VIce President Quality at Gilead Sciences
Greater New York City Area
Lederle Laboratories
Methods Development Chemist
May 1985 to April 1986
Warner Lambert
Director Product Development
March 1990 to September 1992
Schering-Plough Pharmaceuticals
Manager Methods Development
May 1988 to October 1988
ACT Labs LLC
Chief Operating Officer
Gilead Sciences
Senior Vice President Quality
August 2014 to November 2019
Foster City, California
McNeil Consumer & Specialty Pharmaceuticals
VP Compliance
February 2010 to June 2010
McNeil Consumer & Specialty Pharmaceuticals
VP QA OTC
August 2004 to February 2010
Pfizer
Sr. Director/ US Area Quality Operations Leader
May 2002 to August 2004
Pfizer
Sr. Director Global Quality Analytical Rescources
April 2000 to May 2002
Warner Lambert
VP Worldwide Quality Design
April 1999 to April 2000
Warner Lambert
Sr. Director Analytical Technology
March 1993 to April 1999
Bayer
Dir Product Development
September 1992 to March 1993
Applied Analytical Industries
Director Lab Operations
April 1986 to March 1990
đź“– Summary
Methods Development Chemist @ Lederle Laboratories From May 1985 to April 1986 (1 year) Director Product Development @ Warner Lambert Supervised group of Analytical Chemists responsible for the development of analytical methods in support of new drug entities From March 1990 to September 1992 (2 years 7 months) Manager Methods Development @ Schering-Plough Pharmaceuticals Led group responsible for the development of analytical methods to support new drug products From May 1988 to October 1988 (6 months) Chief Operating Officer @ ACT Labs LLC Multi-state lab network supporting the testing of Cannabis products Senior Vice President Quality @ Gilead Sciences From August 2014 to November 2019 (5 years 4 months) Foster City, CaliforniaVP Compliance @ McNeil Consumer & Specialty Pharmaceuticals Transitioning ongoing day to day activities throughout Johnson and Johnson QA network as part of network consolidationLeading the investigation on a global packaging supplier issue From February 2010 to June 2010 (5 months) VP QA OTC @ McNeil Consumer & Specialty Pharmaceuticals Designed and implemented Quality Systems within McNeilEstablished collaborative relationships with multiple FDA district officesHave direct oversight of 7 plants and approximately 600 quality professionalsCo-lead integration of Pfizer Consumer Healthcare businessPart of 10 Person team (reporting to J&J CEO) defining new cross sector supply chain From August 2004 to February 2010 (5 years 7 months) Sr. Director/ US Area Quality Operations Leader @ Pfizer Responsible for Quality operations for 18 manufacturing sites in US and PRSupervised more than 2000 quality personnel relative to all quality matters at the sitesAccountabke for the full breadth of Pfizer product portfolio including Rx, OTC, active pharmaceutical ingredients, Consumer and sterile productsHAd frequent interactions with FDA and other regulatory agencies From May 2002 to August 2004 (2 years 4 months) Sr. Director Global Quality Analytical Rescources @ Pfizer Responsible for Techincal Services group for PfizerHad global responsibility for providing all analytical services support including stability testing, analytical methods transfer, troubleshooting, counterfeit testingSupervised group of over 200 colleagues located in 2 locations From April 2000 to May 2002 (2 years 2 months) VP Worldwide Quality Design @ Warner Lambert Lead tecjnology Support Center for Warner Lambert on a global basisResponsible for implementing globalized standards to ensure compliance in laboratories around the worldManaged a group of 110 personsResponsible for troubleshooting for all analytical methods used globallyHad multiple FDA interactions with San Juan PR, Parsippany/Newark, Philadelphia and Detroit district offices From April 1999 to April 2000 (1 year 1 month) Sr. Director Analytical Technology @ Warner Lambert Supervised group responsible for the revalidation of all analytical methods used to test products in North AmericaChief contact with FDA on all analytical issuesMet weekly with FDA during early stages of Consent DecreeResponsible for the start-up of Central Stability Laboratory From March 1993 to April 1999 (6 years 2 months) Dir Product Development @ Bayer Led the startup of analytical and formualtions group to support new product development in the USResponsible for technical content of all NDA's submitted to FDA From September 1992 to March 1993 (7 months) Director Lab Operations @ Applied Analytical Industries Responsible for the start up of an analytical methods development and testing lab (group expanded from 4-75 chemists)Chief FDA contact for all technical issuesResponsible for the start up of Formulations Development Division From April 1986 to March 1990 (4 years)
What company does Robert Miller work for?
Robert Miller works for Lederle Laboratories
What is Robert Miller's role at Lederle Laboratories?
Robert Miller is Methods Development Chemist
What industry does Robert Miller work in?
Robert Miller works in the Pharmaceuticals industry.
Who are Robert Miller's colleagues?
Robert Miller's colleagues are John Barcelona, Lynette Manderson, Valerie Chidiac, Lisa Liao, Miet Janssens, Marijn Nivelle, Julie Medeiros, Yeshwanth Raj, James O'Regan, and MATTIA SIYNARDI
Extraversion (E), Intuition (N), Feeling (F), Judging (J)
2 year(s), 7 month(s)
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