HPLC Scientist - ADTG

EurofinsLexington, MA
$31 - $34Onsite

About The Position

Contributes as part of a team of AD scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment. Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE (icIEF Maurice), iCE, CE-SDS (Maurice and PA800) - using established Test Methods, including associated protocol/report documentation and presentations. Conducts work in compliance with cGMP/GLP, safety and regulatory requirements. Responsible for working on other non-lab-based tasks from time to time if assigned. Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives. Demonstrate HPLC, UPLC and/or CE troubleshooting capabilities.

Requirements

  • Bachelor’s degree in Cell and Molecular Biology, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline with 2+ years of hands-on experience with HPLC/UPLC, including Reverse Phase (RP), Size Exclusion Chromatography (SEC), and/or Capillary Electrophoresis (CE) techniques.
  • Candidates with a Master’s degree in Cell and Molecular Biology, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline may be considered provided they have 6+ months of directly relevant internship or academic experience with HPLC/UPLC using RP, SEC, and/or CE methodologies.
  • Strong knowledge of principles and theory behind HPLC/UPLC/CE, including practical understanding of RP and/or SEC separations, and a basic understanding of industry practices and standards.
  • Demonstrated ability to learn new techniques, manage multiple tasks simultaneously, maintain accurate documentation, follow written procedures, and comply with company policies and regulatory requirements.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

  • Contributes as part of a team of AD scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment.
  • Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE (icIEF Maurice), iCE, CE-SDS (Maurice and PA800) - using established Test Methods, including associated protocol/report documentation and presentations.
  • Conducts work in compliance with cGMP/GLP, safety and regulatory requirements.
  • Responsible for working on other non-lab-based tasks from time to time if assigned.
  • Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives.
  • Demonstrate HPLC, UPLC and/or CE troubleshooting capabilities.

Benefits

  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
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