
Monica Puskas
Validation Engineer
About
•13 years experience providing analytical and process support for the development of new R&D products. •1st shift supervisor of analytical laboratory supporting all R&D activities. •Leader of investigations of OOS and unexpected results. •Developed and validated analytical methods for determination of protein purity by HPLC and electrophoresis. •Transferred test methods between laboratories both internally and externally. •Worked on cross-functional R&D project teams to provide analytical test support and prioritization of lab resources. •Project Team Leader of a cross-functional team to assess feasibility of new R&D project. •Authored internal reports for characterization and comparability of manufacturing processes. •Authored and reviewed test protocols and procedures for characterization and analytical test methods. •Process development, optimization and scale-up (g-kg), including protein/peptide conjugation, enzymatic transformation, column purification and UF/DF unit operations. Technical transfer and monitoring of GMP manufacturing of API at external contract site including review of batch records. •Experience working on development of biologics and recombinant protein therapeutics. •Experience in FDA regulated environment and followed GMP and ICH guidelines.
United States
Clayton
Pharmaceuticals
HPLC method develoment and qualification, Capillary Electrophoresis method development and validation, GC-MS and LC-MS analysis, Tangential Flow Filtration, UF/DF and Dialysis, Analytical Method development, qualification and validation, Process Development and Scale-up, Experience in FDA regulated environments; followed GMP and ICH guidelines, FDA, Technology Transfer, GMP, Analytical Chemistry, HPLC, Purification, Process Simulation, Sop, Characterization, Laboratory, Cross-functional Team Leadership, Biopharmaceuticals, R&D
Experience

Validation Engineer
Hospira, A Pfizer Company

Validation Engineer
Assess and document impact and risk associated with process changes. Develop and implement validation strategy to implement changes. Execute process validation activities in accordance with industry standards and approved protocols. Author summary reports of process validation activities.

Quality Engineer
Hospira

Research Scientist - Analytical Development
Grifols Therapeutics
Clayton, NC
Develop methods for analysis of protein purity using HPLC and electrophoresis
Monica Puskas's Contact Information
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