•Company program development including scientific/clinical literature review, summarizing and presenting key information to diverse parties, market/regulatory research, strategy development, discussions with key opinion leaders and decision making•Function as internal knowledge expert on key programs•Authoring of documents including clinical study protocols, conference presentations, regulatory and other documents pertinent to company activities•Vendor and relationship management including CROs, consultants, and clinical trial sites•Intellectual property portfolio management including budgeting, strategy, research and prosecution•Grant funding management•Quality system development and management•Construction of marketing materials and corporate communications•Identifying and outreach to collaborative and funding opportunities

• Project Leader on Company hardware/software endeavours• Lead on product development activities• Vendor management• Conduct market and regulatory research and present findings• Prepare and oversee release of company hardware/software• Responsible for authoring, review, and release of Company documents and records• Formulation and revision of Company policies.• Liaise with executives, employees, vendors, lawyers, and outside groups.• Wrote and managed grant submissions• SOP and process development• Managed operational processes including purchasing, receiving, inspection, and inventory.

• Conducted internal audits of Company processes • Conducted post market surveillance• Reviewed, revised, and maintained Quality Assurance documentation• Provided insight to improve processes and practices to optimize efficiency such as SOP revisions• Ensured documentation is accurate and up-to-date• Monitored and provided guidance to personnel• Reviewed quality and safety regulations to ensure company processes comply

As a consultant to a growing biotechnology Company, I worked closely with executives in advising on key strategic issues and Company objectives. I spearheaded multiple Company projects and managed day to day activities. I managed issues pertaining to IP, regulatory, quality systems, manufacturing, and operations while acting as a Company liaison with external partners/vendors.

I strategically planned and managed multiple Company initiatives. This included managing the Company's IP portfolio, leading regulatory clearance endeavors, overseeing aspects of the quality management system, and various operational activities under the Director of Operations. I also conducted Company pertinent research, liaison activities, and contract review. As the sole internal scientific resource, I provided scientific knowledge and market research data supporting product development, regulatory affairs, and commercialization activities.

I worked on characterization of a somatic stem cell fraction found in adipose tissue and various stem cell-related projects. This included harvesting adipose tissue from rats, culturing of stem cells, differentiation techniques, characterization techniques, and radio assays. I monitored, stocked, and ensured complacency of multiple Lvl 2 government laboratories, as well as training other individuals.Additionally, I wrote/reviewed manuscripts as well as presented findings both internally and externally at major conferences.

I managed and directed of a small staff of employees in all aspects of production and quality monitoring of product, helping to design and implement production protocols to continuously improve efficiency of production.

Responsible for conducting lab sessions for undergraduate students. This included duties such as explaining the principals of all experiments conducted, demonstrating proper techniques, supervising large groups of students, answering any questions presented, and marking lab reports.

Certified trainer responsible for working with others to improve their abilities.Occasionally in-charge of managing all aspects of the establishment’s back-end including the employees