Director Of Regulatory Affairs, Us Regional Regulatory Lead, Cardiometabolism
Current
Jun 2021 - Present
AeroLeads people directory · profile
Mark Debellis Email & Phone Number
Director at Boehringer Ingelheim
at
Boehringer Ingelheim
1 work email found
@boehringer-ingelheim.com
LinkedIn matched
✓ Verified May 2026
4 data sources
Profile completeness 100%
Current company
Role
Director at Boehringer Ingelheim
Location
Ridgefield, Connecticut, United States
Who is Mark Debellis? Overview
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Quick answer
Mark Debellis is listed as Director at Boehringer Ingelheim at Boehringer Ingelheim, based in Ridgefield, Connecticut, United States. AeroLeads shows a work email signal at boehringer-ingelheim.com and a matched LinkedIn profile for Mark Debellis.
Mark Debellis previously worked as Director of Regulatory Affairs, US Regional Regulatory Lead, Cardiometabolism at Boehringer Ingelheim and Senior Associate Director, Regulatory Affairs; US Regional Regulatory Lead Cardiometabolism at Boehringer Ingelheim. Mark Debellis holds Master Of Science - Ms, Industrial Pharmacy/Pharmaceutics from Liu - Arnold And Marie Schwartz College Of Pharmacy.
Company email context
Email format at Boehringer Ingelheim
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{first}.{last}@boehringer-ingelheim.com
86% confidence
AeroLeads found 1 current-domain work email signal for Mark Debellis. Compare company email patterns before reaching out.
Profile bio
About Mark Debellis
Mark Debellis is a Director at Boehringer Ingelheim at Boehringer Ingelheim. He possess expertise in cmc regulatory affairs, gmp, validation, sop, gxp and 22 more skills.
Listed skills include Cmc Regulatory Affairs, Gmp, Validation, Sop, and 23 others.
Current workplace
Mark Debellis's current company
Company context helps verify the profile and gives searchers a useful next step.
11 roles · 33 years
Mark Debellis work experience
A career timeline built from the work history available for this profile.
Senior Associate Director, Regulatory Affairs; Us Regional Regulatory Lead Cardiometabolism
Jun 2017 - Jun 2021
Senior Associate Director, Cmc Regulatory Affairs
Jul 2014 - Jun 2017
Associate Director, Cmc Regulatory Affairs
Apr 2010 - Jul 2014
Manager, Cmc Regulatory Affairs
Jan 2007 - Apr 2010
Associate Director, Cmc Regulatory Affairs
Boehringer-Ingelheim
Apr 2010 - Jun 2014
Validation Specialist
2004 - 2006
~2 yrs
Validation Specialist
Purdue Pharma Lp (Purdue Fredrick)
2001 - 2004
~3 yrs
Validation Specialist
Purdue Pharma
2000 - 2004
~4 yrs
Scientist, Pharmaceutical Analysis
1996 - 2000
~4 yrs
Scientist, Physical Chemistry
1993 - 1996
~3 yrs
2 education records
Mark Debellis education
Master Of Science - Ms, Industrial Pharmacy/Pharmaceutics
Liu - Arnold And Marie Schwartz College Of Pharmacy
Bs, Biochemistry
Pace University-Pleasantville/Briarcliff Campus
FAQ
Frequently asked questions about Mark Debellis
Quick answers generated from the profile data available on this page.
What company does Mark Debellis work for?
Mark Debellis works for Boehringer Ingelheim.
What is Mark Debellis's role at Boehringer Ingelheim?
Mark Debellis is listed as Director at Boehringer Ingelheim at Boehringer Ingelheim.
What is Mark Debellis's email address?
AeroLeads has found 1 work email signal at @boehringer-ingelheim.com for Mark Debellis at Boehringer Ingelheim.
Where is Mark Debellis based?
Mark Debellis is based in Ridgefield, Connecticut, United States while working with Boehringer Ingelheim.
What companies has Mark Debellis worked for?
Mark Debellis has worked for Boehringer Ingelheim, Boehringer-Ingelheim, Pfizer, Purdue Pharma Lp (Purdue Fredrick), and Purdue Pharma.
How can I contact Mark Debellis?
You can use AeroLeads to view verified contact signals for Mark Debellis at Boehringer Ingelheim, including work email, phone, and LinkedIn data when available.
What schools did Mark Debellis attend?
Mark Debellis holds Master Of Science - Ms, Industrial Pharmacy/Pharmaceutics from Liu - Arnold And Marie Schwartz College Of Pharmacy.
What skills is Mark Debellis known for?
Mark Debellis is listed with skills including Cmc Regulatory Affairs, Gmp, Validation, Sop, Gxp, 21 Cfr Part 11, Fda, and Capa.
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