Todd R. Daviau Email & Phone Number

North Brunswick, NJ, US

Boston, Massachusetts, US

Support the Growth of MassChallenge Healthcare & Texas Ecosystem: Play a key advisory role in shaping and expanding MassChallenge’s healthcare initiatives, with a particular focus on the Texas ecosystem.Advise Startups: Provide expert guidance, mentorship, and strategic advice to startups within the healthcare and biotechnology sectors, helping them.

Texarkana, Texas, US

• Led by investor group; Signet Healthcare & GMS Capital, assuming operations of HUMCO, leading consumer goods, first aid, and personal care CDMO.
• Provided visionary leadership, strategic planning, and financial management as CEO to drive the company's growth and success.

Texarkana, Texas, US

• Made critical corporate decisions, drove business development, and oversaw financial management in collaboration with the Board of Directors to set strategic goals, establish business priorities, and identify growth.
• Worked with the Business Development team to build strategic partnerships and foster strong relationships with key stakeholders; led the executive team to ensure regulatory compliance, monitor industry trends, manage.
• Drove innovation and continuous improvement within the organization, turning a -$5.5M EBITDA into a +$0.25M EBITDA in under 2 years,
• Lead development of product projected to generate over $12M in sales in 2023; increased top-line revenues by over 25% in one year and created a Product Development team, streamlining operations with new equipment and.

Tampa, Florida, US

Appointment as Assistant Professor for the Inaugural Class in the New USF College of Pharmacy.

Tampa, Florida, US

• Served on the Founding Board of Advisors for the University of South Florida's College of Pharmacy.
• Contributed to the establishment of educational standards that distinguish the USF College of Pharmacy in pharmaceutical education.
• Advocated for the development of Master of Science (M.S.) and Doctor of Philosophy (Ph.D.) programs in industrial pharmaceutics.
• Collaborated with the USF College of Business to initiate a joint MBA/PharmD program focused on Biotech Entrepreneurship.

Clearwater, FL, US

CoreRx is a full-service pharmaceutical contract development/manufacturing organization (CDMO) dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate obstacles in order to bring new drugs to market, and more importantly, to the people who need them most. We have a proven track record and extensive expertise.

Clearwater, FL, US

King Of Prussia, Pennsylvania, US

• Focused on fostering innovative and cutting-edge methodologies, optimizing resource utilization, and adhering to strategic organizational objectives.
• Provided leadership and direction to a 22-member Analytical Chemistry team, ensuring alignment with departmental and corporate goals.
• Developed and executed strategic plans for the Analytical Chemistry group, synchronizing departmental functions with company-wide targets.
• Managed the group's financial operations, including budgeting, resource allocation, and cost containment, to maintain fiscal responsibility.
• Executed strategic decisions regarding analytical methods, processes, and technological advancements to enhance operational efficiency.
• Drove business development efforts, enhancing client engagement and satisfaction and spearheading the acquisition of new business ventures.

Columbia, MD, US

• Provided robust support to the sales team, enabling them to present and sell our comprehensive instrument line effectively.
• Conducted in-depth customer training sessions for various instruments, including software, UV-Vis spectrophotometers, FTIR, HPLC, GC, GC-MS, LC-MS, TOC analyzers, and thermal analysis equipment, ensuring clients are.
• Performed dynamic equipment and software demonstrations, showcasing the capabilities and benefits of our products to potential customers, thereby aiding in the sales process and customer engagement.

• Managed the Analytical laboratory for a line of polyamine products initially discovered at the University of Florida, ensuring efficient operation and accurate results in product testing and analysis.
• Was responsible for preparing and maintaining comprehensive documentation, specifically the Chemistry, Manufacturing, and Controls (CMC) sections that are essential for Regulatory filings, including Investigational New.

US

• Developed, validated, and performed sample analyses of bulk drugs, raw materials, and finished product dosage forms, utilizing techniques such as Gas Chromatography (GC/GC-MS), Gel Permeation Chromatography (GPC), and.
• Prepared and managed essential documents supporting Investigational New Drug (IND) and New Drug Application (NDA) submissions, contributing to the company's regulatory approval process.

• Responsible for establishing and maintaining wholesale accounts with firms specializing in specialty chemicals (additives and test kits) and electronic devices for public and private aquariums.
• Accountable for training wholesale sales representatives.
• Conduct informal discussions on testing, chemicals, and their uses at top-performing retail accounts.

• Tasked with the development and validation of analytical methods.
• Conduct sample analysis of bulk drugs, raw materials, and finished product dosage forms using GC, CE, and HPLC techniques.
• Act as Chromatography System Manager, overseeing daily operations, training, and validation of the DEC Microvax II and analytical instrumentation.
• Selected as Beta test site System Manager by Beckman Instruments for versions 2.0, 2.1, and 2.2 of their PeakProTM Chromatography Software.

Washington, DC, US

Petty Officer, Port Security, Law Enforcement

• Developed and validated analytical methods for drugs and their metabolites for use in pharmacokinetic studies.
• Founded and managed the operations of a cGMP in-vitro drug testing laboratory within a Contract Research Organization (CRO), aimed at generating contract revenue.
• Headed the drug stability and dissolution group, overseeing the testing and release of client stability samples.
• Planned and structured the departmental organization, including the setup of the laboratory and its equipment; also responsible for reviewing/approving laboratory data, reports, and SOPs.
• Played a key role in recruiting and training laboratory staff.
• Evaluated and improved stability/analytical testing, methods development, and validation programs across various product types.

• Formulated specifications for raw materials, dosage forms, and packaging materials.
• Established Standard Operating Procedures (SOPs) for the testing and release of drug substances, excipients, and preservatives.
• Developed and validated analytical methods to aid new product development and regulatory submissions, specifically for generic parenteral products.
• Accountable for preparing analytical and stability documentation for Abbreviated New Drug Applications (ANDAs).

Master Of Business Administration (M.B.A.), Business, Management, Marketing, And Related Support Services

Bachelor Of Science - Bs, Chemistry/Marine Biology