Eric Hatch Email & Phone Number

Edwardsville, IL, US

Paris, France, FR

Waltham, MA, US

Demonstrate leadership in the execution of drug substance programs within the St. Louis production facility. Plan and deliver client milestones through all stages of the project including process development, analytical development, technology transfer, and new product introduction into cGMP manufacturing. Resolve project team issues, facilitate.

Waltham, MA, US

Yeonsu-gu, Incheon, KR

Successfully managed a large commercial program portfolio for the aseptic production of small molecule and biologic drug product vials. Smoothly overcame the challenge of working overseas in a bilingual environment, working with a global client portfolio, and navigating international business practices through collaboration and relationship building with.

New York, New York, US

Manage program level life-cycle maintenance and development objectives related to the auto-injector delivery system, parenteral drug treatment, and combination medical device product. Identify needed resources and recruit or assign individual responsibilities for the development of new products and new processes to be implemented in the site’s cGMP.

New York, New York, US

Manage day-to-day operational aspects of project and scope for department objectives. Maintain aseptic gowning qualification status to be able to monitor the production of new products in the sterile production facility. Employ device design controls to monitor the development and change control process for the auto-injector delivery system. Provide.

Marcy-l'Étoile, Auvergne-Rhône-Alpes, FR

Schedule, supervise and monitor the daily activities of the Receiving and In-Process Quality Control department personnel to ensure that quality attributes are appropriately assessed for all incoming chemicals, incoming materials, semi-finished goods, kit inspection and production auditing. Provide status and progress reports senior management identifying.

Mt Claremont, Western Australia, AU

Manage internal and client projects in the development of novel cell therapy biopharmaceutical agents for phase I/II clinical trials. Work with clients to ensure proper tech transfer of their product, scale up, production schedules, master batch record creation, quality control specification design, and provide information on cGMP and FDA regulations. Run.

Identify and develop new business leads through a coordinated outreach. Conduct marketing research on competitive products and create SWOT analysis to help guide and define marketing objectives. Write product development and marketing plans. Establish and maintain customer relationships by focusing on what our products do better than the competition and.

US

Manufacture synthetic DNA fragments (oligonucleotides) purified by HPLC and used for FRET based detection of single nucleotide polymorphisms while following cGMP regulations for invitro diagnostics. Formulate media and components for standard and specialized products. Perform gel electrophoresis on plasmid preparations of DNA digested with restriction.

Follow SOP’s under a cGMP setting to isolate islets of langerhans from donor pancreata for an IND transplantation program. Prepare media using aseptic technique in an ISO class 7 cleanroom. Culture Islets, HB124(Insulin anti-body producing Hybridoma), and INS-1(rat insulinoma cell line) cells. Perform LAL(Endotoxin) test of the final product as a release.

Provide technical writing services incorporating scientific data into technical reports to support environmental consulting contracts.

Tallahassee, FL, US

Provide phone support for common computer applications to FSU students, faculty, and staff. Issue tickets for field technicians to fix problems not addressable over the phone or via proxy. Develop and support interactive web pages to give information to FSU’s students, faculty, and staff. Maintain, manage, and troubleshoot various servers across the FSU.

M.S. In Biotechnology

B.S. In Biological Science

B.A. In Studio Art