Chris Barringer (Mba, Pmp)

Chris Barringer (Mba, Pmp) Email and Phone Number

Quality Engineer, Program Manager @ FUJIFILM Biotechnologies
United States
Chris Barringer (Mba, Pmp)'s Location
High Point, North Carolina, United States, United States
Chris Barringer (Mba, Pmp)'s Contact Details

Chris Barringer (Mba, Pmp) personal email

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Chris Barringer (Mba, Pmp) phone numbers

About Chris Barringer (Mba, Pmp)

Highly experienced and certified scientific project manager (principle investigator) with a diverse portfolio of interest, abilities, and experience devoted to the development and application of new technologies, products, and services. Unique combination of technical knowledge and managerial skills dedicated to the completion of complex and innovative projects as scheduled, on budget, and according to quality specifications. Expert in building relationships and managing communication across a diverse range of stakeholders. Lifelong learner who enhanced scientific career by earning a MBA in BioSciences Management and certification as a PMP professional.

Chris Barringer (Mba, Pmp)'s Current Company Details
FUJIFILM Biotechnologies

Fujifilm Biotechnologies

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Quality Engineer, Program Manager
United States
Chris Barringer (Mba, Pmp) Work Experience Details
  • Fujifilm Biotechnologies
    Quality Engineer, Program Manager
    Fujifilm Biotechnologies
    United States
  • Thermo Fisher Scientific
    Program Manager, Bio Division
    Thermo Fisher Scientific Nov 2020 - Present
    Waltham, Ma, Us
    Global Program Manager focused on developing biological Drug Substance manufacturing and operations for NCE’s, including process establishment, characterization, and transfer to GMP manufacturing site.
  • Thermo Fisher Scientific
    R&D Project Manager Iii
    Thermo Fisher Scientific Jul 2017 - Present
    Waltham, Ma, Us
    Client facing Project Manager in Research and Development at a Contract Manufacturing Organization, dedicated to the development of softgel and gelatin based pharmaceuticals. Key aspects include:• Managing a diverse portfolio of 6-12 pharmaceutical development projects with an annual revenue of~3-4M across a wide variety of Rx and OTC pharmaceutical products, including cardiovascular, hormones, oncology, cough/cold, and proof of concept product development. • Guiding product development projects from inception to commercialization, including regulatory registration and clinical trial supply. • Lead project communications through entire development lifecycle including project kick-off, scheduled client meetings, client on-boarding, on-site hosting, and technical problem solving. Ensure communication is crisp for project status, issues, and targets through meeting minutes, timelines, and deliverable trackers.• Quarterback projects to drive project progression, anticipate issues, mitigate risk, and ensure the team is setup for success.• Administer multiple 3rd party vendors on behalf of clients for packaging, analytical testing, and secondary manufacturing to support project progression.• Serve as financial hub for R&D projects including, o Forecasting, tracking, and invoicing project milestones. o Managing project scope and developing proposals for additional work.o Administering client pass through cost for supplies, 3rd party vendors, shipping, and capital.• Active participation on site and global teams to improve ways of workingo Trained as a Process Manager for Practical Process Improvement (Lean / Operational Excellence), leading a training kaizen on “outside testing of raw materials”.o Site superuser for Changepoint, an enterprise wide project and portfolio management tool for planning, invoicing, resource allocation, and time tracking. o R&D representative for the global Voice of the Customer / Customer Engagement Management Team
  • Covance
    Senior Project Manager
    Covance Sep 2016 - Jul 2017
    Princeton, New Jersey, Us
    Lead a team of scientist and support staff to ensure client requirements and results are delivered successfully for a multi-faceted portfolio of non-GLP, GLP, GCP, and CLIA projects. Successful managed and guided 10-15 clients / programs through entire project life cycle of initiation, planning, execution, monitoring, and closeout. Central hub for stakeholder communications, serving as a conduit between clients, SME’s, clinical teams, and functional managers. Negotiate, plan, schedule, and direct resources to maximize efficiency, ensure timely completion, and minimize risk. Forecast, track, and invoice financial performance based on milestones and contractual obligations.
  • Covance
    Project Manager, Method Development
    Covance Aug 2015 - Sep 2016
    Princeton, New Jersey, Us
    Project management focused on developing and qualifying/validating new methods for targeted analysis in biological matrices. Plan, oversaw, reviewed, directed, and acted as a single point of accountability for all aspects of development projects including assay performance, regulatory compliance, and project administration. Reviewed study documentation to ensure accuracy and completeness. Mentored, trained staff, and acted as a technical resource for deployed methods. • Stabilized a short-lived peptide, solving an ISR investigation enabling development for a small virtual company of a therapeutic for controlled bladder release in individuals with neurological conditions. • Developed and validated trace level endogenous biomarkers of harm and inflammation for clinical studies.• Built and qualified methods to assess drug distribution in ocular tissues and trace levels in systemic exposure.
  • Gsk
    Investigator / Senior Scientist
    Gsk Jan 2013 - Aug 2015
    Brentford, Middlesex, Gb
    Managed, as a principle investigator and project team member, pharmacokinetic evaluation of novel pharmaceuticals. Trusted expert in DMPK for internal and external project teams. Successfully led and contributed to business initiatives in operations, quality improvement, innovation management, key process indicator development, and engagement (leadership, communication, and innovation).• Directed the DMPK effort to create and deploy methodology to support a pivotal study to evaluate a novel inhalation platform. Results provided insights into metabolite characterization, tissue distribution, and dose prediction directly enabling candidate selection and FTIH studies.• Spearheaded efforts to expand DMPK capabilities in drug distribution to enhance pharmacological understanding of dermatology studies, including pioneering scientific validations in GLP/GCP studies. • Established an inaugural “voice of the people” role on the PTS-DMPK executive board facilitating global communication while gaining insights into strategic planning, operations, decision making, and leadership.• Managed sample receipt and reconciliation for non-clinical and clinical studies.
  • Gsk
    Senior Scientist
    Gsk Mar 2011 - Dec 2012
    Brentford, Middlesex, Gb
    Project management of discovery DMPK programs to produce, review, and analyze in vitro and in vivo data to provide key insights into the ADME properties of drug candidate in HIV research. Total DMPK solution provided for internal and external experimental design, drug formulation, assay development, laboratory analysis, toxicokinetic assessment, and project team participation. Key project team milestones included demonstrating proof of concept animal efficacy models, Long Acting Parenteral formations development, FTIH, and two candidate selections.
  • Gsk
    Contract Senior Scientist
    Gsk Sep 2010 - Mar 2011
    Brentford, Middlesex, Gb
    One year contract to support In Vivo DMPK analysis in Drug Discovery. Offered permanent position as a result of restored project team confidence and improved quality in bioanalytical results. Initiated process improvements, work flow optimization, improved responsiveness, and increased accountability.
  • Gilead Sciences
    Associate Scientist I / Senior Research Associate Ii
    Gilead Sciences Apr 2006 - Aug 2010
    Foster City, Ca, Us
    Responsible scientist for entire life cycle of clinical bioanalytical projects, including quality management of external studies.
  • Metabolon
    Scientist
    Metabolon Jul 2003 - Feb 2006
    Morrisville, Nc, Us
    Created industry leading metabolomics platform for a successful biotech startup to characterize disease and identify biomarkers. Developed methodology, sample processing protocols, reference libraries, and data analysis workflow.
  • Paradigm Genetics
    Associate Scientist / Senior Assistant Scientist
    Paradigm Genetics Feb 2002 - Jul 2003
    Us
    Successful development and implementation of a metabolomic analytical and data analysis platform for analysis of biological systems.
  • Magellan Laboratories
    Chemist Ii
    Magellan Laboratories Nov 1998 - Feb 2002
    Technical expert in extractable and leachables analysis, who repeatedly developed, validated, and delivered quality results to ensure medical devices are safe for patients.

Chris Barringer (Mba, Pmp) Skills

Biosciences Management Pharmacology Data Analysis Pharmacokinetic Analysis Adme Metabolomics Assay Development And Validation Mass Spectrometry Automation Robotics Bioanalysis Instrument Repair Validation Regulatory Requirements Laboratory Construction Biotechnology Drug Metabolism Structural Chemistry Project Management Process Optimization Data Visualization Drug Discovery Laboratory Hplc Assay Development Glp Chemistry Chromatography Life Sciences Lc Ms Analytical Chemistry Biology Pharmacokinetics Cro Pharmaceutical Industry Liquid Chromatography Mass Spectrometry High Performance Liquid Chromatography Good Laboratory Practice Project Managment

Chris Barringer (Mba, Pmp) Education Details

  • North Carolina State University - College Of Management
    North Carolina State University - College Of Management
    Biosciences Management
  • University Of Maryland
    University Of Maryland
    Analytical & Environmental Chemistry
  • North Carolina State University
    North Carolina State University
    Chemistry

Frequently Asked Questions about Chris Barringer (Mba, Pmp)

What company does Chris Barringer (Mba, Pmp) work for?

Chris Barringer (Mba, Pmp) works for Fujifilm Biotechnologies

What is Chris Barringer (Mba, Pmp)'s role at the current company?

Chris Barringer (Mba, Pmp)'s current role is Quality Engineer, Program Manager.

What is Chris Barringer (Mba, Pmp)'s email address?

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What schools did Chris Barringer (Mba, Pmp) attend?

Chris Barringer (Mba, Pmp) attended North Carolina State University - College Of Management, University Of Maryland, North Carolina State University.

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What skills is Chris Barringer (Mba, Pmp) known for?

Chris Barringer (Mba, Pmp) has skills like Biosciences Management, Pharmacology, Data Analysis, Pharmacokinetic Analysis, Adme, Metabolomics, Assay Development And Validation, Mass Spectrometry, Automation, Robotics, Bioanalysis, Instrument Repair.

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