Evan Bekos
Director, GQAS&T at Bristol Myers Squibb
- Role
- Director, Global Quality Analytical Science & Technology at Bristol Myers Squibb
- Location
- New York, NY, US
- LinkedIn followers
- 500 followers
About Evan Bekos
PHARMACEUTICAL PROFESSIONALAnalytical Development CMO Managament Laboratory Management CMC/Regulatory Proven, forward-thinking, leader with a blend of “big pharma” and small biotech experience. Comprehensive knowledge of the drug development process through regulatory approval, including post-approval technical support. Extensive experience in managing analytical laboratory operations, overseeing with third party manufacturers (CMOs), technology transfer, and regulatory guidelines. Wrote and reviewed CMC sections of global regulatory documents and responded to health authority inquiries. Core team member of integrated development teams that set strategy to drive drug development, CMC timelines and regulatory strategy. Strong leadership skills, with over 12 years of direct managerial experience focused on developing talent and building highly effective teams. Responsible for performance reviews and development plans. Detail oriented with the ability to see the big picture. Demonstrated success working with different cultures and with many business areas.Core Competencies Analytical laboratory operations Talent Management and Development Cross-functional CMC development teams CRO/CMO management Analytical methodology & validation Technology Transfer Regulatory filings and compliance
Experience
Director, Global Quality Analytical Science & Technology
Nov 2019 — Present · Summit, NJ, US
Education
State University of New York at Oswego
Bachelor of Science (B.S.), Chemistry
State University of New York at Oswego
Master of Science (M.S.), chemistry
University at Buffalo
Ph.D, Analytical Chemistry
Skills
- Technology Transfer
- Regulatory Submissions
- Uv/Vis
- Lc-Ms
- Dissolution
- Organic Chemistry
- Chromatography
- Spectroscopy
- Chemistry
- Good Laboratory Practice (Glp)
- Hplc
- High-Performance Liquid Chromatography (Hplc)
- Gmp
- Pharmaceutical Industry
- Sop
- Nmr
- Validation
- Mass Spectrometry
- Medicinal Chemistry
- Drug Development
- Analytical Chemistry
- Glp
- Drug Discovery
- Organic Synthesis
- Standard Operating Procedure (Sop)
- Lims
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