Michael Kelliher is a eficient professional, who works in 3Dbio Therapeutics main office of which is in 308. as a Senior Director of Manufacturing from 2019. This person gained professional experience in more than five positions at various companies. Michael Kelliher went to the Nyu Stern School of Business and was studying from 2012 to 2014. New York, New York is the area, where this professional was known to be situated. This professional's phone number and email are easily accessed through SoftwareOfficial on demand.
Name variants:
Mikael Kelliher,
Mychael Kelliher,
Mike Kelliher,
Mikey Kelliher,
Mick Kelliher,
Mickey Kelliher,
Micky Kelliher,
Michl Kelliher,
Mischa Kelliher
Last updated Jun 07, 2024
Contact Information
Last Update
Jul 10, 2022
Email
mi**@yahoo.com, mk**@ispe.org
Location
New York, NY
Company
3Dbio Therapeutics
Workplace
Senior Director of Manufacturing
Work History
Senior Director of Manufacturing
51-36 35Th St, Long Island City, NY 11106
from Jul 2019
Director of Manufacturing
50 Binney St, Cambridge, MA 02142
Responsible for Syringe Formulation/Fill/Finish Interim responsibility for Capital Project Management
Nov 2004 — Jul 2019
Vice President, Nj Chapter Board of Directors
6110 Executive Blvd SUITE 600, North Bethesda, MD 20852
ISPE, the International Society for Pharmaceutical Engineering, is the world's largest not-for-profit association serving its Members through leading scientific, technical and regulatory adv...
Jul 2014 — Jul 2019
Director of East Coast Operations
11 north Skokie Hwy, Lake Bluff, IL 60044
Provided validation consulting to the pharmaceutical, biotech, and medical device industries
Jun 2001 — Nov 2004
Supervisor, Sterilization Engineering Group
Illinois
Directed sterilization equipment qualification initiative for the diagnostic division
Oct 1996 — Jun 2001
Education
2012 — 2014
1992 — 1996
Occupations
Executive
Senior Director
Scientist
Biotechnology Professional
Director
Senior Manager
Operations Manager
Biologist
Biological Scientist
Skills
Biotechnology
Fda
Gmp
Pharmaceutical Industry
Biopharmaceuticals
Validation
Medical Devices
Regulatory Requirements
Sop
21 Cfr Part 11
Technology Transfer
Change Control
Computer System Validation
Clinical Development
Quality Assurance
Capa
U.s. Food and Drug Administration
Standard Operating Procedure