driving Continuous Improvement stream that focus on packaging and product formulation improvements based on market feedback. I am working closely with R&D, Operations, Marketing, and Sales teams. Brauer Natural Medicine was known for its homeopathic medicines in Australia since 1929 focusing on domestic market, then started major transformation 5 years back to extend its pipe line with herbal and multivitamins products focusing on new exportation markets in addition to traditional domestic distribution channels. HIGHLIGHTS for my 1year in Brauer: • Launched 2 new Kids products via CBEC (Cross Boarder E-Commerce) in China mainland. • Launched 8 new adult products via CBEC (Cross Boarder E-Commerce) in China mainland. • Led 4 package changes across Brauer products to address continuous improvements. • Led 4 product re-formulations to address continuous improvements. • Led 1 Technology Transfer project for teething gel in-house manufacturing.

  • Pfizer
    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Senior Manufacturing Quality
      • Nov 2018 - Nov 2019

      I led investigations, CAPA, and batch release activities for Pfizer Global Supply Adelaide. Site is part of Pfizer biotech network that is specialized in recombinant protein manufacturing derived from microbial fermentation of genetically modified E.coli. I conducted GMP annual reviews (e.g. Annual Product Quality Review, CAPA annual review, etc.). As certified GMP Auditor, I supported site self assessment program. As part of my role, I am supported production, and other functional areas to help ensure that all manufacturing and related activities are executed in compliance with GMP requirements. HIGHLIGHTS • Managed annual product quality review. • Conducted CAPA annual review. • Conducted Internal audits on various quality systems • Site Quality Authority for batch review/disposition recommendation • Quality approver of manufacturing investigation records. • Represented manufacturing quality in site end to end Tier 2 meetings. • Developed training for “Understanding Biological Analytical Science and Biological Manufacturing Science”

  • Johnson & Johnson
    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Enterprise Staff Supplier Quality
      • Jul 2016 - Apr 2018

      I performed supplier technical assessment process across J&J Enterprise suppliers for direct material suppliers & external manufacturers, supporting (Medical Devices, Pharma, & Consumer) divisions of J&J. Located in Dubai office and reported to global group based in US. I led technical assessments, working with J&J internal and external partners to understand suppliers’ capabilities and areas for improvements.HIGHLIGHTS• I led 30+ process excellence engagements with different Enterprise J&J suppliers in EMEA & ASPAC regions. • I worked with packaging, chemicals, metals, API/Biologics, & external manufacturing suppliers. • I trained/mentored J&J supplier quality engineers on process excellence.• I coordinated various cross functional teams during supplier engagements.• I worked with suppliers to ensure effective and efficient use of Process Excellence tools and Quality Engineering techniques such as risk analysis, statistical data analysis, statistical process control, Human error reduction, etc.

    • Manager Q&C EAME, External Manufacturer
      • Sep 2011 - Jul 2016

      ROLE SUMMARYI managed Quality and compliance of the Middle East North Africa Turkey & Pakistan J&J Consumer External Manufacturers portfolio for OTC/Cosmetic products. Located in regional office in Dubai and reported to EMEA regional group based in France.I supported supplier life-cycle management at various stages; e.g. on-boarding, maintenance, & disengagement. I worked closely with internal J&J EM make folks to ensure supply reliability in case of field actions, major issues/non-conformances.I worked on deploying and implementing J&J Quality initiatives and standards at different External Manufacture plants.HIGHLIGHTSExternal manufacturers (EM)• I led 30+ GMP audits on different EMs located in EMEA. • I negotiated Quality Responsibility Agreement with different EMs to keep the agreement up to date with J&J latest expectations.• I worked with global team for harmonization of source quality core processes across various J&J consumer regions.• I led quality relationship management calls with the suppliers to review KPIs, Management Action Plan, and CAPA follow up.• I coordinated annual global top to top meetings with strategic suppliers for strategic sourcing discussion.• I got one Gold (for product recall management) & one Bronze (for core processes harmonization) Encore Awards on 2016. EMEA Supplier Reliability Project:• I joined cross functional supplier reliability team with EM Make, Sourcing, & Material Supplier Management organizations. Team established and governed a consistent supplier reliability process within the region for both external manufacturers and direct material suppliers utilizing various J&J improvement tools.

  • Sanofi
    • France
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • QA Manager
      • Aug 2010 - Sep 2011

      ROLE SUMMARY I managed Quality Assurance department of Sanofi Cairo plant, had 10 direct reporters and reported to the site quality operations manager. Plant produces Solid, Semi-Solid, Liquid, sterile aseptic filling, & sterile terminally sterilized formulations. HIGHLIGHTS Quality Assurance team: • I managed the department and ensured proper performance of day to day activities: e.g. Finished Products Batch Disposition, Validation Master Planning, Site Self Inspection program, Document control, Investigation management, third party audit program. • I worked on department personnel development planning. Projects: • I led cross functional team from engineering, quality, & production organizations to manage the proper go live of terminally sterilized ampoule area from the facility qualification stage till final regulatory inspection.

  • Eli Lilly and Company
    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Senior QA "Projects"
      • Feb 2009 - Aug 2010

      ROLE SUMMARYEgypt site QA project representative for Eli Lilly global projects, plant dedicated for insulin vials sterile aseptic filling.HIGHLIGHTS• I worked with cross functional global projects team to deliver QC lab & WH for Eli Lilly Egypt site. • I coordinated project governance meeting with local deployment team, global support team, contractor and consultant.• I managed all Commissioning Qualification activities regarding lab & WH.• I led project for personnel Qualification to enhance qualification of critical GMP duties.• I have been awarded the 2009 Global HR Award for the (Personnel Qualification Project)

    • QA Pharmacist
      • Mar 2007 - Feb 2009

      ROLE SUMMARYTeam member of Quality unit in Egypt site, plant dedicated for insulin vials sterile aseptic filling. HIGHLIGHTS• I acted as qualified person for batch disposition.• I led change control system, and change review board.• I acted as site Computer Systems QA, responsible of all Egypt relevant Computer System Validation deliverable approval.• I led the deployment of Lilly Education And Development System (LEADS).• I participated in Lilly CAPA Trackwise Deployment project, acting as the project training coordinator.

  • Ranbaxy
    • India
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • QA Supervisor
      • Sep 2005 - Mar 2007

      ROLE SUMMARY I worked as QA supervisor. I managed the quality relationship between Ranbaxy Egypt and Egyptian toll manufacturers. Product portfolio includes: solid, terminally sterilized ampoule, Powder for suspension formulations. ROLE SUMMARY I worked as QA supervisor. I managed the quality relationship between Ranbaxy Egypt and Egyptian toll manufacturers. Product portfolio includes: solid, terminally sterilized ampoule, Powder for suspension formulations.

  • Alkan Pharma
    • QA Validation Supervisor
      • Dec 2000 - Sep 2005

      ROLE SUMMARY I started my career in pharmaceutical manufacturing in Egyptian private sector Company named Alkan pharma (now called HIKMA Egypt). I have started as part of QA team in the plant as QA officer then QA supervisor. Plant produces Solid, Semi-Solid, & Liquid formulations. ROLE SUMMARY I started my career in pharmaceutical manufacturing in Egyptian private sector Company named Alkan pharma (now called HIKMA Egypt). I have started as part of QA team in the plant as QA officer then QA supervisor. Plant produces Solid, Semi-Solid, & Liquid formulations.

Education

  • University of the Western Cape/Universiteit van Wes-Kaapland
    Master's degree, Pharmacy Administration and Pharmacy Policy and Regulatory Affairs
    2014 - 2018
  • The American University in Cairo
    Diploma, TQM
    2003 - 2004
  • Cairo University
    Batchelor, Pharmaceutical scienece
    1994 - 1999

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