Jocelyn Bailey Email & Phone Number

California, United States

Hercules, Ca, Us

- Developed program and requirements strategy for design and development of 4 parallel reagent assay kit products and software tool; executed to strategy and met timeline via proactive risk identification, agile resource and task allocation, and delving into the details to remove blockers.- Successfully managed 10 new product development projects to commercial launch, delivering all projects in an average of 8-12 months, with an average budget of $2M. Focused on research products in ddPCR, gene expression, and chromatography.- Oversaw agile-driven new product development (SDLC) for cloud-based Digital Assays e-commerce and assay design platform with scrum team of 6-8 members. Defined and prioritized tasks, reviewed release documentation, supported defect triage and risk management, leading the team to deliver 7 full release cycles in 24 months.- Transferred over 100 SKUs to internal or external manufacturing by coordinating cross-functional teams of R&D, Manufacturing, Marketing, and QA in order to ensure product quality and adherence to design control.- Led cross-functional core teams in new product development (NPD) projects from concept / feasibility to manufacturing transfer and global launch, following design control and ISO 13485 medical device design and development principles. Managed and owned 7 NPD projects to completion.

Hercules, Ca, Us

New Product Development in Life Sciences Group- Manages NPD projects in design control and ISO 13485 environment for reagent, instrument and software product development projects- Supports Change Control and CAPA projects affecting LSG R&D

Bethesda, Md, Us

Managed ~15 projects to support 10 clients in fields of flow cytometry, immunogenicity assays (PK, ADA, NAb), routine sample processing supporting Phase 1/2 clinical trials; contract values ranging up to $1M. Primary point of contact for clients at the CRO. Types of projects: flow cytometry assay development; assay development to validation for immunogenicity assays (PK, ADA, NAb); sample testing & routine processing for Phase 1/2 clinical trials, real-time flow cytometry sample testing; delivery of biomarker data through software platform Primary job functions include: executing multi-disciplinary client projects from initiation to completion, maintaining internal and external timelines by working directly with all stakeholders, managing client relationships and client communications, handling financial reporting and scope changes, and solving issues by working with management and technical teams.

Zurich, Zh, Ch

MaxWell Biosystems is an early-stage start-up that spun out of ETH Zurich in late 2015. The company develops highly advanced high-resolution electrophysiology instrumentation to accelerate neuroscience and stem cell research. Roles:- Designed and executed strategic marketing initiatives to market the start-up’s in vitro electrophysiology platform to academic and company labs, including strategic website improvements, targeted advertising, and company updates.- Conceptualized, designed, and published new featured website page, a technology 'landing' page, which serves to visually display the company's innovation and products in a simple manner. - Utilized Atlassian Confluence and JIRA to manage issue tracking and event management for marketing-related tasks.

CellSpring is an early-stage startup that spun out of ETH Zurich in early 2015. The company leverages its “3D Bloom” technology and automation to offer a unique 3D cell culture tool to enhance R&D and preclinical drug testing.Roles:- Managed corporate partnerships and scientific contract projects with 4 external companies, producing deliverables including Application Note, experimental results package, and survey for Early Access to Product.- Developed scripts and tested parameters to implement Tecan Freedom EVO liquid handling automation for seeding cultures and performing cell-based assays on company’s 3D cell culture technology. - Developed and streamlined automation and laboratory workflows for daily and project-based scientific operations, resulting in improved resource utilization, improved consistency, faster turnaround times, and more user friendly operation. - Conceptualized and redesigned website's homepage in Adobe Muse; designed and executed product instruction sheets and product labels . Accomplishments:Certification: TECAN S-7 EvoWare Basics, June 2017Publication: TECAN Application Note, "Screening drug efficacy in 3D," July 2017

Palo Alto, Ca, Us

Assay Development teams worked to publicly verify performance of company’s new generation of assays, blood collection devices, and clinical laboratory diagnostic devices amidst major regulatory challenges. Roles & Responsibilities:- Worked on cross-functional teams to execute high priority projects and to verify assay performance on in vitro diagnostic (IVD) devices; teams included R&D, Assay Development, Systems Integration Engineering, Hardware Engineering, CLIA Clinical Lab, Clinical Studies, Data Analysis, Project ManagementProject Areas:- Assay Development (immunoassay / ELISA development): designed, optimized, developed and validated preclinical immunoassays, according to FDA 510(K) guidelines- Product Development (in vitro diagnostic (IVD) device development): executed studies to demonstrate assay performance on IVD device; conducted data analysis and error troubleshooting; implemented calibration and quality control procedures according to CLSI guidelines - Project Management: improved efficiency, reproducibility and consistency for cross-functional assay development projects; created and oversaw project logistics, resource requirements, and timelines; communicated across teams to align multidisciplinary project efforts - Clinical Studies: standardized in-house clinical study best practices; optimized parameters for blood collection protocols compatible with CLIA regulation- Software & Data Analysis: Microsoft Project, Microsoft Access, Agile PLM, R-Script, Analyze-It

South San Francisco, California, Us

- Act as liaisons between Genentech and UCLA to represent Genentech, share resources, and host events and infosessions for potential UCLA applicants. Activities as Ambassador: - Hosted weekly office hours for students, coordinated with company reps to host infosessions and webinars, and helped students revise their resumes in one-on-one resume sessions- Events: weekly office hours, Meet & Greet, resume webex workshop, one-on-one resume review office hours, Genentech infosession & science talk, cohosted Genentech recruiting infosessions

South San Francisco, California, Us

Technical Areas:Biomarker development, histology, immunohistochemistry (IHC), in situ hybridization (ISH), Ventana, Dako and Tecan automated platforms, oncology, immunology, antibody drug conjugatesResponsibilities:- Developed highly specific RNA and immunostaining (IHC and ISH) protocols on automated Ventana and Dako platforms in order to investigate targeted biomarker expression in clinical oncology samples. Achievements:- Delivered and presented results (evaluation of biomarker for predictive and diagnostic use on lung cancer clinical samples) in poster and oral presentation to 50 members of Pathology department. - Spearheaded, created, and moderated "Genentech Interns 2014" Facebook group to improve networking amongst interns. Communicated and aligned efforts with Genentech College Programs Team.

Biomaterials and Tissue Engineering Laboratory, Dr. Andrea Kasko"Saccharides as a viable alternative to peptides in mediating cell adhesion"- Characterized and evaluated cell viability on novel polysaccharide hydrogels using molecular biology techniques- Synthesized, purified, and characterized engineered polymer chains, using organic chemistry techniques such as extraction, column chromatography, thin layer chromatography, NMR

Zürich, Ch

Cartilage Engineering + Regeneration Laboratory, Dr. Marcy Zenobi-Wong"Novel systems for bioadhesion in cartilage tissue engineering" - Characterized cartilage stem cell microtissues using standard cellular biology techniques, including RT-qPCR, in situ immunostaining, cryosectioning and histology, confocal fluorescence microscopy