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Responsible for delivery of GCP & PV QA for all American, European, SE Asian, African & Australian projects.
Aubrey & Aubrey Associates Ltd
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Vice PresidentAubrey & Aubrey Associates Ltd Mar 2023 - PresentLondon, England, United KingdomFormation of Consultancy to best advise and help Pharma in fulfilling ethical and legal parameters of clinical trials internationally
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1-Aug-2024 = 45 Years In Pharma For Me!Assorted Aug 1979 - Present
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Senior Director, Quality AssuranceMitsubishi Tanabe Development America Inc. Apr 2018 - Nov 2022Jersey City, New Jersey, UsaAllocated additional responsibility for IMP-GMP QA in Americas.
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Senior Director Of Quality AssuranceMitsubishi Tanabe Development America Inc. Jan 2016 - Nov 2022Jersey City, New Jersey, UsaFollowing departure of previous incumbent my role has expanded in that I am now also responsible for the delivery of GCP & PV Quality to the Mitsubishi-Tanabe USA affiliate.
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General Manager, Head Of QaMitsubishi Tanabe Pharma Europe May 2013 - Nov 2022London, UkWorking with my team, I am responsible for all European GCP and PV QA activities. Integrating closely with my Japan colleagues to create mutually global, aligned GCP and PV QA systems.
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Senior Director Qa Gcp/GlpDaiichi Sankyo Sep 2011 - Apr 2013Gerrards Cross, BucksResponsible for all GCP & GLP Compliance (non-Japan) for Europe, India and Americas
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Interim Gcp ManagerDainippon Sumitomo Aug 2011 - Sep 2011Victoria, LondonShort term position to hold QA initiatives in place control SOP system, training matrices etc
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Consultant At Large!Consultant Jan 2011 - Sep 2011London, United KingdomBrief time between full-time contracts undertaking 4 quite different roles [at CliniRx, MedImmune, DaiNippon Sumitomo and RetroScreen Virology].
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Interim Gcp Qa ManagerRetroscreen Virology Jun 2011 - Aug 2011Whitechapel, LondonDuring this assignment I managed nearly all GCP related activity in this phase 1 virology clinic -
Interim Gcp Inspection CoordinatorMedimmune Feb 2011 - May 2011Cambridge, UkIn this time I managed GCP Inspection preparatory activity across all regions and all departments through to managing Inspection itself and eventual outcome.
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Qa AssociateClinirx Jan 2011 - Mar 2011Stockley ParkShort assignment to review all SOPs within system and to propose changes to make SOPs truly global.
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Senior DirectorTakeda Global R&D Europe Apr 2002 - Jan 2011London, United KingdomWell now, I am responsible for the QA of all GxPs in what Takeda defines as Europe; Iceland to New Zealand, Siberia to South Africa - so I do quite a bit of travelling here and there - but, the rest of the time I live and am based in Central London; so if any "old" colleague is ever up here 'in the smoke' why not catch up?! Best Regards to all, Mark
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Gcp Committee ChairmanBarqa 2002 - 2005Ipswich, United KingdomI chaired the BARQA GCP Committee for 3 years instigating many initatives such as separate GCP streams at conferences, controlled Q&A system, and interim teleconferences. Role was wide and varied and included also, board meetings.
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Associate Director Gcp QaElan May 2000 - Apr 2002Stevenage, United KingdomProbably my most interesting therapeutic area, not just MS (for the 3rd time!), but Migraine and, my all time favourite - Epilepsy. Company was small then and growing rapidly set up 1st ever SOP system there and took it [I think] to the next level before their financial pressures took hold.. -
Worldwide Gcp Audit ManagerMerck Serono Jan 2000 - Apr 2000Geneva Area, SwitzerlandAn interesting time with my 2nd company looking at MS development - lots of travel, but working at an HQ, in Geneva was an altogether different experience -
Gcp Audit ManagerSchering Health Care Ltd Jan 1990 - Jan 2000Burgess Hiil, UkThis role took me from lab-rat to monitor (CRA) to auditor to audit management, where I seem to have been ever since. Worked on anxiolytics, OCs, HRT, Oncocology and MS. Spent ten years there whilst married in developing QA systems hosted 2nd ever (voluntary) MHRA GCP Inspection, and a few other things besides - I occassionally still go by the old building in B-Hill, shame to see it looking derelict now.. -
Technical OfficerSmithkline Beecham Aug 1979 - Jan 1990Worthing, West SussexWorthing Site: Fermentation Pilot Plant Support Laboratory, worked in small laboratory analysing samples from microbial fermentations of Clavulanic acid MM14151 (Augmentin) and of Penicillin G, also micobiological support and of a few other microbes besides e.g. streptococcus equisimilus [later better known as Eminase]
Mark Aubrey Skills
Mark Aubrey Education Details
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North East London PolytechnicAnalytical Biochemistry -
Applied Biology -
Worthing Technical CollegeBiology
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Redruth County Grammar SchoolChemistry, Biology, Mathematics
Frequently Asked Questions about Mark Aubrey
What company does Mark Aubrey work for?
Mark Aubrey works for Aubrey & Aubrey Associates Ltd
What is Mark Aubrey's role at the current company?
Mark Aubrey's current role is Head of QA.
What is Mark Aubrey's email address?
Mark Aubrey's email address is ma****@****-eu.com
What is Mark Aubrey's direct phone number?
Mark Aubrey's direct phone number is +4420706*****
What schools did Mark Aubrey attend?
Mark Aubrey attended North East London Polytechnic, Brighton College Of Technology, Worthing Technical College, Redruth County Grammar School.
What are some of Mark Aubrey's interests?
Mark Aubrey has interest in Diy, Opera, Guinness, Donegal, Cornwall, Brighton And Hove Albion Football Club, Married Life.
What skills is Mark Aubrey known for?
Mark Aubrey has skills like Gcp, Sop, Gxp, Pharmaceutical Industry, Quality Assurance, Glp, Clinical Trials, Clinical Development, Pharmaceutics, Cro, Regulatory Submissions, Regulatory Affairs.
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2ssvotech.org, ssvotech.org3 +178187XXXXX
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Mark Aubrey
Senior Director Quality Assurance At Mitsubishi Tanabe Pharma Development AmericaJersey City, Nj1mt-pharma-us.com -
Mark Aubrey
Seymour, Tn1snmp.com -
Mark Aubrey
Retired - Open To Remote, Part Time Work. Professional Liability Claims.Los Angeles Metropolitan Area2msn.com, camico.com1 +165080XXXXX
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