Adam Dunko
Quality Systems Manager@ CTI BioPharma
Seattle, Washington, United States
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Adam Dunko is a highly experienced Quality Assurance professional with 26.3 years of work experience in the pharmaceutical industry. He has expertise in GMP, SOPs and Policies, risk management, and document control. Adam has worked in various roles, including Director of Quality at Sierra Oncology and Associate Director of Quality Management Systems at Acerta Pharma B.V. He has also held positions at CTI BioPharma and GE Healthcare. With a strong background in quality assurance and analytical chemistry, Adam is a valuable asset in the field of pharmaceuticals biotech.
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Colleagues

Emails and Phone Numbers

@ctibiopharma.com
@acerta-pharma.com
@gmail.com
@sierraoncology.com
@ctiseattle.com
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About

Quality Assurance | Pharmaceuticals | Biotech 17 Years of industry experience in GMP/GCP regulated organizations, supporting commercial and clinical products. Quality management systems development, SOPs and Policies, computer system qualification/validation, risk management, document control, change control, deviations, CAPAs, APRs/PQRs, internal and vendor audits, product complaints, quality agreements, regulatory inspections, training systems, electronic quality management system administration, and personnel management.

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Work Experience

3101 Western Ave., #600, Seattle, WA, 98121, US

Biotechnology Research

231
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Adam Dunko's Professional Milestones

  • Senior Manager Quality Assurance (2013-07-01~2016-04-01): Implemented comprehensive quality control measures to ensure product excellence and customer satisfaction.
  • Analytical Stability Chemist (2001-06-01~2002-09-01): Conducted groundbreaking experiments in a new field of analytical stability, expanding the scientific community's understanding and understanding of the
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Education

Stockton University
Stockton University

Chemistry,

Bachelors,

Bachelor Of Science

1992-1998