Mahesh Daudia
Validation Engineer at BWXT Canada Ltd- Claim this Profile
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Bio
Antony Appleyard
Mahesh and I worked in cross functional groups to transfer cGMP protein purification processes from the States to the UK. Mahesh was excellent at identifying potential problems and offering timely solutions, demonstrating a high level of professionalism at all times. Mahesh is a great team player and working with him was a great experience.
Eanna Mac Craith
I have had the preasure of both knowing and working with Mahesh. We worked together at Centocor and I was impressed with Mahesh's dedication to the job and his attention to detail. I would work with Mahesh again and recommend him highly
Antony Appleyard
Mahesh and I worked in cross functional groups to transfer cGMP protein purification processes from the States to the UK. Mahesh was excellent at identifying potential problems and offering timely solutions, demonstrating a high level of professionalism at all times. Mahesh is a great team player and working with him was a great experience.
Eanna Mac Craith
I have had the preasure of both knowing and working with Mahesh. We worked together at Centocor and I was impressed with Mahesh's dedication to the job and his attention to detail. I would work with Mahesh again and recommend him highly
Antony Appleyard
Mahesh and I worked in cross functional groups to transfer cGMP protein purification processes from the States to the UK. Mahesh was excellent at identifying potential problems and offering timely solutions, demonstrating a high level of professionalism at all times. Mahesh is a great team player and working with him was a great experience.
Eanna Mac Craith
I have had the preasure of both knowing and working with Mahesh. We worked together at Centocor and I was impressed with Mahesh's dedication to the job and his attention to detail. I would work with Mahesh again and recommend him highly
Antony Appleyard
Mahesh and I worked in cross functional groups to transfer cGMP protein purification processes from the States to the UK. Mahesh was excellent at identifying potential problems and offering timely solutions, demonstrating a high level of professionalism at all times. Mahesh is a great team player and working with him was a great experience.
Eanna Mac Craith
I have had the preasure of both knowing and working with Mahesh. We worked together at Centocor and I was impressed with Mahesh's dedication to the job and his attention to detail. I would work with Mahesh again and recommend him highly
Experience
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BWXT Canada Ltd
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Oil and Gas
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200 - 300 Employee
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Validation Engineer
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Jan 2021 - Present
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GSK
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United Kingdom
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Pharmaceutical Manufacturing
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700 & Above Employee
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Validation Specialist
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Jun 2020 - Dec 2020
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Kite Pharma
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United States
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Biotechnology Research
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700 & Above Employee
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Qualification & Validation
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Mar 2019 - Dec 2019
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Sanofi
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France
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Pharmaceutical Manufacturing
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700 & Above Employee
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Commissioning & Qualification
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Jun 2018 - Dec 2018
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MSD Merck Sharp & Dohme GmbH
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Burgwedel, Germany
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Validation Consultant
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Oct 2016 - Jul 2017
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Akorn India
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Poanta Sahib, India
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Validation Consultant
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Apr 2016 - Sep 2016
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Smith+Nephew
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United Kingdom
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Medical Equipment Manufacturing
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700 & Above Employee
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Validation Engineer
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Aug 2015 - Apr 2016
Phase I:remediation project following FDA inspection. Provide validation/qualification support for facilities, utilities, equipment and processes. Phase II: review, update implement SOPs, gap analysis of current validation/qualification and complete all outstanding Phase I activities. Phase I:remediation project following FDA inspection. Provide validation/qualification support for facilities, utilities, equipment and processes. Phase II: review, update implement SOPs, gap analysis of current validation/qualification and complete all outstanding Phase I activities.
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C.A.F-D.C.F (Red Cross)
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Brussels Area, Belgium
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Quality Consultant
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Apr 2014 - Mar 2015
Primarily providing quality input for a number of projects, including, system qualification, software, cleaning, process, laboratories, cold chain validation for inter and intra site. Primarily providing quality input for a number of projects, including, system qualification, software, cleaning, process, laboratories, cold chain validation for inter and intra site.
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Biocartis
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Belgium
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Medical Device
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200 - 300 Employee
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Quality Engineer
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Apr 2013 - Dec 2014
Supporting qualification and validation activities on site. Updating and implementing new quality system documentation inline with current regulatory requirements. Supporting qualification and validation activities on site. Updating and implementing new quality system documentation inline with current regulatory requirements.
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The Janssen Pharmaceutical Companies of Johnson & Johnson
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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NPI Tech Transfer (Consultant)
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2012 - 2012
QA support for all activities associated with downstream technology transfer for Stelera CNTO1275. QA support for all activities associated with downstream technology transfer for Stelera CNTO1275.
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Crucell
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Biotechnology Research
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1 - 100 Employee
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QA Tech Support Consultant
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2011 - 2012
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Abbott
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United States
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Hospitals and Health Care
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700 & Above Employee
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Validation Consultant
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2009 - 2010
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OctoPlus
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Netherlands
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Quality Assurance / Validation SME
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2009 - 2009
Quality Assurance - Support manufacture of clinical trial products from QA agreement with client to approval of CoA for final product. Including manufacturing documents (batch records), deviations, change control and analytical methods and associated documentation. Validation SME - to advise and/or implement and close out validation issues (plant and process) for the new facility. Quality Assurance - Support manufacture of clinical trial products from QA agreement with client to approval of CoA for final product. Including manufacturing documents (batch records), deviations, change control and analytical methods and associated documentation. Validation SME - to advise and/or implement and close out validation issues (plant and process) for the new facility.
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Centocor
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Biotechnology Research
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400 - 500 Employee
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Lead Engineer
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2008 - 2008
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GSK
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United Kingdom
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Pharmaceutical Manufacturing
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700 & Above Employee
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Validation Engineer
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2007 - 2008
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Centocor
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Biotechnology Research
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400 - 500 Employee
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Quality Assurance Validation Officer
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2007 - 2007
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Abbott
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United States
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Hospitals and Health Care
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700 & Above Employee
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Validation/QA
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Feb 2003 - Aug 2005
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Education
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1994 - 1998
University of East London
bsc, microbiology -
2000 - 2002
King's College London
Molecualr Biology and Biochemistry
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