David Lucero
Associate Director Operational Quality | New Product Introduction NPI@ GSK
Baltimore, Maryland, United States
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David Lucero is a highly experienced professional with over 30 years of expertise in cGMP biopharmaceutical environments. He has a proven track record of building and leading successful teams in Quality, Manufacturing, and Validation. David has successfully executed numerous goals including manufacturing mAb products, release of commercial and clinical drug substance, and continuous improvement projects. His specialties include Quality Assurance, Validation, and Biopharma Manufacturing. He has held various managerial positions at GSK and Human Genome Sciences, demonstrating his leadership and expertise in the pharmaceutical industry. David is currently based in the United States.
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Emails and Phone Numbers

@herontx.com
@gskbio.com
@gsk.com
@gmail.com
@herontx.com
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About

More than 30 years of experience in cGMP biopharmaceutical environments with a proven track record of building and leading successful teams in Quality, Manufacturing and Validation. Successfully executed a broad range of goals including manufacture of mAb products, release of commercial and clinical drug substance, and continuous improvement projects. Specialties: Quality Assurance, Validation, Biopharma Manufacturing

Work Experience

980 Great West Road, Brentford, Middlesex, TW8 9GS, GB

Pharmaceutical Manufacturing

103019
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David Lucero's Professional Milestones

  • Qa Supervisor (2006-01-01~2010-01-01): Implemented effective quality assurance processes, exceeding targets and ensuring compliance with industry standards.
  • Qa Specialist (2003-01-01~2006-01-01): Developing and implementing quality assurance strategies to enhance product safety and customer satisfaction.
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Education

University of Maryland
University of Maryland

Biochemistry

1984-1989