Developing, validating and optimizing bioassays and automation initiatives for preclinical, clinical, and product release studies in collaboration with clients and cross-functional teams is what I do best.

Leadership capabilities, technical skills and performance highlights transferable to your organization include:

à 15+ years biopharmaceutical industry experience managing bioassay development and automation programs, working closely with customers and providing team leadership and end-user training to ensure successful on-time execution of assays, troubleshooting, validation and sample testing under GxPs.

à Laboratory experience includes leading and collaborating with cross-functional teams in mammalian cell culture and cell-based assay development and validation; extensively designed and executed experiments, conducted statistical analysis and presented data internally and externally.

à Established innovative laboratory automation initiatives that resulted in integrated electronic workflows, and harmonization of bioassay performance across three sites, Cambridge, RTP, and San Diego.

à Traveled extensively across the USA to meet with clients and I am currently opened to travel more than 50% of the time to support customers’ needs and achieve company objectives under time constraints.

à Published technical application notes for various companies including Cellomics and Invitrogen, demonstrating automation of cell-based and nucleic acid purification methods using integrated Beckman Coulter and Tecan liquid handling systems; presented on automated assay workflows and 21 CFR Part 11 compliance at the 2004 AAPS conference in Baltimore, MD.

à Possess MBS and MA degrees in biological sciences, a broad bioanalytical background, commercial acumen and determination to consistently deliver value to meet customer needs.