Laura Murphy Email & Phone Number | I am a Continuous Improvement owner at Amgen, which includes ownership of the CAPA Process Team, Cross Functional Projects, Problem Solving oversight, Nonconformance proactive trending, and oversight of Safety and Risk governance of our manufacturing site at Amgen Thousand Oaks. I support a research, clinical and commercial facility, through use of my knowledge of the biopharmaceutical process to develop and shape appropriate and effective changes that impact molecule processes, the facility and/or business. I continue to lend my manufacturing and managerial experiences to other departments in various improvement projects. I have been in the scientific industry for 17 years moving from peptides and cell culture QC assay development, to R&D pilot manufacturing, clinical and commercial manufacturing as a manager and now CAPA SME, project owner and Continuous Improvement Lead. I am ever evolving in the response of industry and embrace change.

Laura Murphy

I am a Continuous Improvement owner at Amgen, which includes ownership of the CAPA Process Team, Cro...
2777 Waverly Court, Camarillo, United States

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Laura Murphy’s Email laura.murphy@amgen.com

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Laura Murphy’s Location 2777 Waverly Court, Camarillo, United States

Laura Murphy’s Current Industry Amgen

Laura Murphy’s Prior Industry Yoh Services For Amgen | Life Technologies | Molecular Epidemiology

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Manufacturing Specialist

2019-02-01 00:00:00 - Present

Cell Culture Associate Scientist II

2010-11-01 00:00:00 - 2011-03-01 00:00:00

Sr. Manufacturing Support Coordinator

2007-07-01 00:00:00 - 2010-11-01 00:00:00

Quality Analyst I

2007-02-01 00:00:00 - 2007-07-01 00:00:00

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Laura Murphy is a I am a Continuous Improvement owner at Amgen, which includes ownership of the CAPA Process Team, Cross Functional Projects, Problem Solving oversight, Nonconformance proactive trending, and oversight of Safety and Risk governance of our manufacturing site at Amgen Thousand Oaks. I support a research, clinical and commercial facility, through use of my knowledge of the biopharmaceutical process to develop and shape appropriate and effective changes that impact molecule processes, the facility and/or business. I continue to lend my manufacturing and managerial experiences to other departments in various improvement projects. I have been in the scientific industry for 17 years moving from peptides and cell culture QC assay development, to R&D pilot manufacturing, clinical and commercial manufacturing as a manager and now CAPA SME, project owner and Continuous Improvement Lead. I am ever evolving in the response of industry and embrace change.