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 decision-making within the team, and coach colleagues on standard methodologies for negotiation and problem-solving. Work closely with the customer to advocate their program in both internal and external conversations. Track and manage the financial aspects of the project including milestone payments, pass-through costs, and labor estimates to ensure that we adhere to schedule and are on budget.

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 my Korean national counterparts. Lead multiple interdisciplinary project teams to develop and deliver the operational strategy to meet client and company objectives in a contract biopharmaceutical manufacturing environment. Enhance cross-functional team performance using negotiation, facilitation, risk management, and conflict resolution skills. Create and execute program level work strategies, timelines, resource assessments, risk assessments, mitigation strategies, scenario planning, and cost estimates for implementation in the site’s cGMP production facilities. Provide leadership to PM staff with coaching, training, skill development opportunities, constructive feedback on performance and progress toward goals and expectations.

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 production (aseptic and packaging) facilities. Create and execute program-level project work strategies, timelines, resource assessments, risk assessments, mitigation strategies, scenario planning, and cost estimates for implementation. Provide project management guidance and leadership to technical project managers. Review deliverables prepared by team to ensure alignment with standardized PM process work stream and stakeholder expectations. Provide timely and accurate invoicing, and monitor receivables to track project/program costs.

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 training, address questions, resolve issues and monitor the production process for new drug products and components. Create and execute project work plans, timelines, and cost estimates for project implementation. Effectively apply operating processes and project management tools to verify project standards are met. Ensure project documents are complete, current, and stored appropriately. Track and report team hours and expenses.

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 variances to expected performance, results and alerting senior management to inter-departmental issues or conflicts in meeting production and quality objectives. Work with cross-functional teams to identify and implement continuous improvement efforts.

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 fermentation and tissue culture bioreactors for the production of biotherapeutics. Develop internal capacity for the production of technology platforms that can be used to enhance the quality of the client’s product.

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 how they will meet the needs of our customers. Design and implement the strategic goals and objectives of the organization. Provide direction and leadership toward the achievement of the organization's philosophy, mission, strategy, and milestones.

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 enzymes for accurate identification of positive control reactions. Work with automated liquid handlers: Tecan (Genesis and EVO) and Beckman (2000 and FX.)

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 criteria prior to transplant. Purchase inventory under a JIT model. Maintain accurate records of all purchases for lab and clinical program. Update and create protocols for the lab. Measure metabolic charge ratios using HPLC. Extract and quantify DNA from cell samples. Measure islet insulin production using ELISA to determine functionality. Maintain proper laboratory notebook and paperwork for the lab.

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 network including Novell, Appletalk, Unix, and NT/2000. Create user accounts, troubleshoot account problems, maintain and transfer accounts between machines.

M.S. In Biotechnology

B.S. In Biological Science

B.A. In Studio Art