Gary Shemaka Email
Director Global RA-CMC (Consultant) @ Merck
Lansdale, Pennsylvania, United States
Gary Shemaka's Work
- Director Global RA-CMC (Consultant) @ Merck
- Global Reg. Affairs-CMC, External Manufacturing (Consultant) @ Ispen Biopharmaceuticals
- Global Reg. Affairs-CMC, Dossier Development and Operations (Consultant) @ Janssen Pharmaceuticals R&D, Spring House, PA
- Associate Director-Global Regulatory Affairs (FT) @ Genzyme Corporation (A Sanofi Company)
- RA-CMC Integration Office at Merck Sharp and Dohme (Consultant) @ Genpact Pharmalink
- RA-CMC Recombinant Monoclonal Antibody (Consultant) @ ImClone LLC (Subsidiary of Eli Lilly and Company)
- RA-CMC for Recombinant Therapeutic Proteins (Consultant) @ Genzyme Corporation
- Global RA-CMC Manager Life Cycle Management Support for Small Molecules Products (FT) @ Pfizer Inc.,
- Global RA-CMC Life Cycle Management for Animal Health Science (FT) @ Pfizer
- Associate Director Regulatory Affairs (FT) @ Guilford Pharmaceuticals, Inc. (acquired by Eisia Company),
Gary Shemaka's Education
- Rutgers University, New Brunswick, NJ, Master of Science, Food Science and Engineering
Ohio State University, Columbus, OH, Bachelor of Science, Microbiology (Food Science, Chemical Engineering and Pharmaceutical Packaging)
Gary Shemaka's Skills
- Customer Service
- European Union
- Management
- Aseptic/Conventional Dosages
- Strategic Planning
- Highly Qualified
- Validation
- Results Driven Pharmaceutical Executive
- Training
- u.s. Food and Drug Administration Fda
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