Ray Ormiston Email & Phone Number
@gsk.com
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Who is Ray Ormiston? Overview
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Ray Ormiston is listed as Director CMC Regulatory Affairs at GlaxoSmithKline at GlaxoSmithKline, based in Stevenage, England, United Kingdom. AeroLeads shows a work email signal at gsk.com and a matched LinkedIn profile for Ray Ormiston.
Ray Ormiston previously worked as Retired at Retired Cmc Regulatory Director At Gsk and Director CMC Regulatory Affairs at Glaxosmithkline.
Email format at GlaxoSmithKline
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AeroLeads found 2 current-domain work email signals for Ray Ormiston. Compare company email patterns before reaching out.
About Ray Ormiston
Ray Ormiston is a Director CMC Regulatory Affairs at GlaxoSmithKline at GlaxoSmithKline. He possess expertise in pharmaceutical industry, regulatory affairs, regulatory submissions, gmp, clinical trials and 11 more skills.
Listed skills include Pharmaceutical Industry, Regulatory Affairs, Regulatory Submissions, Gmp, and 12 others.
Ray Ormiston's current company
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Ray Ormiston work experience
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Director Cmc Regulatory Affairs
Current
Regulatory Affairs Professional
Synthetic Chemist
Frequently asked questions about Ray Ormiston
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What company does Ray Ormiston work for?
Ray Ormiston works for GlaxoSmithKline.
What is Ray Ormiston's role at GlaxoSmithKline?
Ray Ormiston is listed as Director CMC Regulatory Affairs at GlaxoSmithKline at GlaxoSmithKline.
What is Ray Ormiston's email address?
AeroLeads has found 2 work email signals at @gsk.com for Ray Ormiston at GlaxoSmithKline.
Where is Ray Ormiston based?
Ray Ormiston is based in Stevenage, England, United Kingdom while working with GlaxoSmithKline.
What companies has Ray Ormiston worked for?
Ray Ormiston has worked for Retired Cmc Regulatory Director At Gsk, Glaxosmithkline, Gsk, and Sterling-Winthrop.
How can I contact Ray Ormiston?
You can use AeroLeads to view verified contact signals for Ray Ormiston at GlaxoSmithKline, including work email, phone, and LinkedIn data when available.
What skills is Ray Ormiston known for?
Ray Ormiston is listed with skills including Pharmaceutical Industry, Regulatory Affairs, Regulatory Submissions, Gmp, Clinical Trials, Clinical Development, Fda, and Validation.
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