Peter Scott

Laboratory Instrument Specialist at ElevateBio
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Contact Information
us****@****om
(386) 825-5501
Location
Worcester, US
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John Peri-Okonny

Peter is one of the most energetic people I've had the pleasure of working with. His energy carries over and enables him to be able to build a rapport with everyone he meets. His quest for information and understanding of how to disect problems is highly appreciated - you know he will not give up until the problem is resolved, which makes you want go the extra mile for the solution to the problem. At the same time, he challenges you to be the best and think outside your comfortable box. I would not hesitate to team with Peter again because he brings out the best in people. January 18, 2010

Ziggy Waraszkiewicz

Peter helped lead the Process Analytical Technology (PAT) Team within the QA Laboratory Sciences Group at AstraZeneca. This team focused on developing and validating new analytical methods utilizing near-infrared spectroscopy as efficient non-destructive test methods for pharmaceutical products. His knowledge of the subject and ability to work well with other members of the Team was very important to the success of the Team.

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Credentials

  • 5S Certified
    Management & Strategy Institute
    Sep, 2020
    - Nov, 2024
  • Certified Pearl Specialist
    Cultured Pearl Associations of America, Inc.
    Aug, 2020
    - Nov, 2024

Experience

  • ElevateBio
    • United States
    • Biotechnology Research
    • 200 - 300 Employee
    • Laboratory Instrument Specialist
      • Sep 2023 - Present

      ● Act as the project lead for qualification of QC equipment and its associated software ● Design, execute, manage, and implement QC instrument/software qualification documents: URS, DQ, equipment IOQ, qualification summary report ● Own change controls specific to the qualification of QC instruments and its associated software ● Update the asset management database to reflect new assets, calibrations, preventative maintenances ● Author instrument operational SOPs… Show more ● Act as the project lead for qualification of QC equipment and its associated software ● Design, execute, manage, and implement QC instrument/software qualification documents: URS, DQ, equipment IOQ, qualification summary report ● Own change controls specific to the qualification of QC instruments and its associated software ● Update the asset management database to reflect new assets, calibrations, preventative maintenances ● Author instrument operational SOPs ● Coordinate/interface/host vendors on site Show less ● Act as the project lead for qualification of QC equipment and its associated software ● Design, execute, manage, and implement QC instrument/software qualification documents: URS, DQ, equipment IOQ, qualification summary report ● Own change controls specific to the qualification of QC instruments and its associated software ● Update the asset management database to reflect new assets, calibrations, preventative maintenances ● Author instrument operational SOPs… Show more ● Act as the project lead for qualification of QC equipment and its associated software ● Design, execute, manage, and implement QC instrument/software qualification documents: URS, DQ, equipment IOQ, qualification summary report ● Own change controls specific to the qualification of QC instruments and its associated software ● Update the asset management database to reflect new assets, calibrations, preventative maintenances ● Author instrument operational SOPs ● Coordinate/interface/host vendors on site Show less

  • Cytiva
    • Biotechnology Research
    • 700 & Above Employee
    • Analytical Development Scientist
      • Sep 2021 - Mar 2023

      ● Deviation, Change Control, Compliance documentation, IQ OP PQ ● Produced new SOPs, created work instructions/ technical writing/ updated existing procedures ● cGMP testing of stability samples ● Developing analytical testing methods ● Deviation, Change Control, Compliance documentation, IQ OP PQ ● Produced new SOPs, created work instructions/ technical writing/ updated existing procedures ● cGMP testing of stability samples ● Developing analytical testing methods

  • Chase Corporation
    • United States
    • Chemical Manufacturing
    • 1 - 100 Employee
    • Lead Analyst R&D
      • Jun 2020 - Jul 2021

      ● Oversaw the company's implementation of the 5S system (instrument calibration system, spare parts inventory control, scheduling, Kanban board, EH&S) ● Produced new SOPs, updated existing procedures, work instructions/ technical writing, safety procedures ● Oversaw all laboratory equipment and instruments, IQ, OQ, PQ ● Performed all safety/facilities inspections, hazmat waste management ● Oversaw the company's implementation of the 5S system (instrument calibration system, spare parts inventory control, scheduling, Kanban board, EH&S) ● Produced new SOPs, updated existing procedures, work instructions/ technical writing, safety procedures ● Oversaw all laboratory equipment and instruments, IQ, OQ, PQ ● Performed all safety/facilities inspections, hazmat waste management

  • Waters Corporation
    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Evaluation Engineer II
      • Oct 2008 - Jan 2020

      - Evaluated quality of software and hardware products for use in GMP labs - Validated software and instruments for testing - Developed test cases: software and hardware evaluation - Identified and verified defects - Strong communication skills of scientific data for presentations and reports. - Ensured compliance with company policies and procedures - Trained new resources - Tested for GMP and GLP compliance - Innovated new ideas, processes and technologies for the… Show more - Evaluated quality of software and hardware products for use in GMP labs - Validated software and instruments for testing - Developed test cases: software and hardware evaluation - Identified and verified defects - Strong communication skills of scientific data for presentations and reports. - Ensured compliance with company policies and procedures - Trained new resources - Tested for GMP and GLP compliance - Innovated new ideas, processes and technologies for the advancement of the company Show less - Evaluated quality of software and hardware products for use in GMP labs - Validated software and instruments for testing - Developed test cases: software and hardware evaluation - Identified and verified defects - Strong communication skills of scientific data for presentations and reports. - Ensured compliance with company policies and procedures - Trained new resources - Tested for GMP and GLP compliance - Innovated new ideas, processes and technologies for the… Show more - Evaluated quality of software and hardware products for use in GMP labs - Validated software and instruments for testing - Developed test cases: software and hardware evaluation - Identified and verified defects - Strong communication skills of scientific data for presentations and reports. - Ensured compliance with company policies and procedures - Trained new resources - Tested for GMP and GLP compliance - Innovated new ideas, processes and technologies for the advancement of the company Show less

  • Avatar Pharmaceutical Services
    • Chemist III
      • Apr 2007 - Aug 2008

      Developed and validated analytical methods to suit formulation needs. Performed stability testing of DNA, RNA, protein, and oligonucleotide based drug products. IQ, OQ, and PQ of laboratory equipment, including HPLC, UPLC, FTIR, CE and dissolution apparatus.  Trained analysts on the proper operation and techniques involved with cGMP testing.  Developed HPLC methods based on the Japanese pharmacopoeia.  Purchased and qualified new HPLC systems for the chemistry labs. Developed and validated analytical methods to suit formulation needs. Performed stability testing of DNA, RNA, protein, and oligonucleotide based drug products. IQ, OQ, and PQ of laboratory equipment, including HPLC, UPLC, FTIR, CE and dissolution apparatus.  Trained analysts on the proper operation and techniques involved with cGMP testing.  Developed HPLC methods based on the Japanese pharmacopoeia.  Purchased and qualified new HPLC systems for the chemistry labs.

  • CIS bio international
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Chemist III
      • Aug 2005 - Feb 2007

      Release testing for raw materials and radiopharmaceutical products, iodine-131 and technetium-99 using HPLC. Trained analysts in HPLC and software (Empower) usage. Wrote deviations and investigations. Release testing for raw materials and radiopharmaceutical products, iodine-131 and technetium-99 using HPLC. Trained analysts in HPLC and software (Empower) usage. Wrote deviations and investigations.

  • AstraZeneca
    • United Kingdom
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Senior Scientist
      • Nov 1998 - Aug 2005

      Responsible for development of analytical methods, evaluation of new technologies and implementation of Process Analytical Technology to improve quality and production of solid oral dosage forms.  Implement dissolution testing program with systems installed, qualified, calibrated, SOPs written, analyst trained, and methods transferred, within first two quarters of starting.  Saved company cost of vendor calibration by taking over calibration responsibility internally.  Created… Show more Responsible for development of analytical methods, evaluation of new technologies and implementation of Process Analytical Technology to improve quality and production of solid oral dosage forms.  Implement dissolution testing program with systems installed, qualified, calibrated, SOPs written, analyst trained, and methods transferred, within first two quarters of starting.  Saved company cost of vendor calibration by taking over calibration responsibility internally.  Created standard operating procedures for use in electronic signature/ electronic records compliance with 21CFR part11.  Developed cutting edge PAT methods correlating off-line NIR to HPLC results using chemometrics and Simca-P multivariate mathematical techniques.  Established, calibrated, and managed dissolution testing systems for site. Show less Responsible for development of analytical methods, evaluation of new technologies and implementation of Process Analytical Technology to improve quality and production of solid oral dosage forms.  Implement dissolution testing program with systems installed, qualified, calibrated, SOPs written, analyst trained, and methods transferred, within first two quarters of starting.  Saved company cost of vendor calibration by taking over calibration responsibility internally.  Created… Show more Responsible for development of analytical methods, evaluation of new technologies and implementation of Process Analytical Technology to improve quality and production of solid oral dosage forms.  Implement dissolution testing program with systems installed, qualified, calibrated, SOPs written, analyst trained, and methods transferred, within first two quarters of starting.  Saved company cost of vendor calibration by taking over calibration responsibility internally.  Created standard operating procedures for use in electronic signature/ electronic records compliance with 21CFR part11.  Developed cutting edge PAT methods correlating off-line NIR to HPLC results using chemometrics and Simca-P multivariate mathematical techniques.  Established, calibrated, and managed dissolution testing systems for site. Show less

  • US Army
    • United States
    • Armed Forces
    • 700 & Above Employee
    • Combat Engineer SPC-4 of the Persian Gulf War
      • Dec 1990 - Dec 1991

      Activated for the Persian Gulf War I with 181 Engineers, Whitman Massachusetts We rebuilt and enhanced the roadway infrastructure of the Kingdom of Saudi Arabia, Interacted with local nationals, designed and constructed large scale construction projects. Army Service Ribbon, Army Commendation Medal, South West Asia Service Medal, Army Lapel Button, National Defense Service Ribbon, Kuwait Liberation Medal (Saudi), Kuwait Liberation Medal (Kuwait), Expert Badge M16… Show more Activated for the Persian Gulf War I with 181 Engineers, Whitman Massachusetts We rebuilt and enhanced the roadway infrastructure of the Kingdom of Saudi Arabia, Interacted with local nationals, designed and constructed large scale construction projects. Army Service Ribbon, Army Commendation Medal, South West Asia Service Medal, Army Lapel Button, National Defense Service Ribbon, Kuwait Liberation Medal (Saudi), Kuwait Liberation Medal (Kuwait), Expert Badge M16 Rifle, Expert Badge Hand Grenade Show less Activated for the Persian Gulf War I with 181 Engineers, Whitman Massachusetts We rebuilt and enhanced the roadway infrastructure of the Kingdom of Saudi Arabia, Interacted with local nationals, designed and constructed large scale construction projects. Army Service Ribbon, Army Commendation Medal, South West Asia Service Medal, Army Lapel Button, National Defense Service Ribbon, Kuwait Liberation Medal (Saudi), Kuwait Liberation Medal (Kuwait), Expert Badge M16… Show more Activated for the Persian Gulf War I with 181 Engineers, Whitman Massachusetts We rebuilt and enhanced the roadway infrastructure of the Kingdom of Saudi Arabia, Interacted with local nationals, designed and constructed large scale construction projects. Army Service Ribbon, Army Commendation Medal, South West Asia Service Medal, Army Lapel Button, National Defense Service Ribbon, Kuwait Liberation Medal (Saudi), Kuwait Liberation Medal (Kuwait), Expert Badge M16 Rifle, Expert Badge Hand Grenade Show less

Education

  • Fort Leonard Wood, MO
    Advanced Individual Training, Combat Engineering
  • University of Maine
    Bachelor of Science - BS, Chemistry
  • Waterville High school
  • Fort Leonard Wood
    Army Basic Training, E-3

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