Mark Doring

Mark Doring Email and Phone Number

Project Manager and Sr. Application Consultant @ Cenevo (Formerly Labguru & Titian Software)
New Jersey, United States
Mark Doring's Location
Hillsborough, New Jersey, United States, United States
Mark Doring's Contact Details

Mark Doring personal email

n/a

Mark Doring phone numbers

About Mark Doring

Lead Scientist and lab manager with extensive experience in HTS automated operations, liquid handling, and robotic technologies with a proven track record of success. Expertise in biochemical assay development, analytical data review, screening, and in the evaluation, design, integration, and trouble-shooting of automated laboratory systems. Disciplined, dependable and hardworking driven to promote good relationships with internal and external clients and vendors.Specialties: • Lab Automation for Liquid Handling, Microplate Handling and Compound Management • Instrumentation Integration,Troubleshooting, Repair • Assay Development, and High Throughput Screening • Sample Preparation Methods and Techniques • Evaluation and development of IT tools for sample tracking and biochemical data analysis • Small and large scale project management. • Process workflow analysis, design and optimization. • Knowledge in the fabrication processes of automated instrumentation, instrumentation, and labware.

Mark Doring's Current Company Details
Cenevo (Formerly Labguru & Titian Software)

Cenevo (Formerly Labguru & Titian Software)

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Project Manager and Sr. Application Consultant
New Jersey, United States
Website:
cenevo.com
Employees:
109
Mark Doring Work Experience Details
  • Cenevo (Formerly Labguru & Titian Software)
    Project Manager And Sr. Application Consultant
    Cenevo (Formerly Labguru & Titian Software)
    New Jersey, United States
  • Titian Software
    Project Manager / Sr. Application Consultant
    Titian Software Mar 2015 - Present
    London, Gb
    Titian's Mosaic software is the leading laboratory sample management software solution for life science laboratories. My consultant role here involves collaborative Project Management with Pharma and Biotech clients to customize the Titian suite of Mosaic software products to their individual sample management needs. This includes:• In-depth analysis and documentation of laboratory procedures to accurately capture client requirements• Initiating development projects as necessary to provide new or augmented functionality• Working with programming staff to follow through on system configuration• Using my laboratory experience to test the system to ensure that the configuration meets the needs of the client• End-user training• Coordination of deployment and UAT involving the laboratory staff and instrumentation • Final acceptance and hyper-care after the system is moved into Production
  • Resultworks, Llc
    Senior Consultant
    Resultworks, Llc Apr 2013 - Dec 2014
    A professional services consulting company, ResultWorks specializes in transforming the business strategies of Life Sciences companies into successful technology and process harmonization initiatives.The work entailed performance of in-depth analysis of laboratory procedures and processes to accurately capture client efficiencies, pain points, gaps and new requirements. The reports generated were to enable the client (mostly Big Pharma) to make informed decisions on where they needed to focus their efforts, as well as to suggest the best solutions for meeting their requirements based on budgetary and technical data. Summary findings were presented to upper management using easy to understand tables, diagrams and animation tools.
  • Professional Training
    Lab Automation And It
    Professional Training Jul 2012 - Mar 2013
    PMI certified coursework in project management.
  • Merck Research Laboratories, In Vitro Pharmacology, Automation & It
    Sr. Principal Scientist
    Merck Research Laboratories, In Vitro Pharmacology, Automation & It Nov 2010 - Jun 2012
    Rahway, New Jersey, Us
    Lead identification and optimization support of medicinal chemistry and pre-clinical discovery efforts through application of lab automation and IT tools within a secondary screening group. Responsible for a group of automation and IT scientists to develop and validate liquid and materials handling procedures in support of dose-dependant compound testing. Assay validation performed in accordance with published NIH guidelines. • Informatic support included SQL updates and maintenance of a database that linked to a SharePoint TeamSite, and specification and development of custom software products for compound management operations. • Discovery and evaluation of new technologies (instruments, software tools) to increase data quality and integrity and reduce manual efforts. • Initiated and managed vendor negotiations to upgrade and maintain laboratory instrumentation, while saving Merck more than $60K through securing various discounts. • Coordinated presentations by vendor experts in promulgating the proper use of their technologies to drive results and manage expectations.
  • Schering-Plough Research Institute, New Lead Discovery
    Principal Scientist, Automation Group Lead
    Schering-Plough Research Institute, New Lead Discovery Apr 1985 - Nov 2010
    Kenilworth, New Jersey, Us
    Held positions of increasing scientific and managerial responsibility that enabled me to contribute significantly to meeting or exceeding High Throughput Screening (HTS, uHTS) departmental goals. * Our screening goals increased yearly to culminate with the successful evaluation of approximately 2 million chemical entities through a battery of 20 – 30 novel biochemical and cellular assays each year* I played a key role in bringing in new technological improvements to transition screening from test tubes to 96 to 384 to 1536-well formats* I’ve evaluated talent since early in my career and built and managed teams of up to 13 FTE’s in support of biochemical and cell-based screening. I have used many methods and tools for personnel assessment, and have supervised temporary, part-time, contract and full-time employees• Liquid handling methods programmingTransition of assays from the bench to automated platforms by working closely with bench scientists, and developing specific reagent handling methods• Application of Project Management techniques to determine appropriate process and automation needs• Assay development and performanceCharacterization and execution of a wide variety of in vitro assays, statistical review of data and report generation• Compound management for various sample sets (Natural Products, CombiChem, Synthetics)Sample acquisition, storage, prep, and formatting. Method development for mixture creation(orthogonal, etc.), hit picking, and rearray to meet assay needs• IT development and supportProgramming (liquid handling, microplate processing, supervisory scheduling software, etc.)• Management of vendor interactions to specify systems, critically review products, instruct staff and resolve issues• Management of interactions with site facilities staffWorked as a department rep and key decision maker for a wide variety of facilities projects.Work with SPRI R&D engineering to design and build peripherals specific to our needs
  • Schering-Plough Research Institute, New Lead Discovery
    Associate Scientist
    Schering-Plough Research Institute, New Lead Discovery Nov 1986 - Jan 1992
    Kenilworth, New Jersey, Us
    Supervision of three BS level scientists in the development, optimization and performance of a wide variety of in vitro biochemical assays using radioisotopic and colorimetric tracers. Assay types included ELISA, enzyme inhibition, and receptor binding assays. Biochemical techniques included: determination of enzyme kinetics, characterization of receptor binding systems, enzyme and receptor isolation and preparation, protein purification through affinity chromatography, radioligand synthesis and purification, tissue culture of mammalian carcinoma cell lines, and small animal handling. Coordinated testing of unique structure compound files through all biochemical and microbiological assays running at the Bloomfield facility. Data analysis and reporting was handled using RS/1 software. Created custom software products for data analysis by programming using RPL.Developed automated liquid handling procedures (using Tecan robotics) for natural product sample preparation, and for biochemical assay performance. Developed various specialized protocols to facilitate labor-intensive assay steps: organic phase separation for a cholesterol transferase assay (ACAT), anion chromatography for the HIV reverse transcriptase, and homogeneous, temperature controlled cell suspension additions for phospholipase assays.Assisted in the design and integration of a gantry robotic system for the automation of sample preparation and sample transfer procedures. Provided all automated liquid handling code, and collaborated closely with Schering’s R&D engineering staff for fabrication and modification of various custom components.
  • Schering-Plough Research Institute, New Lead Discovery
    Assistant Scientist Ii
    Schering-Plough Research Institute, New Lead Discovery Apr 1985 - Nov 1986
    Kenilworth, New Jersey, Us
    Performance and troubleshooting of established HPLC separation procedures for the detection of antifungal agents (everninomycin and ketoconazole). Development of solid phase extraction techniques for serum samples. Independent design of in vitro experimental protocols by adapting techniques obtained from the existing literature (myosin light chain kinase, phosphodiesterase type I). In addition, I performed quality control (RIA) on α-interferon samples, and biochemical screening of fermentation products and plant extracts for possible cell wall (chitin, glucan) synthetase inhibitors.
  • Sgs
    Wet Chemist
    Sgs Apr 1984 - Apr 1985
    Geneva, Geneva, Ch
    AA, GC, and UV/VIS spectroscopic analysis of agricultural and petroleum products performed as a service to outside clientele. Quality control services following ASTM procedures included:• Wet chemical analysis of reagents, petrochemicals and petroleum distillates.• Gasoline octane rating and residual fuel oil analysis.• Moisture and fat content determinations of agricultural products.• Recommendation of cargo acceptance according to industrial specifications.Assignments also included performance of job responsibilities on second shift, and 24-hour on-call service on an alternating schedule.

Mark Doring Skills

High Throughput Screening Assay Development Laboratory Automation Drug Discovery Biotechnology Biochemistry Pharmaceutical Industry Lifesciences Lims Automation R&d Elisa In Vitro Project Management Leadership Compound Management Enzyme Kinetics Uv/vis Cell Culture Problem Solving Gpcrs User Acceptance Testing Asset Managment Asset Management

Mark Doring Education Details

  • Seton Hall University
    Seton Hall University
    Biology
  • Upsala College
    Upsala College
    Biochemistry
  • Glen Ridge High School
    Glen Ridge High School

Frequently Asked Questions about Mark Doring

What company does Mark Doring work for?

Mark Doring works for Cenevo (Formerly Labguru & Titian Software)

What is Mark Doring's role at the current company?

Mark Doring's current role is Project Manager and Sr. Application Consultant.

What is Mark Doring's email address?

Mark Doring's email address is mw****@****ast.net

What is Mark Doring's direct phone number?

Mark Doring's direct phone number is (610) 768*****

What schools did Mark Doring attend?

Mark Doring attended Seton Hall University, Upsala College, Glen Ridge High School.

What are some of Mark Doring's interests?

Mark Doring has interest in Children.

What skills is Mark Doring known for?

Mark Doring has skills like High Throughput Screening, Assay Development, Laboratory Automation, Drug Discovery, Biotechnology, Biochemistry, Pharmaceutical Industry, Lifesciences, Lims, Automation, R&d, Elisa.

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