Greg Furrow, M.S., Frqa Email & Phone Number

Boston, MA, US

Worcester, Massachusetts, US

Worcester, Massachusetts, US

Worcester, Massachusetts, US

Responsible for Manufacturing Science and Technology, Preclinical Sciences (Process Development, Analytical Development and Translational Science), CMC Development, Quality Assurance, Quality Control Laboratories, Operations and Facilities.

Worcester, Massachusetts, US

Worcester, Massachusetts, US

Directly responsible for leading the Quality Organization inclusive of Clinical Quality Assurance, Manufacturing Quality Assurance, Quality Control Chemistry, Microbiology, and Raw Material, and Quality Systems in compliance with Food and Drug Administration (FDA) current Good Manufacturing Practices (cGMP), Good Clinical Practices (GCP), Good Laboratory.

Birmingham, Alabama, US

• Key Focus:
• Lead Quality and Compliance, Bio Safety, ISO 9000, Human Resources, IT, EH&S, and Export Control for this 501(c)(3) nonprofit, scientific research organization with ~500 scientists and engineers working with the.
• Serve as the Institutional Official for Biosafety and IACUC
• Focus on accelerating data quality improvement, enhancing good documentation practices procedures and training, as well as implementing enhanced safety procedures
• Perform compliance, consulting, training and audits for clientsKey Results:
• Developed and executed key metrics to monitor and improve quality and compliance (IT, HR, Bio Safety, EH&S)

West Lafayette, IN, US

Experienced executive with proven skills in FDA, OECD and EPA regulatory compliance, environmental health and safety compliance, executive management, quality improvement, personnel development and coaching, metric development, team building, and strategic planning.

• Key Focus:
• Recruited by CEO to unify a decentralized quality organization and to enhance and harmonize compliance procedures globally for this large company employing 1400 scientists, technicians and support staff across US /.
• Provided Quality and Compliance oversight for product safety, toxicological research, bioanalytical, regulatory compliance, formulation and manufacturing services for pharmaceutical, biotechnology, industrial and.
• As member of Executive team, drove revenue CAGR of 11% and adjusted EBITDA CAGR of 13%, which led to a successful exit strategy in early 2016 to Charles River for $585M (12.9x TTM EBITDA)
• As member of Executive team, increased enterprise value by 144% generating a 50% IRR for investors
• Performed QA and EH&S due diligence of Ricerca Biosciences’ Lyon, France business resulting in acquisition by WIL; the Lyon site = 16x ROI within three years

Charlottesville, Virginia, US

Wilmington, Massachusetts, US

• Key Focus:
• Directed Regulatory Affairs and Compliance for company providing essential products and services to accelerate client research and drug development efforts, including: o Global Pharmaceutical, biotechnology, government.
• Served as GLP QA Lead for a major sponsor’s internal GLP improvement effort
• Led QA oversight of construction, validation and creation of compliance oversight program for Charles River’s Shrewsbury site and led GLP QA functional groups at Wilmington, Worcester, Shrewsbury and all Pathology.
• Led successful on-time validation and start-up of Charles River’s best-in-class facility in Shrewsbury MA.
• Decommissioned the Charles River Worcester MA site

Indianapolis, Indiana, US

• Key Focus:
• Managed Research Quality Assurance oversight (GLP, GCP)
• Other roles included: Human Resources Account Manager, Department Head for Quality Control and Analytical Services (cGMP), Productivity Projects Facilitator, Analytical ChemistKey Results:
• Integrated Elanco Animal Health and Lilly Pharmaceutical QA units (synergy/reduced QA headcount)
• Led quality improvement effort and revamped the quality systems at the Lilly Phase I clinic which culminated in an FDA inspection with no 483 issued; (no adverse findings)
• Co-created good research practices policies for Discovery Research / QA oversight

Washington, DC, US

Key Skills and Expertise:#LeanSixSigma#ProcessImprovement#ProgramManagement#ProjectManagment#QualityAssurance#RegulatoryCompliance#TQM#ConsultantGLPGCPcGMPComputerized System ValidationSix SigmaQuality ImprovementMentoringPersonnel developmentCoachingLeadershipExecutive managementDrug DevelopmentQuality ConsultingRegulatory trainingGlobal RegulationsOECD.

Bs, Ms, Analytical Chemistry

Education record

Education record