Ken Hoglund is a highly qualified professional, that works in Theravance Biopharma Us, Inc main office of which is in 1092. as a Director Gcp and Glp Quality Assurance from 2016. Ken gained professional experience in more than ten positions at different companies. Ken Hoglund went to the University of Strathclyde and received education there from 2009 to 2012. Santa Rosa, California is the city, where the professional was lastly known to be living. Ken's email address and phone number are accessed through this website on demand.
Name variants:
Kendall Hoglund,
Kendrick Hoglund,
Kenneth Hoglund,
Kent Hoglund
Last updated May 29, 2024
Contact Information
Last Update
Jul 7, 2022
Email
ke**@talecris.com, kh**@herontx.com
Location
Santa Rosa, CA
Company
Theravance Biopharma Us, Inc.
Workplace
Director Gcp and Glp Quality Assurance
Work History
Director Gcp and Glp Quality Assurance
901 Gateway Blvd, South San Francisco, CA 94080
Apr 2016 — Mar 2019
Vice President of Compliance, Quality Assurance and Quality Control
4242 Campus Point Ct SUITE 200, San Diego, CA 92121
Provided QA and QC program Quality and Compliance oversight for Development and Manufacturing activities. Covering cGMP, GCP, GLP, and Device requirements.
May 2013 — Oct 2014
Director R and D Compliance
Clinical and Preclinical compliance oversight for biological products and medical devices in Development,
Jun 2011 — Mar 2013
Director R and D Qa
North Carolina
Served as member of R&D Sr Management team. Lead all aspects of compliance program design and implementation of Quality Management Systems for Clinical and PreClinical biologics and devices ...
Jun 2005 — Jun 2011
Manager, Corporate Compliance
Responsible for design and implementatoin of Corporate Quality change efforts in manufauring and R&D. Responsible for Corporate policy development and implementation specific to Engineering,...
May 2003 — May 2006
Product Quality Manager
Oversee QA activities for Process Validation, Facility Qualification submissions review and licensing of new sterile fill facility, manage ongoing commercial production filling activities, u...
2001 — 2003
Project Manager R and D
Support key change projects related to merger of GW and SKB ie High-throughput screening redesign (combine process, technology, and sample management for WW HTS in R&D), International Analyt...
Feb 2000 — Apr 2001
Manager, Technical Services and Instrumentation
Managed start-up and ongoing operations for analytical laboratory and process scale-up instrumentation services at multiple sites for Glaxo/GW/GSK
Apr 1992 — Mar 2001
Senior Manager Technical Support
Start up for pharma technical support in the areas of laboratory and pilot plant instrumentation, integration, calibration, qualification from R&D to Manufacturing
May 1986 — May 1992
Senior Research Associate, Analytical and Qc
Analytical Chemist in drug development and QC
for parenterals and OTC products
Research Biochemist for GLP studies
Mar 1981 — May 1986
Education
2009 — 2012
1997 — 1998
1975 — 1979
Occupations
IT Professional
Software Tester
Executive
Director
Vice President
Computer Specialist
Operations Manager
Chief Executive
Skills
R&D
Technology Transfer
Quality Assurance
Life Sciences
Manufacturing
Managing Change
Change Management
Validation
Medical Devices
Quality System
Glp
Lifesciences
Biotechnology
Iso 13485
Regulatory Affairs
V&V
Fda
Chemistry
Sop
Change Control
Gxp
21 Cfr Part 11
Gmp
Computer System Validation
Biopharmaceuticals
Pharmaceutical Industry
Biochemistry
Laboratory
Capa
Lims
Drug Development
Testing
Quality Control
Clinical Development
Aseptic Processing
Pharmaceutics
Records Management
Global Regulatory Compliance
Analytical Chemistry
Knowledge Management
Risk Management
Gcp
Quality Auditing
Chromatography
Design Control
Biologics
Fda Gmp
Quality Management
Cgmp Practices
Clinical Trials