Eric Hatch

Eric Hatch Email and Phone Number

Manager, Program Management @ Thermo Fisher Scientific
Edwardsville, IL, US
Eric Hatch's Location
Edwardsville, Illinois, United States, United States
Eric Hatch's Contact Details
About Eric Hatch

With over 18+ years of experience in the biopharmaceutical industry, I am a seasoned and certified project management professional who is passionate about delivering high-quality therapeutic products that improve the lives of patients. I currently lead a team of six program managers at Thermo Fisher Scientific, one of the world's leading contract development and manufacturing organizations.In my role, I demonstrate leadership, people development, and business strategy skills to execute drug substance programs within the St. Louis production facility. I plan and deliver client milestones through all stages of the project, from process development and technology transfer to new product introduction and cGMP manufacturing. I also work closely with the customer to advocate their program and resolve any issues or conflicts that may arise. Additionally, I track and manage the financial aspects of the project, ensuring that we meet the budget and revenue targets. I have successfully managed a large commercial program portfolio for the aseptic production of small molecule and biologic drug product vials, working with a global client base and overcoming the challenges of working in a bilingual and multicultural environment.

Eric Hatch's Current Company Details
Thermo Fisher Scientific

Thermo Fisher Scientific

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Manager, Program Management
Edwardsville, IL, US
Website:
thermofisher.com
Employees:
99360
Eric Hatch Work Experience Details
  • Thermo Fisher Scientific
    Manager, Program Management
    Thermo Fisher Scientific
    Edwardsville, Il, Us
  • Curium Pharma
    Principal Project Manager
    Curium Pharma Dec 2024 - Present
    Paris, France, Fr
  • Thermo Fisher Scientific
    Manager, Program Management
    Thermo Fisher Scientific May 2022 - Sep 2024
    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.
  • Thermo Fisher Scientific
    Staff Program Manager
    Thermo Fisher Scientific Jul 2021 - May 2022
    Waltham, Ma, Us
  • Samsung Biologics
    Senior Manager, Commercial Program Management
    Samsung Biologics Jul 2018 - Jun 2021
    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.
  • Pfizer
    Project Manager
    Pfizer Mar 2016 - Jun 2018
    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.
  • Pfizer
    Technical Project Manager
    Pfizer Aug 2011 - Mar 2016
    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.
  • Biomerieux
    Incoming Qc Group Lead
    Biomerieux Jan 2010 - Jul 2011
    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.
  • Waisman Clinical Biomanufacturing Facility
    Project Manager, Sr. Research Specialist
    Waisman Clinical Biomanufacturing Facility Jul 2006 - Dec 2009
    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.
  • Integrazyme, Llc
    Managing Member
    Integrazyme, Llc Mar 2006 - Jan 2009
    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.
  • Third Wave Technologies
    Manufacturing Technician
    Third Wave Technologies Jan 2006 - Jul 2006
    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.)
  • Uw-Madison Medical School Dept. Of Surgery
    Project Manager, Research Specialist
    Uw-Madison Medical School Dept. Of Surgery Mar 2004 - Jan 2006
    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.
  • Delta Seven Environmental Consulting
    Associate Biologist
    Delta Seven Environmental Consulting Dec 2002 - Feb 2004
    Provide technical writing services incorporating scientific data into technical reports to support environmental consulting contracts.
  • Florida State University
    Computer Support Specialist
    Florida State University Jul 1999 - Apr 2002
    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.

Eric Hatch Skills

Biotechnology Gmp Pharmaceutical Industry Cross Functional Team Leadership Fda Quality Assurance Project Management U.s. Food And Drug Administration Medical Devices Validation Lifesciences Hplc Molecular Biology Sop R&d Six Sigma Capa Data Analysis Cell Culture Cell Laboratory Change Control Statistics Life Sciences Management Process Improvement High Performance Liquid Chromatography Business Process Improvement Assay Development Software Documentation Elisa Purification Corrective And Preventive Action Standard Operating Procedure Research And Development

Eric Hatch Education Details

  • University Of Wisconsin-Madison
    University Of Wisconsin-Madison
    M.S. In Biotechnology
  • Florida State University
    Florida State University
    B.S. In Biological Science
  • Florida State University
    Florida State University
    B.A. In Studio Art

Frequently Asked Questions about Eric Hatch

What company does Eric Hatch work for?

Eric Hatch works for Thermo Fisher Scientific

What is Eric Hatch's role at the current company?

Eric Hatch's current role is Manager, Program Management.

What is Eric Hatch's email address?

Eric Hatch's email address is ew****@****ail.com

What is Eric Hatch's direct phone number?

Eric Hatch's direct phone number is +121257*****

What schools did Eric Hatch attend?

Eric Hatch attended University Of Wisconsin-Madison, Florida State University, Florida State University.

What are some of Eric Hatch's interests?

Eric Hatch has interest in Economic Empowerment, Environment, Science And Technology, Arts And Culture, Health.

What skills is Eric Hatch known for?

Eric Hatch has skills like Biotechnology, Gmp, Pharmaceutical Industry, Cross Functional Team Leadership, Fda, Quality Assurance, Project Management, U.s. Food And Drug Administration, Medical Devices, Validation, Lifesciences, Hplc.

Who are Eric Hatch's colleagues?

Eric Hatch's colleagues are Germina Rosenova, Vincent Curtin, Huiqiong Fan, Neeraj Shetty, Carly Norris, Zeynep Özcan, Phd, Barbara Fehér.

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